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xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">February 2012</prism:coverDisplayDate><prism:volume xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">18</prism:volume><prism:number xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1</prism:number><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">132</prism:endingPage><image rdf:resource="http://onlinelibrary.wiley.com/store/10.1111/srt.2011.18.issue-1/asset/cover.gif?v=1&amp;s=411064623c24b8c195238a5fc8ccb880accf1c95"/><items><rdf:Seq><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00606.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00595.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00593.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00604.x"/><rdf:li 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rdf:resource="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00543.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00527.x"/><rdf:li rdf:resource="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00528.x"/></rdf:Seq></items></channel><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00606.x" xmlns="http://purl.org/rss/1.0/"><title>The vascular features of psoriatic skin: imaging using in vivo confocal laser scanning microscopy</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00606.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The vascular features of psoriatic skin: imaging using in vivo confocal laser scanning microscopy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Dai Hui</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Xu Ai-E</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-22T20:39:19.602573-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00606.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00606.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00606.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00595.x" xmlns="http://purl.org/rss/1.0/"><title>Discrimination of basal cell carcinoma from benign lesions based on extraction of ulcer features in polarized-light dermoscopy images</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00595.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Discrimination of basal cell carcinoma from benign lesions based on extraction of ulcer features in polarized-light dermoscopy images</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Serkan Kefel</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Pelin Guvenc</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Robert LeAnder</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sherea M. Stricklin</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">William V. Stoecker</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-22T20:38:22.586892-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00595.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00595.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00595.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt595-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Ulcers are frequently visible in magnified, cross-polarized, dermoscopy images of basal cell carcinoma. An ulcer without a history of trauma, a so-called ‘atraumatic’ ulcer, is an important sign of basal cell carcinoma, the most common skin cancer. Distinguishing such ulcers from similar features found in benign lesions is challenging. In this research, color and texture features of ulcers are analyzed to discriminate basal cell carcinoma from benign lesions.</p></div></div><div class="section" id="srt595-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Ulcers in polarized-light dermoscopy images of 49 biopsy-proven basal cell carcinomas were identified and manually selected. For 153 polarized-light dermoscopy images of benign lesions, those areas that most closely mimicked ulcers were similarly selected. Fifteen measures were analyzed over the areas of ulcers and ulcer mimics. Six of those measures were texture measures: energy, variance, smoothness, skewness, uniformity, and entropy. Nine of those measures were color measures: relative measures of red, green, and blue; chromaticity of red, green, and blue; and the ratios blue-to-green, blue-to-red, and green-to-red.</p></div></div><div class="section" id="srt595-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>A back-propagation artificial neural network was able to discriminate most of the basal cell carcinoma from benign lesions, with an area under the ROC curve as high as 92.46%, using color and texture features of ulcer areas.</p></div></div><div class="section" id="srt595-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Separation of basal cell carcinoma from benign cutaneous lesions using image analysis techniques applied to ulcers is feasible. As ulcers are a critical feature in malignant lesions, this finding may have application in the automatic detection of basal cell carcinoma.</p></div></div>]]></content:encoded><description>BackgroundUlcers are frequently visible in magnified, cross-polarized, dermoscopy images of basal cell carcinoma. An ulcer without a history of trauma, a so-called ‘atraumatic’ ulcer, is an important sign of basal cell carcinoma, the most common skin cancer. Distinguishing such ulcers from similar features found in benign lesions is challenging. In this research, color and texture features of ulcers are analyzed to discriminate basal cell carcinoma from benign lesions.MethodsUlcers in polarized-light dermoscopy images of 49 biopsy-proven basal cell carcinomas were identified and manually selected. For 153 polarized-light dermoscopy images of benign lesions, those areas that most closely mimicked ulcers were similarly selected. Fifteen measures were analyzed over the areas of ulcers and ulcer mimics. Six of those measures were texture measures: energy, variance, smoothness, skewness, uniformity, and entropy. Nine of those measures were color measures: relative measures of red, green, and blue; chromaticity of red, green, and blue; and the ratios blue-to-green, blue-to-red, and green-to-red.ResultsA back-propagation artificial neural network was able to discriminate most of the basal cell carcinoma from benign lesions, with an area under the ROC curve as high as 92.46%, using color and texture features of ulcer areas.ConclusionSeparation of basal cell carcinoma from benign cutaneous lesions using image analysis techniques applied to ulcers is feasible. As ulcers are a critical feature in malignant lesions, this finding may have application in the automatic detection of basal cell carcinoma.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00593.x" xmlns="http://purl.org/rss/1.0/"><title>FluxEXPLORER: a new high-speed laser Doppler imaging system for the assessment of burn injuries</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00593.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">FluxEXPLORER: a new high-speed laser Doppler imaging system for the assessment of burn injuries</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Paolo Erba</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Daniel Espinoza</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nathalie Koch</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Thierry Christen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Alexandre Serov</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wassim Raffoul</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-15T03:40:37.838893-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00593.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00593.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00593.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt593-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Deep burn assessment made by clinical evaluation has an accuracy varying between 60% and 80% and will determine if a burn injury will need tangential excision and skin grafting or if it will be able to heal spontaneously. Laser Doppler Imaging (LDI) techniques allow an improved burn depth assessment but their use is limited by the time-consuming image acquisition which may take up to 6 min per image.</p></div></div><div class="section" id="srt593-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>To evaluate the effectiveness and reliability of a newly developed full-field LDI technology, 15 consecutive patients presenting with intermediate depth burns were assessed both clinically and by FluxExplorer LDI technology. Comparison between the two methods of assessment was carried out.</p></div></div><div class="section" id="srt593-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Image acquisition was done within 6 s. FluxEXPLORER LDI technology achieved a significantly improved accuracy of burn depth assessment compared to the clinical judgement performed by board certified plastic and reconstructive surgeons (<em>P</em> &lt; 0.05, 93% of correctly assessed burns injuries vs. 80% for clinical assessment).</p></div></div><div class="section" id="srt593-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Technological improvements of LDI technology leading to a decreased image acquisition time and reliable burn depth assessment allow the routine use of such devices in the acute setting of burn care without interfering with the patient's treatment. Rapid and reliable LDI technology may assist clinicians in burn depth assessment and may limit the morbidity of burn patients through a minimization of the area of surgical debridement. Future technological improvements allowing the miniaturization of the device will further ease its clinical application.</p></div></div>]]></content:encoded><description>BackgroundDeep burn assessment made by clinical evaluation has an accuracy varying between 60% and 80% and will determine if a burn injury will need tangential excision and skin grafting or if it will be able to heal spontaneously. Laser Doppler Imaging (LDI) techniques allow an improved burn depth assessment but their use is limited by the time-consuming image acquisition which may take up to 6 min per image.MethodsTo evaluate the effectiveness and reliability of a newly developed full-field LDI technology, 15 consecutive patients presenting with intermediate depth burns were assessed both clinically and by FluxExplorer LDI technology. Comparison between the two methods of assessment was carried out.ResultsImage acquisition was done within 6 s. FluxEXPLORER LDI technology achieved a significantly improved accuracy of burn depth assessment compared to the clinical judgement performed by board certified plastic and reconstructive surgeons (P &lt; 0.05, 93% of correctly assessed burns injuries vs. 80% for clinical assessment).ConclusionTechnological improvements of LDI technology leading to a decreased image acquisition time and reliable burn depth assessment allow the routine use of such devices in the acute setting of burn care without interfering with the patient's treatment. Rapid and reliable LDI technology may assist clinicians in burn depth assessment and may limit the morbidity of burn patients through a minimization of the area of surgical debridement. Future technological improvements allowing the miniaturization of the device will further ease its clinical application.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00604.x" xmlns="http://purl.org/rss/1.0/"><title>Multi-directional in vivo tensile skin stiffness measurement for the design of a reproducible tensile strain elastography protocol</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00604.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Multi-directional in vivo tensile skin stiffness measurement for the design of a reproducible tensile strain elastography protocol</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Louise Coutts</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jeffrey Bamber</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Naomi Miller</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-06T23:51:52.916837-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00604.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00604.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00604.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt604-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background/Aims</h3><div class="para"><p>Elastography is a promising new medical imaging modality, displaying spatial distribution of biomechanical properties such as local tissue strain response to an applied stress. To develop a reproducible test protocol for skin elastography, the effect of various parameters on skin stiffness measurements was investigated.</p></div></div><div class="section" id="srt604-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>The parameters investigated were: history of skin loading before test loading (preconditioning), direction of test loading (anisotropy) and posture (pre-stress). If a sample of skin is loaded, its stiffness will temporarily change. Finally, the reproducibility of skin stiffness and anisotropy measurements, using the developed techniques, was investigated.</p></div></div><div class="section" id="srt604-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>By measuring how the stiffness changed with different time delays between loading cycles, the time required for healthy skin to return to its original pre-loaded state was in the region of 125 s. A second finding, which supports and extends previous work, was that skin stiffness varied with direction, by an approximate factor of 2, and that anisotropy was less apparent with preconditioned skin than non-preconditioned skin. Study of the effect of posture showed that care needs to be taken over which stiffness measure is used. For example, measurement of the load at a given displacement was found to be highly dependent on posture, whereas measurement of the phase III stiffness was independent of posture.</p></div></div><div class="section" id="srt604-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>It was shown that when the measurement variables and methods of analysis were standardised, skin stiffness could be measured reproducibly enough to distinguish</p></div><div class="para"><p>between the stiffest and softest directions, and that these methods allowed formation of skin elastograms free from confounding influences.</p></div></div>]]></content:encoded><description>Background/AimsElastography is a promising new medical imaging modality, displaying spatial distribution of biomechanical properties such as local tissue strain response to an applied stress. To develop a reproducible test protocol for skin elastography, the effect of various parameters on skin stiffness measurements was investigated.MethodsThe parameters investigated were: history of skin loading before test loading (preconditioning), direction of test loading (anisotropy) and posture (pre-stress). If a sample of skin is loaded, its stiffness will temporarily change. Finally, the reproducibility of skin stiffness and anisotropy measurements, using the developed techniques, was investigated.ResultsBy measuring how the stiffness changed with different time delays between loading cycles, the time required for healthy skin to return to its original pre-loaded state was in the region of 125 s. A second finding, which supports and extends previous work, was that skin stiffness varied with direction, by an approximate factor of 2, and that anisotropy was less apparent with preconditioned skin than non-preconditioned skin. Study of the effect of posture showed that care needs to be taken over which stiffness measure is used. For example, measurement of the load at a given displacement was found to be highly dependent on posture, whereas measurement of the phase III stiffness was independent of posture.ConclusionIt was shown that when the measurement variables and methods of analysis were standardised, skin stiffness could be measured reproducibly enough to distinguishbetween the stiffest and softest directions, and that these methods allowed formation of skin elastograms free from confounding influences.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00611.x" xmlns="http://purl.org/rss/1.0/"><title>Use of digital infrared imaging in the assessment of childhood psoriasis</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00611.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Use of digital infrared imaging in the assessment of childhood psoriasis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Claudio Castillo-Martínez</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rodrigo Valdes-Rodríguez</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Eleazar S. Kolosovas-Machuca</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Benjamín Moncada</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Francisco J. González</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-31T05:17:13.607724-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00611.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00611.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00611.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00599.x" xmlns="http://purl.org/rss/1.0/"><title>SkinExplorerTM: a new high-tech platform to interact inside the skin by immersive virtual 3D cutaneous environment</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00599.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">SkinExplorerTM: a new high-tech platform to interact inside the skin by immersive virtual 3D cutaneous environment</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. D. Vazquez-Duchêne</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">P. Kraemer</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">N. Saugnier</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">B. Levy</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. Mine</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. Jeanmaire</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">O. Freis</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G. Pauly</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Rathjens</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-24T23:19:19.115299-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00599.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00599.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00599.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt599-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>The confocal laser scanning microscope allows performing acquisition of several histological sections with precise visual morphological landmarks and their reconstruction. A powerful and modern confocal microscope enables to quickly reconstruct virtual 3D models.</p></div></div><div class="section" id="srt599-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Objective</h3><div class="para"><p>The main goal was to develop a new platform to reconstruct complex mosaic serial data, interact with it in an immersive 3D environment, and give to the observers a feeling of ‘presence’ inside the skin.</p></div></div><div class="section" id="srt599-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Method</h3><div class="para"><p>We have developed novel methods that transform the data into alternative representation, well-suited to explore cutaneous structures in detail and to observe fields of data from different points of view. This new way of data reconstruction in volume requires optimization of intensities, automatic matching algorithms and depth alignment.</p></div></div><div class="section" id="srt599-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results and conclusion</h3><div class="para"><p>The new platform – SkinExplorer<sup>TM</sup> evolves as a 3D exploration prototype. This technology provides an immersive virtual environment to explore cutaneous microstructures. Several serial histological sections can be matched by stacks, aligned in depth by sections and merged together to be visualized as a whole. All these time-consuming steps have been dramatically speed-up using rapid image processing. The advantages of using virtual reality technologies such as the ones used in the SkinExplorer<sup>TM</sup> platform are automatic matching, precise alignment, better data perception, lower memory requirement, and higher quantity of simultaneously displayed data. This platform can render volumetric data and isosurfaces, separately or both at the same time. Lighting and depth perception are enhanced using ‘Sphere Mapping’, ‘Ambient Occlusion’, and ‘Halo’ methods when displaying iso-surfacic volume models with high complexity depth. The assets of the platform are to interpret complex three-dimensional data, to observe and explore 3D virtual models, and to show effects of cosmetic treatments.</p></div></div>]]></content:encoded><description>BackgroundThe confocal laser scanning microscope allows performing acquisition of several histological sections with precise visual morphological landmarks and their reconstruction. A powerful and modern confocal microscope enables to quickly reconstruct virtual 3D models.ObjectiveThe main goal was to develop a new platform to reconstruct complex mosaic serial data, interact with it in an immersive 3D environment, and give to the observers a feeling of ‘presence’ inside the skin.MethodWe have developed novel methods that transform the data into alternative representation, well-suited to explore cutaneous structures in detail and to observe fields of data from different points of view. This new way of data reconstruction in volume requires optimization of intensities, automatic matching algorithms and depth alignment.Results and conclusionThe new platform – SkinExplorerTM evolves as a 3D exploration prototype. This technology provides an immersive virtual environment to explore cutaneous microstructures. Several serial histological sections can be matched by stacks, aligned in depth by sections and merged together to be visualized as a whole. All these time-consuming steps have been dramatically speed-up using rapid image processing. The advantages of using virtual reality technologies such as the ones used in the SkinExplorerTM platform are automatic matching, precise alignment, better data perception, lower memory requirement, and higher quantity of simultaneously displayed data. This platform can render volumetric data and isosurfaces, separately or both at the same time. Lighting and depth perception are enhanced using ‘Sphere Mapping’, ‘Ambient Occlusion’, and ‘Halo’ methods when displaying iso-surfacic volume models with high complexity depth. The assets of the platform are to interpret complex three-dimensional data, to observe and explore 3D virtual models, and to show effects of cosmetic treatments.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00594.x" xmlns="http://purl.org/rss/1.0/"><title>Quantitative color assessment of dermoscopy images using perceptible color regions</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00594.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Quantitative color assessment of dermoscopy images using perceptible color regions</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gunwoo Lee</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Onseok Lee</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sunup Park</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jongsub Moon</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Chilhwan Oh</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-24T23:10:21.048295-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00594.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00594.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00594.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt594-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Dermoscopy is a non-invasive <em>in vivo</em> skin imaging technique that assists dermatologists in diagnosing melanoma. However, the use of dermoscopy for diagnosis requires extensive training since this approach often provides extremely complex and subjective information. The presence of an imperceptible color difference in dermoscopy images is one of the serious problems associated with the use of this technique. This imperceptible color difference leads to inaccurate lesion extraction at the borders and hinders the assessment of lesion features. Therefore, objective and quantitative assessment based on perceptible color differences is important for the diagnosis of melanoma using dermoscopy.</p></div></div><div class="section" id="srt594-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>In this study, we developed a method for assessing colors in a lesion. Twenty-seven perceptible color regions based on the multi-thresholding method in each color channel were constructed, and dominant color region (DCR), bluish dominant region (BDR), and the number of colors were assessed as three diagnostic parameters from these perceptible color regions on 150 dermoscopy images.</p></div></div><div class="section" id="srt594-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results/Conclusion</h3><div class="para"><p>Diagnostic accuracy was calculated by combination of three diagnostic parameters derived from DCR, BDR, and the number of colors. Diagnostic accuracy with 73.33% sensitivity and 90.67% specificity was obtained in case of positive features in more than two parameters.</p></div></div>]]></content:encoded><description>BackgroundDermoscopy is a non-invasive in vivo skin imaging technique that assists dermatologists in diagnosing melanoma. However, the use of dermoscopy for diagnosis requires extensive training since this approach often provides extremely complex and subjective information. The presence of an imperceptible color difference in dermoscopy images is one of the serious problems associated with the use of this technique. This imperceptible color difference leads to inaccurate lesion extraction at the borders and hinders the assessment of lesion features. Therefore, objective and quantitative assessment based on perceptible color differences is important for the diagnosis of melanoma using dermoscopy.MethodsIn this study, we developed a method for assessing colors in a lesion. Twenty-seven perceptible color regions based on the multi-thresholding method in each color channel were constructed, and dominant color region (DCR), bluish dominant region (BDR), and the number of colors were assessed as three diagnostic parameters from these perceptible color regions on 150 dermoscopy images.Results/ConclusionDiagnostic accuracy was calculated by combination of three diagnostic parameters derived from DCR, BDR, and the number of colors. Diagnostic accuracy with 73.33% sensitivity and 90.67% specificity was obtained in case of positive features in more than two parameters.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00610.x" xmlns="http://purl.org/rss/1.0/"><title>Computerised image analysis of vitiligo lesion: evaluation using manually defined lesion areas</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00610.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Computerised image analysis of vitiligo lesion: evaluation using manually defined lesion areas</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hermawan Nugroho</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Hani Ahmad Fadzil</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Norashikin Shamsudin</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. H. Hussein</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-11T05:28:55.301204-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00610.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00610.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00610.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt610-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Vitiligo is a cutaneous pigmentary disorder characterized by depigmented macules and patches that result from loss of epidermal melanocytes. Physician evaluates the efficacy of treatment by comparing the extent of vitiligo lesions before and after treatment based on the overall visual impression of the treatment response. This method is called the physician's global assessment (PGA) which is subjective. In this article, we present an innovative digital image processing method to determine vitiligo lesion area in an objective manner.</p></div></div><div class="section" id="srt610-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Method</h3><div class="para"><p>The digital method uses Independent Component Analysis (ICA) to generate melanin-based images representing skin areas due to melanin followed by Region Growing process to segment vitiligo lesion from normal skin.</p></div></div><div class="section" id="srt610-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Based on 41 digital images of vitiligo lesions taken from 18 patients, the proposed method achieved sensitivities of 0.9105 ± 0.0161, specificities of 0.9973 ± 0.0009 and accuracies of 0.9901 ± 0.0028 at 95% confidence level.</p></div></div><div class="section" id="srt610-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>With the proposed method, physicians are able to assess vitiligo treatment efficacies objectively.</p></div></div>]]></content:encoded><description>BackgroundVitiligo is a cutaneous pigmentary disorder characterized by depigmented macules and patches that result from loss of epidermal melanocytes. Physician evaluates the efficacy of treatment by comparing the extent of vitiligo lesions before and after treatment based on the overall visual impression of the treatment response. This method is called the physician's global assessment (PGA) which is subjective. In this article, we present an innovative digital image processing method to determine vitiligo lesion area in an objective manner.MethodThe digital method uses Independent Component Analysis (ICA) to generate melanin-based images representing skin areas due to melanin followed by Region Growing process to segment vitiligo lesion from normal skin.ResultsBased on 41 digital images of vitiligo lesions taken from 18 patients, the proposed method achieved sensitivities of 0.9105 ± 0.0161, specificities of 0.9973 ± 0.0009 and accuracies of 0.9901 ± 0.0028 at 95% confidence level.ConclusionWith the proposed method, physicians are able to assess vitiligo treatment efficacies objectively.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00598.x" xmlns="http://purl.org/rss/1.0/"><title>Skin wrinkling morphology changes suddenly in the early 30s</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00598.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Skin wrinkling morphology changes suddenly in the early 30s</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Osamu Kuwazuru</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kukizo Miyamoto</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nobuhiro Yoshikawa</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Shuhei Imayama</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-11T03:40:29.791403-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00598.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00598.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00598.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt598-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background/purpose</h3><div class="para"><p>Does the morphology of wrinkles alter gradually with aging or suddenly at a certain age? On the basis of the theoretic wrinkle simulation of ideal skin, we have suggested that the wrinkle morphology suddenly changes from stratum corneum wrinkling to epidermis wrinkling; the former induces shallow fine furrows, and the latter induces deep prominent wrinkles. To examine the existence of drastic change in wrinkling morphology, we developed a new measurement system for facial skin wrinkling test.</p></div></div><div class="section" id="srt598-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>The mechanical compression test of facial skin was carried out for 102 Japanese women aged 25–56 years. The test was performed on the right temple area skin, and the area of wrinkles induced by the compression was measured using a digital video camera. The rate of increase in wrinkle area during compression was defined as the skin wrinkling rate, and it was calculated for all subjects automatically by image processing.</p></div></div><div class="section" id="srt598-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>The test results showed that the skin wrinkling rate underwent a step increase at the age 33, which means that the wrinkling morphologies of young and old skins are completely different, and so it changes suddenly in the early 30s.</p></div></div><div class="section" id="srt598-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>A new skin measurement system was developed to validate our theory of wrinkle formation mechanism with aging. The results demonstrated the wrinkling morphology changes suddenly at early 30s.</p></div></div>]]></content:encoded><description>Background/purposeDoes the morphology of wrinkles alter gradually with aging or suddenly at a certain age? On the basis of the theoretic wrinkle simulation of ideal skin, we have suggested that the wrinkle morphology suddenly changes from stratum corneum wrinkling to epidermis wrinkling; the former induces shallow fine furrows, and the latter induces deep prominent wrinkles. To examine the existence of drastic change in wrinkling morphology, we developed a new measurement system for facial skin wrinkling test.MethodsThe mechanical compression test of facial skin was carried out for 102 Japanese women aged 25–56 years. The test was performed on the right temple area skin, and the area of wrinkles induced by the compression was measured using a digital video camera. The rate of increase in wrinkle area during compression was defined as the skin wrinkling rate, and it was calculated for all subjects automatically by image processing.ResultsThe test results showed that the skin wrinkling rate underwent a step increase at the age 33, which means that the wrinkling morphologies of young and old skins are completely different, and so it changes suddenly in the early 30s.ConclusionA new skin measurement system was developed to validate our theory of wrinkle formation mechanism with aging. The results demonstrated the wrinkling morphology changes suddenly at early 30s.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00592.x" xmlns="http://purl.org/rss/1.0/"><title>Influence of hypodermic needle dimensions on subcutaneous injection delivery – a pig study of injection deposition evaluated by CT scanning, histology, and backflow</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00592.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Influence of hypodermic needle dimensions on subcutaneous injection delivery – a pig study of injection deposition evaluated by CT scanning, histology, and backflow</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kezia Ann Præstmark Juul</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Henrik Bengtsson</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bente Eyving</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jonas Kildegaard</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Steffen Lav</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mette Poulsen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jørgen Serup</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bente Stallknecht</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-11T03:23:08.802781-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00592.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00592.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00592.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt592-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Thinner and shorter needles for subcutaneous administration are continuously developed. Previous studies have shown that a thinner needle causes fewer occurrences of painful needle insertions and that a shorter needle decreases the occurrence of painful intramuscular injections. However, little is known about local drug delivery in relation to needle length and thickness. This study aimed to compare deposition depth and backflow from three hypodermic needles of 3 mm 34G (0.19 mm), 5 mm 32G (0.23 mm), and 8 mm 30G (0.30 mm) in length and thickness.</p></div></div><div class="section" id="srt592-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p><em>Ex vivo</em> experiments were carried out on pigs, in neck tissue comparable to human skin at typical injection sites. Six pigs were included and a total of 72 randomized injections were given, i.e. 24 subcutaneous injections given with each needle type. Accordingly, 400 μL was injected including 70% NovoRapid<sup>®</sup> (Novo Nordisk A/S, Bagsvμrd, Denmark) and 30% Xenetix<sup>®</sup> (Guerbet, Villepinte, France) contrast including 1 mg/mL Alcian blue. Surgical biopsies of injection sites were sampled and computer topographic (CT)-scanned in 3D to assess deposition and local distribution. Biopsies were prepared and stained to evaluate deposition in comparison to the CT-scanning findings. The backflow of each injection was collected with filter paper. The blue stains of filter paper were digitized and volume estimated by software calculation vs. control staining.</p></div></div><div class="section" id="srt592-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>CT-scanning (<em>n</em> = 57) and histology (<em>n</em> = 10) showed that, regardless of injection depth, the bulk of the injection was in the subcutaneous tissue and did not propagate from subcutis into dermis. With the 8 mm 30G needle all injections apart from one intramuscular injection were located in the subcutaneous layer. The volume depositions peaked in 4–5 mm depth for the 3 mm 34G needle, in 5–6 mm depth for the 5 mm 32G needle, and in 9–10 mm depth for the 8 mm 30G needle. In general, injection depositions evaluated by histology and CT-scans compared well for the individual biopsies. The amount of backflow (<em>n</em> = 69) from the 3 mm 34G needle was smaller (<em>P</em> &lt; 0.05) as compared to the 5 mm 32G and the 8 mm 30G needles. Analysis showed a correlation between backflow and the needle's outer dimension with the needle diameter being the pivotal parameter. Furthermore, CT-scanning and histology confirmed that local propagation of the injection and final distribution followed a route of less mechanical resistance as determined by connective tissue barriers preset in the site of injection.</p></div></div><div class="section" id="srt592-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Needles as short as 3 mm efficiently delivered injections into the subcutaneous target. The amount of backflow was smaller with thinner needles. Local distribution was variable and determined by mechanical barriers preset in the tissue. CT-scans and histology were concordant.</p></div></div>]]></content:encoded><description>BackgroundThinner and shorter needles for subcutaneous administration are continuously developed. Previous studies have shown that a thinner needle causes fewer occurrences of painful needle insertions and that a shorter needle decreases the occurrence of painful intramuscular injections. However, little is known about local drug delivery in relation to needle length and thickness. This study aimed to compare deposition depth and backflow from three hypodermic needles of 3 mm 34G (0.19 mm), 5 mm 32G (0.23 mm), and 8 mm 30G (0.30 mm) in length and thickness.MethodsEx vivo experiments were carried out on pigs, in neck tissue comparable to human skin at typical injection sites. Six pigs were included and a total of 72 randomized injections were given, i.e. 24 subcutaneous injections given with each needle type. Accordingly, 400 μL was injected including 70% NovoRapid® (Novo Nordisk A/S, Bagsvμrd, Denmark) and 30% Xenetix® (Guerbet, Villepinte, France) contrast including 1 mg/mL Alcian blue. Surgical biopsies of injection sites were sampled and computer topographic (CT)-scanned in 3D to assess deposition and local distribution. Biopsies were prepared and stained to evaluate deposition in comparison to the CT-scanning findings. The backflow of each injection was collected with filter paper. The blue stains of filter paper were digitized and volume estimated by software calculation vs. control staining.ResultsCT-scanning (n = 57) and histology (n = 10) showed that, regardless of injection depth, the bulk of the injection was in the subcutaneous tissue and did not propagate from subcutis into dermis. With the 8 mm 30G needle all injections apart from one intramuscular injection were located in the subcutaneous layer. The volume depositions peaked in 4–5 mm depth for the 3 mm 34G needle, in 5–6 mm depth for the 5 mm 32G needle, and in 9–10 mm depth for the 8 mm 30G needle. In general, injection depositions evaluated by histology and CT-scans compared well for the individual biopsies. The amount of backflow (n = 69) from the 3 mm 34G needle was smaller (P &lt; 0.05) as compared to the 5 mm 32G and the 8 mm 30G needles. Analysis showed a correlation between backflow and the needle's outer dimension with the needle diameter being the pivotal parameter. Furthermore, CT-scanning and histology confirmed that local propagation of the injection and final distribution followed a route of less mechanical resistance as determined by connective tissue barriers preset in the site of injection.ConclusionNeedles as short as 3 mm efficiently delivered injections into the subcutaneous target. The amount of backflow was smaller with thinner needles. Local distribution was variable and determined by mechanical barriers preset in the tissue. CT-scans and histology were concordant.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00600.x" xmlns="http://purl.org/rss/1.0/"><title>Comparison of two encapsulated curcumin particular systems contained in different formulations with regard to in vitro skin penetration</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00600.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Comparison of two encapsulated curcumin particular systems contained in different formulations with regard to in vitro skin penetration</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">N. Suwannateep</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. Wanichwecharungruang</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Fluhr</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Patzelt</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Lademann</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. C. Meinke</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-11T03:22:54.553269-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00600.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00600.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00600.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt600-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Curcumin is known for its anti-inflammatory, antioxidative, and anticarcinogenic properties. However, the strong lipophilic compound is not easily applicable, neither in water, nor directly in o/w formulations. So far, loading of nano or micro scaled carriers has enabled only an uptake up to 30% of curcumin.</p></div></div><div class="section" id="srt600-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Method</h3><div class="para"><p>In the present article, curcumin was successfully encapsulated into two different safe and inexpensive polymers, ethyl cellulose and methyl cellulose blended ethyl cellulose with a loading capacity of ~ 46–48%. In addition, the <em>in vitro</em> skin penetration of the two curcumin encapsulated particular systems, which were applied each in three different formulations, an o/w, w/o lotion, and water suspension, was investigated on porcine ear skin using Laser scanning microscopy.</p></div></div><div class="section" id="srt600-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>It was found that in comparison to water suspensions, o/w and w/o lotions enhanced, especially the follicular penetration of the encapsulated curcumin particles into porcine skin, whereas the w/o enhanced the penetration better than the o/w lotion. Furthermore, the application of ethyl cellulose blended with methyl cellulose improved the penetration of curcumin in all formulations.</p></div></div><div class="section" id="srt600-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>High loaded encapsulated curcumin systems, prepared from a simple and highly efficient encapsulation system can be used to transport curcumin effectively into the skin.</p></div></div>]]></content:encoded><description>BackgroundCurcumin is known for its anti-inflammatory, antioxidative, and anticarcinogenic properties. However, the strong lipophilic compound is not easily applicable, neither in water, nor directly in o/w formulations. So far, loading of nano or micro scaled carriers has enabled only an uptake up to 30% of curcumin.MethodIn the present article, curcumin was successfully encapsulated into two different safe and inexpensive polymers, ethyl cellulose and methyl cellulose blended ethyl cellulose with a loading capacity of ~ 46–48%. In addition, the in vitro skin penetration of the two curcumin encapsulated particular systems, which were applied each in three different formulations, an o/w, w/o lotion, and water suspension, was investigated on porcine ear skin using Laser scanning microscopy.ResultsIt was found that in comparison to water suspensions, o/w and w/o lotions enhanced, especially the follicular penetration of the encapsulated curcumin particles into porcine skin, whereas the w/o enhanced the penetration better than the o/w lotion. Furthermore, the application of ethyl cellulose blended with methyl cellulose improved the penetration of curcumin in all formulations.ConclusionHigh loaded encapsulated curcumin systems, prepared from a simple and highly efficient encapsulation system can be used to transport curcumin effectively into the skin.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00602.x" xmlns="http://purl.org/rss/1.0/"><title>Automatic dirt trail analysis in dermoscopy images</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00602.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Automatic dirt trail analysis in dermoscopy images</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Beibei Cheng</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. Joe Stanley</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">William V. Stoecker</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christopher T. P. Osterwise</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sherea M. Stricklin</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kristen A. Hinton</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Randy H. Moss</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Margaret Oliviero</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Harold S. Rabinovitz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-11T03:22:35.982137-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00602.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00602.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00602.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt602-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Basal cell carcinoma (BCC) is the most common cancer in the US. Dermatoscopes are devices used by physicians to facilitate the early detection of these cancers based on the identification of skin lesion structures often specific to BCCs. One new lesion structure, referred to as dirt trails, has the appearance of dark gray, brown or black dots and clods of varying sizes distributed in elongated clusters with indistinct borders, often appearing as curvilinear trails.</p></div></div><div class="section" id="srt602-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>In this research, we explore a dirt trail detection and analysis algorithm for extracting, measuring, and characterizing dirt trails based on size, distribution, and color in dermoscopic skin lesion images. These dirt trails are then used to automatically discriminate BCC from benign skin lesions.</p></div></div><div class="section" id="srt602-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>For an experimental data set of 35 BCC images with dirt trails and 79 benign lesion images, a neural network-based classifier achieved a 0.902 are under a receiver operating characteristic curve using a leave-one-out approach.</p></div></div><div class="section" id="srt602-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Results obtained from this study show that automatic detection of dirt trails in dermoscopic images of BCC is feasible. This is important because of the large number of these skin cancers seen every year and the challenge of discovering these earlier with instrumentation.</p></div></div>]]></content:encoded><description>BackgroundBasal cell carcinoma (BCC) is the most common cancer in the US. Dermatoscopes are devices used by physicians to facilitate the early detection of these cancers based on the identification of skin lesion structures often specific to BCCs. One new lesion structure, referred to as dirt trails, has the appearance of dark gray, brown or black dots and clods of varying sizes distributed in elongated clusters with indistinct borders, often appearing as curvilinear trails.MethodsIn this research, we explore a dirt trail detection and analysis algorithm for extracting, measuring, and characterizing dirt trails based on size, distribution, and color in dermoscopic skin lesion images. These dirt trails are then used to automatically discriminate BCC from benign skin lesions.ResultsFor an experimental data set of 35 BCC images with dirt trails and 79 benign lesion images, a neural network-based classifier achieved a 0.902 are under a receiver operating characteristic curve using a leave-one-out approach.ConclusionResults obtained from this study show that automatic detection of dirt trails in dermoscopic images of BCC is feasible. This is important because of the large number of these skin cancers seen every year and the challenge of discovering these earlier with instrumentation.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00609.x" xmlns="http://purl.org/rss/1.0/"><title>Gender-dependent differences in degree of facial wrinkles</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00609.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Gender-dependent differences in degree of facial wrinkles</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kazue Tsukahara</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mitsuyuki Hotta</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Osamu Osanai</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hiromitsu Kawada</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Takashi Kitahara</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yoshinori Takema</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-11T03:22:19.405588-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00609.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00609.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00609.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt609-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background/purpose</h3><div class="para"><p>This study aimed to reveal gender-dependent differences in the degree of facial wrinkles.</p></div></div><div class="section" id="srt609-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Subjects comprised 173 Japanese men and women, divided into four groups according to age. Photographs were taken from nine facial regions and used to classify the intensity of wrinkles into five grades. In addition, replicas were taken from five facial sites and used to measure surface roughness. Data were compared between men and women within each age group.</p></div></div><div class="section" id="srt609-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>In all age groups, men showed increased forehead wrinkles compared with women. In contrast, no gender-dependent differences were found in upper eyelid wrinkles. Other facial wrinkles were greater in men than in women in all except the oldest group (age, 65–75 years), in which wrinkles in women were greater than or equal to those in men.</p></div></div><div class="section" id="srt609-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Our results showed that gender-dependent differences exist in the degree of facial wrinkles. In general, men tend to have more severe wrinkles than women. This tendency disappeared or was reversed in some regions of the face and in individuals more than 60 years old.</p></div></div>]]></content:encoded><description>Background/purposeThis study aimed to reveal gender-dependent differences in the degree of facial wrinkles.MethodsSubjects comprised 173 Japanese men and women, divided into four groups according to age. Photographs were taken from nine facial regions and used to classify the intensity of wrinkles into five grades. In addition, replicas were taken from five facial sites and used to measure surface roughness. Data were compared between men and women within each age group.ResultsIn all age groups, men showed increased forehead wrinkles compared with women. In contrast, no gender-dependent differences were found in upper eyelid wrinkles. Other facial wrinkles were greater in men than in women in all except the oldest group (age, 65–75 years), in which wrinkles in women were greater than or equal to those in men.ConclusionOur results showed that gender-dependent differences exist in the degree of facial wrinkles. In general, men tend to have more severe wrinkles than women. This tendency disappeared or was reversed in some regions of the face and in individuals more than 60 years old.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00596.x" xmlns="http://purl.org/rss/1.0/"><title>Liquid-crystalline membrane permeation ability for selected nitro hair dyes</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00596.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Liquid-crystalline membrane permeation ability for selected nitro hair dyes</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Iwona Bialas</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jacek Arct</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Miroslaw Mojski</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Stanislaw Krus</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-04T01:05:32.173419-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00596.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00596.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00596.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt596-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Aim</h3><div class="para"><p>A comparison of permeation ability of selected semi-permanent hair dyes and an attempt to estimate the influence of fundamental physicochemical parameters on dyes’ epidermal penetration rate.</p></div></div><div class="section" id="srt596-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Dyes’ permeation ability through liposome membrane (as a model of stratum corneum) with side-by-side cells was assessed.</p></div></div><div class="section" id="srt596-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>It has been shown that the chosen dyes are capable of permeating the membrane. High penetration coefficients (<em>K</em>p) were obtained for a simple nitrophenylenediamines and nitroaminophenols. Their N-, O-hydroxyalkyl substitution significantly limits penetration. H-bonding capability has a major impact on the investigated dyes’ permeation ability. Substituents with H-bonding properties can significantly limit dyes’ penetration, even in the case of lipophilic structures. Special attention should be placed into compounds with strong intramolecular H-bonding properties, which improve transmembrane transport.</p></div></div><div class="section" id="srt596-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Substitution patterns have an influence on selected nitro dyes’ permeation through a model stratum corneum. Permeation is limited by dyes diffusive properties (mostly by its H-bonding properties). Hydroxyalkylation results in hindered dyes permeation: purple, violet and blue nitrophenylenediamine or nitroaminophenol derivatives are less permeable than its not substituted analogues.</p></div></div>]]></content:encoded><description>AimA comparison of permeation ability of selected semi-permanent hair dyes and an attempt to estimate the influence of fundamental physicochemical parameters on dyes’ epidermal penetration rate.MethodsDyes’ permeation ability through liposome membrane (as a model of stratum corneum) with side-by-side cells was assessed.ResultsIt has been shown that the chosen dyes are capable of permeating the membrane. High penetration coefficients (Kp) were obtained for a simple nitrophenylenediamines and nitroaminophenols. Their N-, O-hydroxyalkyl substitution significantly limits penetration. H-bonding capability has a major impact on the investigated dyes’ permeation ability. Substituents with H-bonding properties can significantly limit dyes’ penetration, even in the case of lipophilic structures. Special attention should be placed into compounds with strong intramolecular H-bonding properties, which improve transmembrane transport.ConclusionSubstitution patterns have an influence on selected nitro dyes’ permeation through a model stratum corneum. Permeation is limited by dyes diffusive properties (mostly by its H-bonding properties). Hydroxyalkylation results in hindered dyes permeation: purple, violet and blue nitrophenylenediamine or nitroaminophenol derivatives are less permeable than its not substituted analogues.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00608.x" xmlns="http://purl.org/rss/1.0/"><title>A comparative study of hair shafts in scalp psoriasis and seborrheic dermatitis using atomic force microscopy</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00608.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A comparative study of hair shafts in scalp psoriasis and seborrheic dermatitis using atomic force microscopy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kyung Sook Kim</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. K. Shin</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. J. Ahn</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. R. Haw</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hun-Kuk Park</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-01-04T00:36:28.864722-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00608.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00608.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00608.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt608-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>As the inflammatory scalp conditions share similar clinical manifestations of scaling, inflammation, and pruritus, the differential diagnosis of these lesions; especially between scalp psoriasis (SP) and seborrheic dermatitis (SD) is sometimes difficult.</p></div></div><div class="section" id="srt608-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Objectives</h3><div class="para"><p>The aim of this study was to investigate the differences on the hair surface in SP and SD for a clinical diagnosis, using atomic force microscopy (AFM).</p></div></div><div class="section" id="srt608-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>The hair shafts of 14 patients and 28 patients with SP and SD respectively, were taken from the lesional region. Hairs from healthy adults not having any hair diseases were also examined in the same way for the controls. Surface characteristics of SP and SD-affected hair shafts such as, pitting, scale thickness, and roughness, were observed on the AFM images.</p></div></div><div class="section" id="srt608-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>One hundred percentage and four percentage of the patients with SP and SD respectively had macropits on their hair shafts. In both the SP and SD-affected hairs, the scale thickness was more than 4-fold than that in the control hairs. The surface of SP-affected hairs was rougher than that of SD-affected and control hairs.</p></div></div><div class="section" id="srt608-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>The differences in hair shafts between SP and SD were investigated noninvasively using AFM. The presence of macropits could be helpful in the differentiation between SP and SD.</p></div></div>]]></content:encoded><description>BackgroundAs the inflammatory scalp conditions share similar clinical manifestations of scaling, inflammation, and pruritus, the differential diagnosis of these lesions; especially between scalp psoriasis (SP) and seborrheic dermatitis (SD) is sometimes difficult.ObjectivesThe aim of this study was to investigate the differences on the hair surface in SP and SD for a clinical diagnosis, using atomic force microscopy (AFM).MethodsThe hair shafts of 14 patients and 28 patients with SP and SD respectively, were taken from the lesional region. Hairs from healthy adults not having any hair diseases were also examined in the same way for the controls. Surface characteristics of SP and SD-affected hair shafts such as, pitting, scale thickness, and roughness, were observed on the AFM images.ResultsOne hundred percentage and four percentage of the patients with SP and SD respectively had macropits on their hair shafts. In both the SP and SD-affected hairs, the scale thickness was more than 4-fold than that in the control hairs. The surface of SP-affected hairs was rougher than that of SD-affected and control hairs.ConclusionThe differences in hair shafts between SP and SD were investigated noninvasively using AFM. The presence of macropits could be helpful in the differentiation between SP and SD.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00605.x" xmlns="http://purl.org/rss/1.0/"><title>Sebum, acne, skin elasticity, and gender difference – which is the major influencing factor for facial pores?</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00605.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Sebum, acne, skin elasticity, and gender difference – which is the major influencing factor for facial pores?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">BY Kim</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">JW Choi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">KC Park</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">SW Youn</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-28T02:48:36.60104-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00605.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00605.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00605.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt605-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Enlarged facial pores have been esthetic problems and have become a matter of cosmetic concern. Several factors are supposed to be related to the enlargement of facial pores, although scientific evaluations were not performed yet.</p></div></div><div class="section" id="srt605-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Objective</h3><div class="para"><p>To assess the correlation between facial pores and possible relating factors such as age, gender, sebum secretion, skin elasticity, and the presence of acne, using objective bioengineering instruments.</p></div></div><div class="section" id="srt605-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Sixty volunteers, 30 males and 30 females, participated in this study. Various parameters of facial pores were assessed using the Robo Skin Analyzer<sup>®</sup>. The facial sebum secretion and skin elasticity were measured using the Sebumeter<sup>®</sup> and the Cutometer<sup>®</sup>, respectively. These data were compared and correlated to examine the possible relationship between facial pores and age, sebum secretion and skin elasticity, according to gender and the presence of acne.</p></div></div><div class="section" id="srt605-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Male gender and the existence of acne were correlated with higher number of facial pores. Sebum secretion levels showed positive correlation with facial pores. The R7 parameter of skin elasticity was negatively correlated with facial pores, suggesting increased facial pores with decreased skin elasticity. However, the age and the severity of acne did not show a definite relationship with facial pores.</p></div></div><div class="section" id="srt605-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Male, increased sebum and decreased skin elasticity were mostly correlated with facial pore development. Further studies on population with various demographic profiles and more severe acne may be helpful to elucidate the potential effect of aging and acne severity on facial pores.</p></div></div>]]></content:encoded><description>BackgroundEnlarged facial pores have been esthetic problems and have become a matter of cosmetic concern. Several factors are supposed to be related to the enlargement of facial pores, although scientific evaluations were not performed yet.ObjectiveTo assess the correlation between facial pores and possible relating factors such as age, gender, sebum secretion, skin elasticity, and the presence of acne, using objective bioengineering instruments.MethodsSixty volunteers, 30 males and 30 females, participated in this study. Various parameters of facial pores were assessed using the Robo Skin Analyzer®. The facial sebum secretion and skin elasticity were measured using the Sebumeter® and the Cutometer®, respectively. These data were compared and correlated to examine the possible relationship between facial pores and age, sebum secretion and skin elasticity, according to gender and the presence of acne.ResultsMale gender and the existence of acne were correlated with higher number of facial pores. Sebum secretion levels showed positive correlation with facial pores. The R7 parameter of skin elasticity was negatively correlated with facial pores, suggesting increased facial pores with decreased skin elasticity. However, the age and the severity of acne did not show a definite relationship with facial pores.ConclusionMale, increased sebum and decreased skin elasticity were mostly correlated with facial pore development. Further studies on population with various demographic profiles and more severe acne may be helpful to elucidate the potential effect of aging and acne severity on facial pores.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00603.x" xmlns="http://purl.org/rss/1.0/"><title>A Feature-Preserving Hair Removal Algorithm for Dermoscopy Images</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00603.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A Feature-Preserving Hair Removal Algorithm for Dermoscopy Images</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Qaisar Abbas</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Irene Fondón Garcia</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Emre Celebi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Waqar Ahmad</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-28T02:48:33.393846-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00603.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00603.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00603.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt603-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background/purpose</h3><div class="para"><p>Accurate segmentation and repair of hair-occluded information from dermoscopy images are challenging tasks for computer-aided detection (CAD) of melanoma. Currently, many hair-restoration algorithms have been developed, but most of these fail to identify hairs accurately and their removal technique is slow and disturbs the lesion's pattern.</p></div></div><div class="section" id="srt603-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>In this article, a novel hair-restoration algorithm is presented, which has a capability to preserve the skin lesion features such as color and texture and able to segment both dark and light hairs. Our algorithm is based on three major steps: the rough hairs are segmented using a matched filtering with first derivative of gaussian (MF-FDOG) with thresholding that generate strong responses for both dark and light hairs, refinement of hairs by morphological edge-based techniques, which are repaired through a fast marching inpainting method. Diagnostic accuracy (DA) and texture-quality measure (TQM) metrics are utilized based on dermatologist-drawn manual hair masks that were used as a ground truth to evaluate the performance of the system.</p></div></div><div class="section" id="srt603-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>The hair-restoration algorithm is tested on 100 dermoscopy images. The comparisons have been done among (i) linear interpolation, inpainting by (ii) non-linear partial differential equation (PDE), and (iii) exemplar-based repairing techniques. Among different hair detection and removal techniques, our proposed algorithm obtained the highest value of DA: 93.3% and TQM: 90%.</p></div></div><div class="section" id="srt603-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>The experimental results indicate that the proposed algorithm is highly accurate, robust and able to restore hair pixels without damaging the lesion texture. This method is fully automatic and can be easily integrated into a CAD system.</p></div></div>]]></content:encoded><description>Background/purposeAccurate segmentation and repair of hair-occluded information from dermoscopy images are challenging tasks for computer-aided detection (CAD) of melanoma. Currently, many hair-restoration algorithms have been developed, but most of these fail to identify hairs accurately and their removal technique is slow and disturbs the lesion's pattern.MethodsIn this article, a novel hair-restoration algorithm is presented, which has a capability to preserve the skin lesion features such as color and texture and able to segment both dark and light hairs. Our algorithm is based on three major steps: the rough hairs are segmented using a matched filtering with first derivative of gaussian (MF-FDOG) with thresholding that generate strong responses for both dark and light hairs, refinement of hairs by morphological edge-based techniques, which are repaired through a fast marching inpainting method. Diagnostic accuracy (DA) and texture-quality measure (TQM) metrics are utilized based on dermatologist-drawn manual hair masks that were used as a ground truth to evaluate the performance of the system.ResultsThe hair-restoration algorithm is tested on 100 dermoscopy images. The comparisons have been done among (i) linear interpolation, inpainting by (ii) non-linear partial differential equation (PDE), and (iii) exemplar-based repairing techniques. Among different hair detection and removal techniques, our proposed algorithm obtained the highest value of DA: 93.3% and TQM: 90%.ConclusionThe experimental results indicate that the proposed algorithm is highly accurate, robust and able to restore hair pixels without damaging the lesion texture. This method is fully automatic and can be easily integrated into a CAD system.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00601.x" xmlns="http://purl.org/rss/1.0/"><title>Emerging applications of nanomedicine in dermatology</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00601.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Emerging applications of nanomedicine in dermatology</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rosita Saraceno</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Andrea Chiricozzi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Massimo Gabellini</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sergio Chimenti</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-18T21:59:28.149847-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00601.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00601.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00601.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Review Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt601-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Nanotechnology is a new branch of engineering consisting of the usage of nanoscale particles (100 nm and smaller). Nanomedicine is the application of nanoscale technologies for diagnostic and therapeutic purposes in medicine. Nanodermatology, nanotechnology applied to dermatology, represents one of the most advanced field for which an increasing interest, both economic and scientific, is rising.</p></div><div class="para"><p> The skin is the first point of contact for a whole host of nanomaterials, ranging from topical preparations, articles of clothing and household products, to sporting goods and industrial manufactured goods.</p></div><div class="para"><p> Applications of nanomedicine in dermatology include new direction in medical diagnosis, monitoring and treatment. Gold nanoparticle, quantum dots and magnetic nanoparticles are used in non-invasive nanoimaging of high-resolution dermoscopy, microscopy, nanopunch, and spectroscopy, offering advanced diagnostic and therapeutic modalities.</p></div><div class="para"><p> Nanotherapeutics has been considered in immunotherapy, genetherapy, and drug therapy. In drug therapy, because of size reduction or encapsulation of drug particles, the therapeutic potential of water insoluble and unstable drugs improve, and also facilitate the delivery of small molecules across blood, skin, nails, and pilosebaceous unit.</p></div></div><div class="section" id="srt601-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Aims</h3><div class="para"><p>To review therapeutic applications and benefits of nanomedicine in esthetic dermatology, treatment of malignancies, and inflammatory skin diseases.</p></div></div>]]></content:encoded><description>BackgroundNanotechnology is a new branch of engineering consisting of the usage of nanoscale particles (100 nm and smaller). Nanomedicine is the application of nanoscale technologies for diagnostic and therapeutic purposes in medicine. Nanodermatology, nanotechnology applied to dermatology, represents one of the most advanced field for which an increasing interest, both economic and scientific, is rising. The skin is the first point of contact for a whole host of nanomaterials, ranging from topical preparations, articles of clothing and household products, to sporting goods and industrial manufactured goods. Applications of nanomedicine in dermatology include new direction in medical diagnosis, monitoring and treatment. Gold nanoparticle, quantum dots and magnetic nanoparticles are used in non-invasive nanoimaging of high-resolution dermoscopy, microscopy, nanopunch, and spectroscopy, offering advanced diagnostic and therapeutic modalities. Nanotherapeutics has been considered in immunotherapy, genetherapy, and drug therapy. In drug therapy, because of size reduction or encapsulation of drug particles, the therapeutic potential of water insoluble and unstable drugs improve, and also facilitate the delivery of small molecules across blood, skin, nails, and pilosebaceous unit.AimsTo review therapeutic applications and benefits of nanomedicine in esthetic dermatology, treatment of malignancies, and inflammatory skin diseases.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00607.x" xmlns="http://purl.org/rss/1.0/"><title>A novel method to investigate the relationship between facial movements and wrinkle formation using particle image velocimetry</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00607.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A novel method to investigate the relationship between facial movements and wrinkle formation using particle image velocimetry</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Tsutomu Fujimura</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mitsuyuki Hotta</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-18T21:57:24.4742-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00607.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00607.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00607.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt607-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>The possible relationship between the direction of wrinkles and the movement of facial skin has not previously been reported. Therefore, we characterized that relationship using particle image velocimetry (PIV) analysis.</p></div></div><div class="section" id="srt607-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Method</h3><div class="para"><p>Twenty-one healthy Japanese women aged in their 20s (<em>n</em> = 7) or 50s (<em>n</em> = 14) were recruited for this study. Moving images of facial skin motions (closing the eyes tightly, raising the eyebrows) were captured using a single infrared camera under infrared ray irradiation of the skin. PIV analysis was then carried out using Flow-Vec32<sup>™</sup> software to determine the velocity and the direction of skin surface movements.</p></div></div><div class="section" id="srt607-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>All skin movements caused by those motions were finished within 0.20 s. During the motion of closing the eyes, skin at the eye periphery did not move in a superior–inferior direction, but did move toward the center of the eye (pupilla) with complex flows. There was no significant difference between either age group of subjects. During the motion of raising the eyebrows, the forehead skin moved upwards (direction to parietal) with relatively uniform flows. The velocity of movement at the top was lower than at the bottom, and that difference is likely to cause a deformation on the skin surface. A significant difference between the two age groups in the velocity was observed.</p></div></div><div class="section" id="srt607-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>The results show that the deformation of older skin on the forehead is greater than that in younger skin. The PIV analysis method is a useful tool to investigate some aspects of the relationship between facial skin movements and wrinkle formation.</p></div></div>]]></content:encoded><description>BackgroundThe possible relationship between the direction of wrinkles and the movement of facial skin has not previously been reported. Therefore, we characterized that relationship using particle image velocimetry (PIV) analysis.MethodTwenty-one healthy Japanese women aged in their 20s (n = 7) or 50s (n = 14) were recruited for this study. Moving images of facial skin motions (closing the eyes tightly, raising the eyebrows) were captured using a single infrared camera under infrared ray irradiation of the skin. PIV analysis was then carried out using Flow-Vec32™ software to determine the velocity and the direction of skin surface movements.ResultsAll skin movements caused by those motions were finished within 0.20 s. During the motion of closing the eyes, skin at the eye periphery did not move in a superior–inferior direction, but did move toward the center of the eye (pupilla) with complex flows. There was no significant difference between either age group of subjects. During the motion of raising the eyebrows, the forehead skin moved upwards (direction to parietal) with relatively uniform flows. The velocity of movement at the top was lower than at the bottom, and that difference is likely to cause a deformation on the skin surface. A significant difference between the two age groups in the velocity was observed.ConclusionThe results show that the deformation of older skin on the forehead is greater than that in younger skin. The PIV analysis method is a useful tool to investigate some aspects of the relationship between facial skin movements and wrinkle formation.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00597.x" xmlns="http://purl.org/rss/1.0/"><title>NIR and skin impedance spectroscopic measurements for studying the effect of coffee and alcohol on skin, and dysplastic naevi</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00597.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">NIR and skin impedance spectroscopic measurements for studying the effect of coffee and alcohol on skin, and dysplastic naevi</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ida Bodén</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Josefina Nyström</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Paul Geladi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Peter Naredi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Britta Lindholm-Sethson</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-18T21:41:40.815847-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00597.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00597.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00597.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt597-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background/purpose</h3><div class="para"><p>Near infrared and impedance spectroscopy can be used for clinical skin measurements and need to be evaluated for possible confounding factors; (i) are skin conditions of the patient and the subsequent skin measurements influenced by alcohol and/or coffee consumption and (ii) are measurements of dysplastic naevi (DN) reproducible over time and significantly different compared to reference skin.</p></div></div><div class="section" id="srt597-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Near infrared and skin impedance spectroscopic data were analysed multivariately. In the first study, the skin characteristics of 15 healthy individuals were examined related to body location, gender, individual differences, and consumption of coffee or alcohol. The second study included five patients diagnosed with dysplastic naevi syndrome. Measurements were taken on DN and reference skin over time.</p></div></div><div class="section" id="srt597-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>In the first study, body location and gender had a major influence on measurement scores. Inter-individual skin characteristics and coffee or alcohol effects on skin characteristics were of minor importance. In the second study, it was shown that DN can be differentiated from reference skin and the measurements are stable over time.</p></div></div><div class="section" id="srt597-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusions</h3><div class="para"><p>Moderate consumption of alcohol and coffee did not influence the results of the measurements. It is possible to follow, stable or changed, characteristics of DN over time.</p></div></div>]]></content:encoded><description>Background/purposeNear infrared and impedance spectroscopy can be used for clinical skin measurements and need to be evaluated for possible confounding factors; (i) are skin conditions of the patient and the subsequent skin measurements influenced by alcohol and/or coffee consumption and (ii) are measurements of dysplastic naevi (DN) reproducible over time and significantly different compared to reference skin.MethodsNear infrared and skin impedance spectroscopic data were analysed multivariately. In the first study, the skin characteristics of 15 healthy individuals were examined related to body location, gender, individual differences, and consumption of coffee or alcohol. The second study included five patients diagnosed with dysplastic naevi syndrome. Measurements were taken on DN and reference skin over time.ResultsIn the first study, body location and gender had a major influence on measurement scores. Inter-individual skin characteristics and coffee or alcohol effects on skin characteristics were of minor importance. In the second study, it was shown that DN can be differentiated from reference skin and the measurements are stable over time.ConclusionsModerate consumption of alcohol and coffee did not influence the results of the measurements. It is possible to follow, stable or changed, characteristics of DN over time.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00577.x" xmlns="http://purl.org/rss/1.0/"><title>Visual and confocal microscopic interpretation of patch tests to benzethonium chloride and benzalkonium chloride</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00577.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Visual and confocal microscopic interpretation of patch tests to benzethonium chloride and benzalkonium chloride</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bohaty Benjamin</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Fricker Chris</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">González Salvador</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gill Melissa</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nedorost Susan</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-05T21:41:37.461763-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00577.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00577.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00577.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt577-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Quaternary ammonium compounds (Quats), such as benzalkonium chloride (BAC) and benzethonium chloride (BEC), are widely used as antibacterial active ingredients and preservatives in personal care products, disinfectants, and ophthalmic preparations. BAC is known to be a marginal irritant when patch tested at 0.15% aq. Data on BEC are limited.</p></div></div><div class="section" id="srt577-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Objective</h3><div class="para"><p>To differentiate irritant from allergic patch test reactions to quaternary ammonium compounds.</p></div></div><div class="section" id="srt577-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Eight subjects who were considered likely to react based on history of rash after exposure to disinfectants or a history of prior positive patch test to BAC were recruited, as well as two patients undergoing routine patch testing. BAC (0.15% aq), BAC (0.15% pet), BEC (0.05% aq), BEC (0.15% pet), BEC (0.15% aq), BEC (0.5% aq), sodium lauryl sulfate (2.0%), and deionized water were applied under Finn chambers for 48 h. Four days and 7 days after application, the sites were examined visually and then by <em>in vivo</em> reflectance confocal microscopy (RCM) which was interpreted by blinded experts.</p></div></div><div class="section" id="srt577-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Two patients with definite allergic reactions according to visual patch test reads and RCM were clinically relevant. Cross-reaction between BEC and BAC was demonstrated in one patient. RCM imaging correlated well with clinical scoring and interpretation of patch test reactions in terms of irritancy vs. allergy for BEC and BAC.</p></div></div><div class="section" id="srt577-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Relevant allergic reactions to quats occur in humans. Possible cross-reaction was noted to occur between BAC and BEC. RCM appears to be a useful tool in distinguishing between irritancy and sensitization during patch testing to BAC and BEC. Further study of prevalence and best test concentration and vehicle is needed.</p></div></div>]]></content:encoded><description>BackgroundQuaternary ammonium compounds (Quats), such as benzalkonium chloride (BAC) and benzethonium chloride (BEC), are widely used as antibacterial active ingredients and preservatives in personal care products, disinfectants, and ophthalmic preparations. BAC is known to be a marginal irritant when patch tested at 0.15% aq. Data on BEC are limited.ObjectiveTo differentiate irritant from allergic patch test reactions to quaternary ammonium compounds.MethodsEight subjects who were considered likely to react based on history of rash after exposure to disinfectants or a history of prior positive patch test to BAC were recruited, as well as two patients undergoing routine patch testing. BAC (0.15% aq), BAC (0.15% pet), BEC (0.05% aq), BEC (0.15% pet), BEC (0.15% aq), BEC (0.5% aq), sodium lauryl sulfate (2.0%), and deionized water were applied under Finn chambers for 48 h. Four days and 7 days after application, the sites were examined visually and then by in vivo reflectance confocal microscopy (RCM) which was interpreted by blinded experts.ResultsTwo patients with definite allergic reactions according to visual patch test reads and RCM were clinically relevant. Cross-reaction between BEC and BAC was demonstrated in one patient. RCM imaging correlated well with clinical scoring and interpretation of patch test reactions in terms of irritancy vs. allergy for BEC and BAC.ConclusionRelevant allergic reactions to quats occur in humans. Possible cross-reaction was noted to occur between BAC and BEC. RCM appears to be a useful tool in distinguishing between irritancy and sensitization during patch testing to BAC and BEC. Further study of prevalence and best test concentration and vehicle is needed.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00582.x" xmlns="http://purl.org/rss/1.0/"><title>Gender differences in facial skin dielectric constant measured at 300 MHz</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00582.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Gender differences in facial skin dielectric constant measured at 300 MHz</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Harvey N. Mayrovitz</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Maria Bernal</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sophia Carson</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-05T21:13:49.149251-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00582.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00582.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00582.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt582-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background/purpose</h3><div class="para"><p>Skin tissue dielectric constant (TDC) measurements at 300 MHz provide non-invasive data on free and bound tissue water. TDC-data is available for some body sites, but most is for female forearm. Contrastingly, there are no data on face-skin or comparative data between genders. Our goals were to obtain facial-TDC reference values and determine if TDC-values differ between genders.</p></div></div><div class="section" id="srt582-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>TDC was measured at forehead, cheek, and forearm in 60 young adults (30 men) to a 1.5-mm depth. Measured TDC-values were compared with TDC-values calculated using skin-thickness data.</p></div></div><div class="section" id="srt582-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Measured TDC-values ranged from 39.6 ± 2.9 at male-forehead to 28.2 ± 2.4 at female forearm and were significantly different (<em>P</em> &lt; 0.001) among each site in the order forehead &gt; cheek &gt;forearm. Male TDC-values were greater than female TDC-values (<em>P</em> &lt; 0.01) with differences from 5.6% at forehead to 11.3% at forearm. Calculated TDC-values incorporating site and gender skin-thickness differences yielded TDC-values at the most 3% different from measured values.</p></div></div><div class="section" id="srt582-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Gender differences should be considered in clinical studies in which men and women are included in a common study population with respect to experimental design and data interpretation. This is especially true if absolute TDC-values are of interest rather than changes in TDC-values on the same subject subsequent secondary to an intervention.</p></div></div>]]></content:encoded><description>Background/purposeSkin tissue dielectric constant (TDC) measurements at 300 MHz provide non-invasive data on free and bound tissue water. TDC-data is available for some body sites, but most is for female forearm. Contrastingly, there are no data on face-skin or comparative data between genders. Our goals were to obtain facial-TDC reference values and determine if TDC-values differ between genders.MethodsTDC was measured at forehead, cheek, and forearm in 60 young adults (30 men) to a 1.5-mm depth. Measured TDC-values were compared with TDC-values calculated using skin-thickness data.ResultsMeasured TDC-values ranged from 39.6 ± 2.9 at male-forehead to 28.2 ± 2.4 at female forearm and were significantly different (P &lt; 0.001) among each site in the order forehead &gt; cheek &gt;forearm. Male TDC-values were greater than female TDC-values (P &lt; 0.01) with differences from 5.6% at forehead to 11.3% at forearm. Calculated TDC-values incorporating site and gender skin-thickness differences yielded TDC-values at the most 3% different from measured values.ConclusionGender differences should be considered in clinical studies in which men and women are included in a common study population with respect to experimental design and data interpretation. This is especially true if absolute TDC-values are of interest rather than changes in TDC-values on the same subject subsequent secondary to an intervention.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00584.x" xmlns="http://purl.org/rss/1.0/"><title>Automatic telangiectasia analysis in dermoscopy images using adaptive critic design</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00584.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Automatic telangiectasia analysis in dermoscopy images using adaptive critic design</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">B. Cheng</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. J. Stanley</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">W. V. Stoecker</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. Hinton</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-12-05T07:11:22.032216-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00584.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00584.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00584.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt584-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Telangiectasia, tiny skin vessels, are important dermoscopy structures used to discriminate basal cell carcinoma (BCC) from benign skin lesions. This research builds off of previously developed image analysis techniques to identify vessels automatically to discriminate benign lesions from BCCs.</p></div></div><div class="section" id="srt584-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>A biologically inspired reinforcement learning approach is investigated in an adaptive critic design framework to apply action-dependent heuristic dynamic programming (ADHDP) for discrimination based on computed features using different skin lesion contrast variations to promote the discrimination process. Lesion discrimination results for ADHDP are compared with multilayer perception backpropagation artificial neural networks.</p></div></div><div class="section" id="srt584-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>This study uses a data set of 498 dermoscopy skin lesion images of 263 BCCs and 226 competitive benign images as the input sets. This data set is extended from previous research [Cheng et al., <em>Skin Research and Technology</em>, 2011, 17: 278]. Experimental results yielded a diagnostic accuracy as high as 84.6% using the ADHDP approach, providing an 8.03% improvement over a standard multilayer perception method.</p></div></div><div class="section" id="srt584-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>We have chosen BCC detection rather than vessel detection as the endpoint. Although vessel detection is inherently easier, BCC detection has potential direct clinical applications. Small BCCs are detectable early by dermoscopy and potentially detectable by the automated methods described in this research.</p></div></div>]]></content:encoded><description>BackgroundTelangiectasia, tiny skin vessels, are important dermoscopy structures used to discriminate basal cell carcinoma (BCC) from benign skin lesions. This research builds off of previously developed image analysis techniques to identify vessels automatically to discriminate benign lesions from BCCs.MethodsA biologically inspired reinforcement learning approach is investigated in an adaptive critic design framework to apply action-dependent heuristic dynamic programming (ADHDP) for discrimination based on computed features using different skin lesion contrast variations to promote the discrimination process. Lesion discrimination results for ADHDP are compared with multilayer perception backpropagation artificial neural networks.ResultsThis study uses a data set of 498 dermoscopy skin lesion images of 263 BCCs and 226 competitive benign images as the input sets. This data set is extended from previous research [Cheng et al., Skin Research and Technology, 2011, 17: 278]. Experimental results yielded a diagnostic accuracy as high as 84.6% using the ADHDP approach, providing an 8.03% improvement over a standard multilayer perception method.ConclusionWe have chosen BCC detection rather than vessel detection as the endpoint. Although vessel detection is inherently easier, BCC detection has potential direct clinical applications. Small BCCs are detectable early by dermoscopy and potentially detectable by the automated methods described in this research.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00579.x" xmlns="http://purl.org/rss/1.0/"><title>How long does protection last? – In vivo fluorescence confocal laser scanning imaging for the evaluation of the kinetics of a topically applied lotion in an everyday setting</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00579.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">How long does protection last? – In vivo fluorescence confocal laser scanning imaging for the evaluation of the kinetics of a topically applied lotion in an everyday setting</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">E. Sattler</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. Kästle</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Arens-Corell</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Welzel</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-24T21:59:26.53688-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00579.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00579.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00579.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt579-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Confocal laser scanning microscopic imaging is well established as a helpful diagnostic tool in dermatology. With a new generation of multi-wave laser confocal microscopes now, in addition to the reflection mode, examinations with fluorescent agents are possible <em>in kursiv</em> and <em>ex vivo</em>. Gathering details on the physical, chemical and kinetic features of different fluorophores in different vehicles in healthy skin <em>in vivo</em> will be of interest for therapeutic as well as cosmetic dermatology.</p></div></div><div class="section" id="srt579-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Objectives</h3><div class="para"><p>Objective of this study was to determine the kinetics of the protective function of a topically applied, fluorescent-containing lotion in a 24 h everyday setting in healthy volunteers using fluorescence confocal laser scanning microscopy imaging.</p></div></div><div class="section" id="srt579-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Material and methods</h3><div class="para"><p>Fifteen volunteers received a standardized application of a sodium fluoresceine containing lotion. At several time points of a 24 h interval confocal laser imaging in the multi-wave mode was performed. Fluorescence was measured by a semiquantitative score and by one based on the intensity of light.</p></div></div><div class="section" id="srt579-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>CLSM images in the depths of the stratum corneum and of the upper epidermis of all 15 panelists showed a detectable fluorescence after 30 min and 4 h and after 24 h, a partial fluorescence was still visible in 10 of 15 persons. Similar results were achieved using a semiquantitative score and by measuring the intensity of light.</p></div></div><div class="section" id="srt579-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Sodium fluoresceine as a safe and efficient fluorophore for <em>in vivo</em> fluorescence CLSM was able to visualize the kinetics of a topically applied protective lotion and was able to be detected for up to 4 h in all panelists and even up to 24 h in two-thirds of the healthy volunteers showing the long duration of the fluorescence on the skin surface, even in an everyday setting.</p></div></div>]]></content:encoded><description>BackgroundConfocal laser scanning microscopic imaging is well established as a helpful diagnostic tool in dermatology. With a new generation of multi-wave laser confocal microscopes now, in addition to the reflection mode, examinations with fluorescent agents are possible in kursiv and ex vivo. Gathering details on the physical, chemical and kinetic features of different fluorophores in different vehicles in healthy skin in vivo will be of interest for therapeutic as well as cosmetic dermatology.ObjectivesObjective of this study was to determine the kinetics of the protective function of a topically applied, fluorescent-containing lotion in a 24 h everyday setting in healthy volunteers using fluorescence confocal laser scanning microscopy imaging.Material and methodsFifteen volunteers received a standardized application of a sodium fluoresceine containing lotion. At several time points of a 24 h interval confocal laser imaging in the multi-wave mode was performed. Fluorescence was measured by a semiquantitative score and by one based on the intensity of light.ResultsCLSM images in the depths of the stratum corneum and of the upper epidermis of all 15 panelists showed a detectable fluorescence after 30 min and 4 h and after 24 h, a partial fluorescence was still visible in 10 of 15 persons. Similar results were achieved using a semiquantitative score and by measuring the intensity of light.ConclusionSodium fluoresceine as a safe and efficient fluorophore for in vivo fluorescence CLSM was able to visualize the kinetics of a topically applied protective lotion and was able to be detected for up to 4 h in all panelists and even up to 24 h in two-thirds of the healthy volunteers showing the long duration of the fluorescence on the skin surface, even in an everyday setting.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00587.x" xmlns="http://purl.org/rss/1.0/"><title>7-Tesla MR imaging of non-melanoma skin cancer samples: correlation with histopathology</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00587.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">7-Tesla MR imaging of non-melanoma skin cancer samples: correlation with histopathology</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sébastien Aubry</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Olga Leclerc</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Luc Tremblay</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Edmond Rizcallah</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Frédéric Croteau</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Charles Orfali</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Martin Lepage</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-24T21:50:46.667222-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00587.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00587.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00587.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt587-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Purpose</h3><div class="para"><p>The aims of this study were to compare <em>in vitro</em> magnetic resonance imaging (MRI) characteristics of keratinocytic skin cancer assessed by a 7-tesla (T) MRI with histopathology, and to describe MRI features of skin tumors.</p></div></div><div class="section" id="srt587-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>This prospective study included 30 skin tumors treated by surgery. MR images of skin samples were acquired on a 7-T MR scanner using a fast spin-echo <em>T</em><sub>2</sub>-weighted and an isotropic 3D gradient-echo <em>T</em><sub>1</sub>-weighted sequence. Length, width, Breslow index and margins of the lesions were measured. The presence or absence of the following was noted: healthy margins, ulceration of the dermis, <em>in situ</em> lesions, superficial and deep dermis involvement, subcutaneous involvement, superficial and intratumoral keratin. MR results were compared to histopathology.</p></div></div><div class="section" id="srt587-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Interclass correlation coefficient (ICC) was very good for the evaluation of the width (ICC = 0.86) and Breslow index (ICC = 0.87). The ICC was good for the evaluation of the margins (ICC = 0.70) but for length, ICC was lower (ICC = 0.67). Mean bias between MRI and histopathology was inferior to 1 mm for width, Breslow index and margin.</p></div></div><div class="section" id="srt587-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p><em>In vitro</em> 7-T MRI of keratinocytic skin cancer allows delineation of lesions with good correlation with histopathology. After <em>in vivo</em> confirmation it could have a diagnostic role regarding the delineation of surgical margins but its actual limitations prevent its practical adoption at this time.</p></div></div>]]></content:encoded><description>PurposeThe aims of this study were to compare in vitro magnetic resonance imaging (MRI) characteristics of keratinocytic skin cancer assessed by a 7-tesla (T) MRI with histopathology, and to describe MRI features of skin tumors.MethodsThis prospective study included 30 skin tumors treated by surgery. MR images of skin samples were acquired on a 7-T MR scanner using a fast spin-echo T2-weighted and an isotropic 3D gradient-echo T1-weighted sequence. Length, width, Breslow index and margins of the lesions were measured. The presence or absence of the following was noted: healthy margins, ulceration of the dermis, in situ lesions, superficial and deep dermis involvement, subcutaneous involvement, superficial and intratumoral keratin. MR results were compared to histopathology.ResultsInterclass correlation coefficient (ICC) was very good for the evaluation of the width (ICC = 0.86) and Breslow index (ICC = 0.87). The ICC was good for the evaluation of the margins (ICC = 0.70) but for length, ICC was lower (ICC = 0.67). Mean bias between MRI and histopathology was inferior to 1 mm for width, Breslow index and margin.ConclusionIn vitro 7-T MRI of keratinocytic skin cancer allows delineation of lesions with good correlation with histopathology. After in vivo confirmation it could have a diagnostic role regarding the delineation of surgical margins but its actual limitations prevent its practical adoption at this time.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00585.x" xmlns="http://purl.org/rss/1.0/"><title>Fluorescent fibre-optic confocal imaging of lesional and non-lesional psoriatic skin compared with normal skin in vivo</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00585.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Fluorescent fibre-optic confocal imaging of lesional and non-lesional psoriatic skin compared with normal skin in vivo</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christian Suihko</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jørgen Serup</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-24T01:08:23.817123-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00585.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00585.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00585.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt585-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background/aims</h3><div class="para"><p>Fibre-optic confocal imaging (FOCI) allows non-invasive visualization of live skin <em>in vivo</em>. A contrast agent, a fluorophore, is injected in the dermis. FOCI images are optical sections from a horizontal (en face) view. The aim was to study epidermis and the cellular structure of keratinocytes of psoriatic plaques and adjacent non-lesional with healthy skin as a reference.</p></div></div><div class="section" id="srt585-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Twelve patients with stable plaque psoriasis were studied and compared with a control group of eight healthy individuals. Fluorescein sodium was used as fluorophore. A hand held fibre-optic laser scanner (Stratum<sup>®</sup>; Optiscan Pty., Melbourne, Australia) was used. The study included morphometric analyses.</p></div></div><div class="section" id="srt585-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>The confocal <em>in vivo</em> images demonstrated characteristic features of epidermis and keratinocytes in lesional and non-lesional skin vs. healthy skin. Morphometry based on FOCI demonstrated an approximately 30% increased width of keratinocytes of psoriatic skin vs. healthy control, and the number of keratinocytes per viewing field was reduced. FOCI allowed non-invasive visualization of cell nuclei and <em>parakeratosis</em> of psoriatic epidermis. The horizontal width of dermal papillae of psoriatic skin was increased by approximately 50% as compared with healthy skin, and the flow of erythrocytes in the papillar vessels could be observed in real-time.</p></div></div><div class="section" id="srt585-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>FOCI can directly visualize essential epidermal structures of plaque psoriasis <em>in vivo,</em> in real-time and with cellular resolution without the need of taking biopsies and thus without disturbing the natural state of the skin. FOCI is a versatile future tool for non-invasive microscopic diagnosis and therapy follow-up of psoriasis.</p></div></div>]]></content:encoded><description>Background/aimsFibre-optic confocal imaging (FOCI) allows non-invasive visualization of live skin in vivo. A contrast agent, a fluorophore, is injected in the dermis. FOCI images are optical sections from a horizontal (en face) view. The aim was to study epidermis and the cellular structure of keratinocytes of psoriatic plaques and adjacent non-lesional with healthy skin as a reference.MethodsTwelve patients with stable plaque psoriasis were studied and compared with a control group of eight healthy individuals. Fluorescein sodium was used as fluorophore. A hand held fibre-optic laser scanner (Stratum®; Optiscan Pty., Melbourne, Australia) was used. The study included morphometric analyses.ResultsThe confocal in vivo images demonstrated characteristic features of epidermis and keratinocytes in lesional and non-lesional skin vs. healthy skin. Morphometry based on FOCI demonstrated an approximately 30% increased width of keratinocytes of psoriatic skin vs. healthy control, and the number of keratinocytes per viewing field was reduced. FOCI allowed non-invasive visualization of cell nuclei and parakeratosis of psoriatic epidermis. The horizontal width of dermal papillae of psoriatic skin was increased by approximately 50% as compared with healthy skin, and the flow of erythrocytes in the papillar vessels could be observed in real-time.ConclusionFOCI can directly visualize essential epidermal structures of plaque psoriasis in vivo, in real-time and with cellular resolution without the need of taking biopsies and thus without disturbing the natural state of the skin. FOCI is a versatile future tool for non-invasive microscopic diagnosis and therapy follow-up of psoriasis.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00591.x" xmlns="http://purl.org/rss/1.0/"><title>Noninvasive estimation of chronological and photoinduced skin damage using Raman spectroscopy and principal component analysis</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00591.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Noninvasive estimation of chronological and photoinduced skin damage using Raman spectroscopy and principal component analysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Francisco J. González</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Claudio Castillo-Martínez</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marcela Martínez-Escanamé</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Miguel G. Ramírez-Elías</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Francisco I. Gaitan-Gaona</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Cuauhtémoc Oros-Ovalle</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Benjamín Moncada</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-22T02:40:53.665674-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00591.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00591.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00591.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt591-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Skin aging can be attributed to endogenous and exogenous factors which modify the hydration and protein structure of the skin which can be measured using Raman spectroscopy.</p></div></div><div class="section" id="srt591-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Method</h3><div class="para"><p>This study included 21 healthy adult volunteers, aged 32–81 years, Raman spectra were obtained from sun-protected and sun-exposed skin, also three millimeter punch biopsies of sun-exposed skin were collected and analyzed. The Raman spectra were analyzed using principal component analysis and the results were correlated with clinical and histological findings.</p></div></div><div class="section" id="srt591-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>The principal component analysis of the Raman spectra shows that the first principal component (PC1) obtained from the sun-protected skin is related to the age of the subject, which can be taken as a measure of chronological aging, the second (PC2) and fourth (PC4) principal components obtained from Raman spectra of sun-exposed skin are related to the amount of solar elastosis and collagen, respectively.</p></div></div><div class="section" id="srt591-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>In this work a relationship was found between histological properties of photoaged skin and noninvasive measurements based on Raman and principal components analysis (PCA). These relationships can be used to assess noninvasively the photoinduced damage and chronological characteristics of skin.</p></div></div>]]></content:encoded><description>BackgroundSkin aging can be attributed to endogenous and exogenous factors which modify the hydration and protein structure of the skin which can be measured using Raman spectroscopy.MethodThis study included 21 healthy adult volunteers, aged 32–81 years, Raman spectra were obtained from sun-protected and sun-exposed skin, also three millimeter punch biopsies of sun-exposed skin were collected and analyzed. The Raman spectra were analyzed using principal component analysis and the results were correlated with clinical and histological findings.ResultsThe principal component analysis of the Raman spectra shows that the first principal component (PC1) obtained from the sun-protected skin is related to the age of the subject, which can be taken as a measure of chronological aging, the second (PC2) and fourth (PC4) principal components obtained from Raman spectra of sun-exposed skin are related to the amount of solar elastosis and collagen, respectively.ConclusionIn this work a relationship was found between histological properties of photoaged skin and noninvasive measurements based on Raman and principal components analysis (PCA). These relationships can be used to assess noninvasively the photoinduced damage and chronological characteristics of skin.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00589.x" xmlns="http://purl.org/rss/1.0/"><title>Field melanin mapping of the hairless scalp</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00589.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Field melanin mapping of the hairless scalp</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gérald E. Piérard</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Claudine Piérard-Franchimont</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Pascale Quatresooz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-22T02:02:42.032367-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00589.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00589.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00589.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt589-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Mottled subclinical melanoderma (MSM) is frequently seen on facial skin using the ultraviolet light enhanced visualization (ULEV) method. The corresponding aspect on the hairless scalp remains unknown.</p></div></div><div class="section" id="srt589-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Objective</h3><div class="para"><p>To explore the field distribution of melanin on the scalp of fair-skinned Caucasian subjects.</p></div></div><div class="section" id="srt589-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Method</h3><div class="para"><p>The scalp was examined in 43 men with androgenic alopecia. The Visioscan<sup>®</sup> camera provided the ULEV pictures. Another optical (Visioface<sup>®</sup> Quick) device was used under white light illumination followed by colour contrast enhancement. This was reached after specific computer filtration of the cyan hue wavelengths.</p></div></div><div class="section" id="srt589-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Under white light illumination, the scalp looked normal. MSM patterns were disclosed by both optical procedures as evenly scattered discrete patchy fields of hypermelanosis. The smaller rounded spots were restricted to the lips of the hair infundibula. Larger irregularly shaped spots predominated in the interfollicular areas. A few hypomelanotic spots were scattered over the scalp.</p></div></div><div class="section" id="srt589-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>The present observations based on dual optical methods possibly provide information about a patterned pathobiology of melanocytes on the scalp. The spotty MSM pattern looked similar to the reported aspects on the face. It somewhat resembled the widespread PUVA-induced lentiginosis.</p></div></div>]]></content:encoded><description>BackgroundMottled subclinical melanoderma (MSM) is frequently seen on facial skin using the ultraviolet light enhanced visualization (ULEV) method. The corresponding aspect on the hairless scalp remains unknown.ObjectiveTo explore the field distribution of melanin on the scalp of fair-skinned Caucasian subjects.MethodThe scalp was examined in 43 men with androgenic alopecia. The Visioscan® camera provided the ULEV pictures. Another optical (Visioface® Quick) device was used under white light illumination followed by colour contrast enhancement. This was reached after specific computer filtration of the cyan hue wavelengths.ResultsUnder white light illumination, the scalp looked normal. MSM patterns were disclosed by both optical procedures as evenly scattered discrete patchy fields of hypermelanosis. The smaller rounded spots were restricted to the lips of the hair infundibula. Larger irregularly shaped spots predominated in the interfollicular areas. A few hypomelanotic spots were scattered over the scalp.ConclusionThe present observations based on dual optical methods possibly provide information about a patterned pathobiology of melanocytes on the scalp. The spotty MSM pattern looked similar to the reported aspects on the face. It somewhat resembled the widespread PUVA-induced lentiginosis.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00580.x" xmlns="http://purl.org/rss/1.0/"><title>Dynamic analysis for mental sweating of a group of eccrine sweat glands on a human fingertip by optical coherence tomography</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00580.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Dynamic analysis for mental sweating of a group of eccrine sweat glands on a human fingertip by optical coherence tomography</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Masato Ohmi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Motomu Tanigawa</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yuki Wada</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Masamitsu Haruna</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-16T21:59:57.781597-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00580.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00580.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00580.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt580-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>An important function of skin physiology is mental sweating, where sweating is accelerated via the sympathetic nerve by mental or physical stress externally applied to a volunteer.</p></div></div><div class="section" id="srt580-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Aim</h3><div class="para"><p>Activity of the sympathetic nerve (ASN) is evaluated by quantitative measurement of mental sweating.</p></div></div><div class="section" id="srt580-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Material and Methods</h3><div class="para"><p>Optical coherence tomography (OCT) is highly potential for <em>in vivo</em> observation of human sweating dynamics which affects ASN. We demonstrate dynamic OCT analysis of mental sweating of a group of eccrine sweat glands. The sweating dynamics is tracked simultaneously for 19 sweat glands by time-sequential piled-up en-face OCT images with the frame spacing of 3.3 s. The en-face OCT images of the spiral lumen of the eccrine sweat gland are constructed by data acquisition of the 128 B-mode OCT images.</p></div></div><div class="section" id="srt580-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>It is thus found that the response to mental stress is different for each sweat gland even though the sweat glands are adjacent to each other. Such strong non-uniformity is observed in mental sweating where the amount of excess sweat is different for each sweat gland although the sweat glands are adjacent to each other.</p></div></div><div class="section" id="srt580-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Discussion</h3><div class="para"><p>The non-uniformity should be necessary to adjust as precisely the total amount of excess sweat as possible through the sympathetic nerve in response to strength of the stress.</p></div></div>]]></content:encoded><description>BackgroundAn important function of skin physiology is mental sweating, where sweating is accelerated via the sympathetic nerve by mental or physical stress externally applied to a volunteer.AimActivity of the sympathetic nerve (ASN) is evaluated by quantitative measurement of mental sweating.Material and MethodsOptical coherence tomography (OCT) is highly potential for in vivo observation of human sweating dynamics which affects ASN. We demonstrate dynamic OCT analysis of mental sweating of a group of eccrine sweat glands. The sweating dynamics is tracked simultaneously for 19 sweat glands by time-sequential piled-up en-face OCT images with the frame spacing of 3.3 s. The en-face OCT images of the spiral lumen of the eccrine sweat gland are constructed by data acquisition of the 128 B-mode OCT images.ResultsIt is thus found that the response to mental stress is different for each sweat gland even though the sweat glands are adjacent to each other. Such strong non-uniformity is observed in mental sweating where the amount of excess sweat is different for each sweat gland although the sweat glands are adjacent to each other.DiscussionThe non-uniformity should be necessary to adjust as precisely the total amount of excess sweat as possible through the sympathetic nerve in response to strength of the stress.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00586.x" xmlns="http://purl.org/rss/1.0/"><title>An explorative study of non-invasive ultra-weak photon emission and the anti-oxidative influence of oral zinc sulphate in light-sensitive patients with erythropoietic protoporphyria</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00586.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">An explorative study of non-invasive ultra-weak photon emission and the anti-oxidative influence of oral zinc sulphate in light-sensitive patients with erythropoietic protoporphyria</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anita Birgit Petersen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Peter Alshede Philipsen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hans Christian Wulf</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-16T04:41:58.255992-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00586.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00586.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00586.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt586-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Erythropoietic protoporphyria (EPP) is a rare, inherited disorder of haem biosynthesis owing to deficient ferrochelatase (FECH) and accumulation of protoporphyrin IX (PPIX). This results in acute cutaneous photosensitivity upon light exposure with production of reactive oxygen species (ROS) and ultra-weak photon emission (UPE) as a by-product. We investigated if UPE evaluated the light sensitivity in EPP patients and influence of zinc treatment.</p></div></div><div class="section" id="srt586-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Fourteen EPP patients took zinc sulphate (3 × 200 mg/day) during spring and summer. Using a photomultiplier (PM), UPE was measured from the buttock skin and dorsal hand before and after solar-simulated light (SUN) exposure. Blood samples were analysed routinely for plasma zinc, iron, ferritin, transferrin, haemoglobin, erythrocyte PPIX and Zn-PPIX.</p></div></div><div class="section" id="srt586-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>UPE in EPP patients resembled that seen in healthy individuals. Without treatment, a seasonal decrease was seen from spring to summer in four control patients. However, oral zinc treatment reduced ROS formation significantly regardless of SUN exposure. After SUN exposure, the initial burst was correlated to plasma iron and erythrocyte PPIX. During treatment, an inverse correlation was found between plasma zinc concentration and the initial burst.</p></div></div><div class="section" id="srt586-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Measurements of UPE can be used for monitoring UVA-induced oxidative processes <em>in vivo</em> in the skin of EPP patients.</p></div></div>]]></content:encoded><description>BackgroundErythropoietic protoporphyria (EPP) is a rare, inherited disorder of haem biosynthesis owing to deficient ferrochelatase (FECH) and accumulation of protoporphyrin IX (PPIX). This results in acute cutaneous photosensitivity upon light exposure with production of reactive oxygen species (ROS) and ultra-weak photon emission (UPE) as a by-product. We investigated if UPE evaluated the light sensitivity in EPP patients and influence of zinc treatment.MethodsFourteen EPP patients took zinc sulphate (3 × 200 mg/day) during spring and summer. Using a photomultiplier (PM), UPE was measured from the buttock skin and dorsal hand before and after solar-simulated light (SUN) exposure. Blood samples were analysed routinely for plasma zinc, iron, ferritin, transferrin, haemoglobin, erythrocyte PPIX and Zn-PPIX.ResultsUPE in EPP patients resembled that seen in healthy individuals. Without treatment, a seasonal decrease was seen from spring to summer in four control patients. However, oral zinc treatment reduced ROS formation significantly regardless of SUN exposure. After SUN exposure, the initial burst was correlated to plasma iron and erythrocyte PPIX. During treatment, an inverse correlation was found between plasma zinc concentration and the initial burst.ConclusionMeasurements of UPE can be used for monitoring UVA-induced oxidative processes in vivo in the skin of EPP patients.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00583.x" xmlns="http://purl.org/rss/1.0/"><title>Changes of oxygen content in facial skin before and after cigarette smoking</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00583.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Changes of oxygen content in facial skin before and after cigarette smoking</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Guo-Biao Fan</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Pei-Lan Wu</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Xue-Min Wang</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-14T06:26:18.259087-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00583.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00583.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00583.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt583-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background/purpose</h3><div class="para"><p>Cigarette smoking not only causes systemic health problems, but may also be an underlying cause of premature skin aging. Cigarette smokers frequently have morphological changes in facial skin that may be attributed to reduced oxygen in this region. The purpose of this study was to measure the oxygen content in facial skin before and after smoking.</p></div></div><div class="section" id="srt583-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Twenty-five volunteers participated in this study. Changes in oxygen content of the facial skin were measured before and after 30 min of cigarette smoking. Skin temperature and oxygen content were evaluated in the periorbital and periolar regions.</p></div></div><div class="section" id="srt583-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>There was a significant increase in temperature after smoking. The oxy hemoglobin and partial pressure of oxygen decreased in both the periocular and perioral areas after smoking. There were no changes in deoxy hemoglobin and partial pressure of carbon dioxide at these areas.</p></div></div><div class="section" id="srt583-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Significant changes were seen in temperature and oxygen content after only 30 min of smoking. The results from this study suggest that alterations in the skin temperature and oxygen content in facial skin after smoking may be an underlying cause of premature skin aging.</p></div></div>]]></content:encoded><description>Background/purposeCigarette smoking not only causes systemic health problems, but may also be an underlying cause of premature skin aging. Cigarette smokers frequently have morphological changes in facial skin that may be attributed to reduced oxygen in this region. The purpose of this study was to measure the oxygen content in facial skin before and after smoking.MethodsTwenty-five volunteers participated in this study. Changes in oxygen content of the facial skin were measured before and after 30 min of cigarette smoking. Skin temperature and oxygen content were evaluated in the periorbital and periolar regions.ResultsThere was a significant increase in temperature after smoking. The oxy hemoglobin and partial pressure of oxygen decreased in both the periocular and perioral areas after smoking. There were no changes in deoxy hemoglobin and partial pressure of carbon dioxide at these areas.ConclusionSignificant changes were seen in temperature and oxygen content after only 30 min of smoking. The results from this study suggest that alterations in the skin temperature and oxygen content in facial skin after smoking may be an underlying cause of premature skin aging.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00578.x" xmlns="http://purl.org/rss/1.0/"><title>In vivo investigations on the penetration of various oils and their influence on the skin barrier</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00578.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">In vivo investigations on the penetration of various oils and their influence on the skin barrier</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Patzelt</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Lademann</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. Richter</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. E. Darvin</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. Schanzer</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G. Thiede</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">W. Sterry</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">T. Vergou</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Hauser</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-14T06:26:13.114934-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00578.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00578.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00578.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt578-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>The skin represents a potent barrier to the environment, which can be enhanced by the topical application of skin care products, such as oil and oil-based formulations by moisturizing the skin.</p></div></div><div class="section" id="srt578-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>The aim of this study was the investigation of the penetration behaviour of four vegetable oils and of paraffin oil into the stratum corneum by laser scanning microscopy. In addition, the occlusion capacity of these substances was assessed by transepidermal water loss (TEWL) measurements. Petrolatum served as a positive control for skin occlusion. The study was conducted <em>in vivo</em> and included six healthy volunteers.</p></div></div><div class="section" id="srt578-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Paraffin oil, as well as the vegetable oils, penetrated only into the first upper layers of the stratum corneum. TEWL measurements indicated that the application of the vegetable oils (except jojoba oil) as well as paraffin oil, led to a similar occlusion of the skin surface. The most effective occlusion was found for petrolatum.</p></div></div><div class="section" id="srt578-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>For the investigated oils, a deeper penetration than into the first upper layers of the stratum corneum could be excluded. The decreased TEWL values indicate that the application of the oils leads to a semi-occlusion of the skin surface as it is intended by the use of oils to retain moisture in skin.</p></div></div>]]></content:encoded><description>BackgroundThe skin represents a potent barrier to the environment, which can be enhanced by the topical application of skin care products, such as oil and oil-based formulations by moisturizing the skin.MethodsThe aim of this study was the investigation of the penetration behaviour of four vegetable oils and of paraffin oil into the stratum corneum by laser scanning microscopy. In addition, the occlusion capacity of these substances was assessed by transepidermal water loss (TEWL) measurements. Petrolatum served as a positive control for skin occlusion. The study was conducted in vivo and included six healthy volunteers.ResultsParaffin oil, as well as the vegetable oils, penetrated only into the first upper layers of the stratum corneum. TEWL measurements indicated that the application of the vegetable oils (except jojoba oil) as well as paraffin oil, led to a similar occlusion of the skin surface. The most effective occlusion was found for petrolatum.ConclusionFor the investigated oils, a deeper penetration than into the first upper layers of the stratum corneum could be excluded. The decreased TEWL values indicate that the application of the oils leads to a semi-occlusion of the skin surface as it is intended by the use of oils to retain moisture in skin.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00588.x" xmlns="http://purl.org/rss/1.0/"><title>Methods for evaluation of cosmetic antioxidant capacity</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00588.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Methods for evaluation of cosmetic antioxidant capacity</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anna Ratz-Lyko</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jacek Arct</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Katarzyna Pytkowska</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-14T01:48:31.652915-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00588.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00588.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00588.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Review Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p>The skin as the largest part of human body is one of the main targets for ultraviolet radiation, environmental pollution, toxic chemicals and some metal ions, which share responsibility for the formation of free radicals. The resulting free radicals, both oxygen and nitrogen species are one of the main causes of aging due to impaired regulation of cell respiratory metabolism involving incomplete oxygen reduction in mitochondria and production a superoxide anion, hydroxyl radicals et al. In modern cosmetology to minimize the adverse effects of free radicals, antioxidants, which inhibit free radical reactions, mainly autoxidation processes are used. Currently, not only many cosmetic products containing antioxidants are available, but a large diversity of methods for determination of cosmetics antioxidant activity is also accessible. These methods can be divided into three main groups: <em>in vitro</em>, <em>in vivo</em>, and <em>ex vivo</em> as reported herein. Due to lack of standardization and validation it is necessary to use a variety of methods as well as conditions for those purposes, which are presented to the context.</p></div>]]></content:encoded><description>The skin as the largest part of human body is one of the main targets for ultraviolet radiation, environmental pollution, toxic chemicals and some metal ions, which share responsibility for the formation of free radicals. The resulting free radicals, both oxygen and nitrogen species are one of the main causes of aging due to impaired regulation of cell respiratory metabolism involving incomplete oxygen reduction in mitochondria and production a superoxide anion, hydroxyl radicals et al. In modern cosmetology to minimize the adverse effects of free radicals, antioxidants, which inhibit free radical reactions, mainly autoxidation processes are used. Currently, not only many cosmetic products containing antioxidants are available, but a large diversity of methods for determination of cosmetics antioxidant activity is also accessible. These methods can be divided into three main groups: in vitro, in vivo, and ex vivo as reported herein. Due to lack of standardization and validation it is necessary to use a variety of methods as well as conditions for those purposes, which are presented to the context.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00590.x" xmlns="http://purl.org/rss/1.0/"><title>Reactions of non-immunologic contact urticaria on scalp, face, and back</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00590.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Reactions of non-immunologic contact urticaria on scalp, face, and back</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hongbo Zhai</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yue Zheng</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rolf Fautz</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anne Fuchs</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Howard I. Maibach</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-09T21:36:51.629813-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00590.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00590.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00590.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt590-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>This study compared the reactivity of scalp, face, and back to nonimmunologic contact urticants (NICU) to ascertain relative responsiveness.</p></div></div><div class="section" id="srt590-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Model urticants, benzoic acid (BA) and hexyl nicotinate (HN) with 3 concentrations of each were applied to marked skin of 10 bald males during 6 weeks. One urticant was applied to one side of nasolabial fold, back, and scalp and the other applied to the contralateral side. Reactivity was assessed by visual scores (VS) and biophysical instruments. Subjects ranked skin sensation with a 10-point visual analogue scale.</p></div></div><div class="section" id="srt590-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>With 0.25% HN application, upper back VS significantly (p&lt;0.05) exceeded scalp and back VS also showed significantly (p&lt;0.05) stronger reaction than face at 60 min post-application; however, at 2.5% BA site, VS of face exhibited significantly (p&lt;0.05) higher than back at 15 min post-application but with 0.625% BA site, VS of back was significantly (p&lt;0.05) higher than face. The a* value was significantly (p&lt;0.05) higher on back than scalp with 0.625% BA treatment.</p></div></div><div class="section" id="srt590-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Thus symptoms and measurements vary among sites. Differences may be related to solubility related percutaneous penetration. We encourage investigation into this relatively neglected but clinically important arena, to help explain difference in consumer/patient acceptance of topical formulations.</p></div></div>]]></content:encoded><description>BackgroundThis study compared the reactivity of scalp, face, and back to nonimmunologic contact urticants (NICU) to ascertain relative responsiveness.MethodsModel urticants, benzoic acid (BA) and hexyl nicotinate (HN) with 3 concentrations of each were applied to marked skin of 10 bald males during 6 weeks. One urticant was applied to one side of nasolabial fold, back, and scalp and the other applied to the contralateral side. Reactivity was assessed by visual scores (VS) and biophysical instruments. Subjects ranked skin sensation with a 10-point visual analogue scale.ResultsWith 0.25% HN application, upper back VS significantly (p&lt;0.05) exceeded scalp and back VS also showed significantly (p&lt;0.05) stronger reaction than face at 60 min post-application; however, at 2.5% BA site, VS of face exhibited significantly (p&lt;0.05) higher than back at 15 min post-application but with 0.625% BA site, VS of back was significantly (p&lt;0.05) higher than face. The a* value was significantly (p&lt;0.05) higher on back than scalp with 0.625% BA treatment.ConclusionThus symptoms and measurements vary among sites. Differences may be related to solubility related percutaneous penetration. We encourage investigation into this relatively neglected but clinically important arena, to help explain difference in consumer/patient acceptance of topical formulations.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00581.x" xmlns="http://purl.org/rss/1.0/"><title>In vivo reflectance confocal microscopy for varicella prompt diagnosis and treatment in a severely immunosuppressed patient</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00581.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">In vivo reflectance confocal microscopy for varicella prompt diagnosis and treatment in a severely immunosuppressed patient</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Leonardo Spagnol Abraham</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mariana Carvalho Costa</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marina Agozzino</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Beatrice Amorosi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Carlo Cota</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marco Ardigo</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-11-09T21:36:42.937167-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00581.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00581.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00581.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00572.x" xmlns="http://purl.org/rss/1.0/"><title>Where's the naevus? Inter-operator variability in the localization of melanocytic lesion border</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00572.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Where's the naevus? Inter-operator variability in the localization of melanocytic lesion border</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anna Belloni Fortina</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Enoch Peserico</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Alberto Silletti</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Edoardo Zattra</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-10-28T05:52:58.122333-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00572.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00572.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00572.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt572-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background: </h3><div class="para"><p>The first step in the analysis of a dermatoscopically imaged melanocytic lesion is segmentation – informally, isolating those points in the image belonging to the lesion from those belonging to the surrounding non-lesional skin. Although typically studied in the context of automated analysis, segmentation is a necessary step even for human operators who plan to evaluate quantitative features of a lesion (such as diameter or asymmetry).</p></div></div><div class="section" id="srt572-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods: </h3><div class="para"><p>In a double blind evaluation of the segmentation of 77 digital dermatoscopic images, we observed a significant inter-operator variability.</p></div></div><div class="section" id="srt572-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results: </h3><div class="para"><p>The area of the disagreement region was on average 15.28% of the area of the lesion itself, and in 10% of the cases it was more than 28%. More experienced dermatologists showed greater agreement among themselves than with less experienced dermatologists, and a slight tendency toward ‘tighter’ segmentations.</p></div></div><div class="section" id="srt572-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion: </h3><div class="para"><p>The evaluation methodology addresses a number of crucial difficulties encountered in previous studies and may be of independent interest. Our results underscore the necessity of taking into account inter-operator variability in large epidemiological studies, in particular those involving less experienced dermatologists, and of striving toward techniques allowing greater standardization and replicability in the evaluation of the fundamental visual parameters of lesions.</p></div></div>]]></content:encoded><description>Background: The first step in the analysis of a dermatoscopically imaged melanocytic lesion is segmentation – informally, isolating those points in the image belonging to the lesion from those belonging to the surrounding non-lesional skin. Although typically studied in the context of automated analysis, segmentation is a necessary step even for human operators who plan to evaluate quantitative features of a lesion (such as diameter or asymmetry).Methods: In a double blind evaluation of the segmentation of 77 digital dermatoscopic images, we observed a significant inter-operator variability.Results: The area of the disagreement region was on average 15.28% of the area of the lesion itself, and in 10% of the cases it was more than 28%. More experienced dermatologists showed greater agreement among themselves than with less experienced dermatologists, and a slight tendency toward ‘tighter’ segmentations.Conclusion: The evaluation methodology addresses a number of crucial difficulties encountered in previous studies and may be of independent interest. Our results underscore the necessity of taking into account inter-operator variability in large epidemiological studies, in particular those involving less experienced dermatologists, and of striving toward techniques allowing greater standardization and replicability in the evaluation of the fundamental visual parameters of lesions.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00560.x" xmlns="http://purl.org/rss/1.0/"><title>Skin surface hydration decreases rapidly during long distance flights</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00560.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Skin surface hydration decreases rapidly during long distance flights</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sabine Guéhenneux</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sophie Gardinier</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Frederique Morizot</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Isabelle Fur</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Erwin Tschachler</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-10-17T23:30:48.324817-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00560.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00560.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00560.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt560-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Introduction</h3><div class="para"><p>Dehydration of the stratum corneum leads to sensations and symptoms of ‘dry skin’ such as skin tightness and itchiness. As these complaints are frequently experienced by airline travellers, the aim of this study was to investigate the changes in skin surface hydration during long distance flights.</p></div></div><div class="section" id="srt560-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>The study was performed on four healthy Caucasian, and on four Japanese women aged 29–39 years, travelling on long distance flights. They had stopped using skin care products at least 12 h before, and did not apply them during the flights. The air temperature and relative humidity inside the cabin, as well as skin capacitance of the face and forearm of participants, were registered at several time points before and during the flights.</p></div></div><div class="section" id="srt560-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Relative humidity of the aircraft cabin dropped to levels below 10% within 2 h after take-off and stayed at this value throughout the flight. Skin capacitance decreased rapidly on both the face and forearms with most pronounced changes on the cheeks where it decreased by up to 37%.</p></div></div><div class="section" id="srt560-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Our results demonstrate that during long distance flights, the aircraft cabin environment leads to a rapid decrease in stratum corneum hydration, an alteration, which probably accounts for the discomfort experienced by long distance aircraft travellers.</p></div></div>]]></content:encoded><description>IntroductionDehydration of the stratum corneum leads to sensations and symptoms of ‘dry skin’ such as skin tightness and itchiness. As these complaints are frequently experienced by airline travellers, the aim of this study was to investigate the changes in skin surface hydration during long distance flights.MethodsThe study was performed on four healthy Caucasian, and on four Japanese women aged 29–39 years, travelling on long distance flights. They had stopped using skin care products at least 12 h before, and did not apply them during the flights. The air temperature and relative humidity inside the cabin, as well as skin capacitance of the face and forearm of participants, were registered at several time points before and during the flights.ResultsRelative humidity of the aircraft cabin dropped to levels below 10% within 2 h after take-off and stayed at this value throughout the flight. Skin capacitance decreased rapidly on both the face and forearms with most pronounced changes on the cheeks where it decreased by up to 37%.ConclusionOur results demonstrate that during long distance flights, the aircraft cabin environment leads to a rapid decrease in stratum corneum hydration, an alteration, which probably accounts for the discomfort experienced by long distance aircraft travellers.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00552.x" xmlns="http://purl.org/rss/1.0/"><title>A comparison between laser-doppler imaging and colorimetry in the assessment of scarring: “a pilot study”</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00552.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A comparison between laser-doppler imaging and colorimetry in the assessment of scarring: “a pilot study”</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wouter Peeters</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mieke Anthonissen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">An Deliaert</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rene Van der Hulst</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Eric Van den Kerckhove</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-10-13T22:51:49.433918-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00552.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00552.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00552.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt552-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background:</h3><div class="para"><p>This cross-sectional pilot-study investigated the reproducibility of the LDI (Moor-LDI-B2; Moor Instruments) and the chromameter (Minolta chromameter CR-300) when used in scar assessment.</p></div></div><div class="section" id="srt552-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods:</h3><div class="para"><p>Twenty-seven scars in 14 subjects were included between January and June 2003. One observer performed two times both measurements with 10 min apart. The intra-observer agreement is quantified by means of the intra-class correlations (ICC) and the standard errors of measurement (SEM) for both the LDI and the chromameter.</p></div></div><div class="section" id="srt552-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results:</h3><div class="para"><p>Ignoring one outlier, the ICC of the LDI = 0.856 and the SEM = 34.56. The chromameter shows a better reproducibility with an ICC of 0.93 and a SEM of 0.79.</p></div></div><div class="section" id="srt552-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion:</h3><div class="para"><p>This pilot-study with a limited number of measurements shows a moderate reproducibility of the LDI compared to the chromameter measurements, in the assessment of respectively flux and redness in scars.</p></div></div>]]></content:encoded><description>Background:This cross-sectional pilot-study investigated the reproducibility of the LDI (Moor-LDI-B2; Moor Instruments) and the chromameter (Minolta chromameter CR-300) when used in scar assessment.Methods:Twenty-seven scars in 14 subjects were included between January and June 2003. One observer performed two times both measurements with 10 min apart. The intra-observer agreement is quantified by means of the intra-class correlations (ICC) and the standard errors of measurement (SEM) for both the LDI and the chromameter.Results:Ignoring one outlier, the ICC of the LDI = 0.856 and the SEM = 34.56. The chromameter shows a better reproducibility with an ICC of 0.93 and a SEM of 0.79.Conclusion:This pilot-study with a limited number of measurements shows a moderate reproducibility of the LDI compared to the chromameter measurements, in the assessment of respectively flux and redness in scars.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00576.x" xmlns="http://purl.org/rss/1.0/"><title>Tensegrity and plasma for skin regeneration</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00576.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Tensegrity and plasma for skin regeneration</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Stefania Pacini</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gabriele Morucci</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marco Ruggiero</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Massimo Gulisano</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Tiziana Punzi</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-10-10T22:23:14.996393-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00576.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00576.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00576.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt576-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Mechanical stresses induce variations in tissue tensegrity leading to cell proliferation and differentiation thus contributing to tissue remodelling. Besides mechanical forces, skin remodelling may be induced by the application of plasma, a new type of energy delivery resulting in controlled heat damage. Here we demonstrate that mechanical stress induced by the application of vacuum increases the efficacy of plasma in skin regeneration treatment.</p></div></div><div class="section" id="srt576-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Vacuum alone and vacuum plus plasma at different energies were applied to rat skin and biopsies collected at different time intervals after treatments. Skin integrity, collagen arrangement, inflammation and myofibroblast differentiation were assessed by Masson's trichrome staining. Procollagen synthesis was evaluated by immunohistochemistry.</p></div></div><div class="section" id="srt576-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Vacuum alone induced significant and temporary alterations in the distribution of collagen bundles, with concomitant procollagen synthesis in the dermis; no myofibroblasts and no signs of inflammation were observed. Vacuum plus plasma determined an important spatial modification of collagen bundles, more intense than vacuum or plasma alone. Significant increase of procollagen synthesis, numerous myofibroblasts but slight sign of inflammation appeared after the treatment.</p></div></div><div class="section" id="srt576-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Vacuum mechanically stimulated fibroblasts, producing changes in collagen arrangement and procollagen synthesis. Plasma led to the same effects through thermal damage. Application of a combined treatment consisting in vacuum plus plasma induced more remarkable effects on skin regeneration with relatively low plasma energies and no relevant side effects.</p></div></div>]]></content:encoded><description>BackgroundMechanical stresses induce variations in tissue tensegrity leading to cell proliferation and differentiation thus contributing to tissue remodelling. Besides mechanical forces, skin remodelling may be induced by the application of plasma, a new type of energy delivery resulting in controlled heat damage. Here we demonstrate that mechanical stress induced by the application of vacuum increases the efficacy of plasma in skin regeneration treatment.MethodsVacuum alone and vacuum plus plasma at different energies were applied to rat skin and biopsies collected at different time intervals after treatments. Skin integrity, collagen arrangement, inflammation and myofibroblast differentiation were assessed by Masson's trichrome staining. Procollagen synthesis was evaluated by immunohistochemistry.ResultsVacuum alone induced significant and temporary alterations in the distribution of collagen bundles, with concomitant procollagen synthesis in the dermis; no myofibroblasts and no signs of inflammation were observed. Vacuum plus plasma determined an important spatial modification of collagen bundles, more intense than vacuum or plasma alone. Significant increase of procollagen synthesis, numerous myofibroblasts but slight sign of inflammation appeared after the treatment.ConclusionVacuum mechanically stimulated fibroblasts, producing changes in collagen arrangement and procollagen synthesis. Plasma led to the same effects through thermal damage. Application of a combined treatment consisting in vacuum plus plasma induced more remarkable effects on skin regeneration with relatively low plasma energies and no relevant side effects.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00554.x" xmlns="http://purl.org/rss/1.0/"><title>Skin hydration and cooling effect produced by the Voltaren® vehicle gel</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00554.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Skin hydration and cooling effect produced by the Voltaren® vehicle gel</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Agnes M. Hug</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Thomas Schmidts</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jens Kuhlmann</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Dörte Segger</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Grigorios Fotopoulos</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Johanna Heinzerling</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-09-15T06:58:34.802685-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00554.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00554.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00554.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt554-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Voltaren vehicle gel is the carrier substance of the topical Voltaren products. This vehicle gel is especially formulated to be easily applied on the skin, while providing some sensory benefits. The present study aims to substantiate the widely perceived hydrating and cooling effect of Voltaren vehicle gel.</p></div></div><div class="section" id="srt554-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Volar forearm skin hydration and transepidermal water loss (TEWL) were measured and user satisfaction was evaluated by questionnaires, after application in 31 healthy, female volunteers. The cooling effect was investigated for 40 min with thermal imaging on 12 forearm sites of six healthy subjects.</p></div></div><div class="section" id="srt554-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Voltaren vehicle gel application increased skin hydration by 13.1% (<em>P</em> = 0.0002) when compared with the untreated site, 8 h after the final treatment after 2 weeks. TEWL decreased on both treated (0.37 g/m<sup>2</sup>/h) and untreated (0.74 g/m<sup>2</sup>/h) forearm sites after 2 weeks (8 h after last treatment), demonstrating a relative increase of 6.5% in water loss. Voltaren vehicle gel application resulted in a rapid reduction of skin surface temperature by 5.1°C after only 3 min with an average maximum reduction of 5.8°C after 10 min. The cooling effect was experienced by 94% subjects, while 74% felt that their skin became softer. No adverse events, including skin irritation, were reported during the study and by the 37 participants.</p></div></div><div class="section" id="srt554-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>This study showed a statistically significant increase in skin hydration as well as a rapid cooling effect lasting approximately 30 min, after application of Voltaren vehicle gel. The small relative increase in water loss may be attributed to an additional skin surface water loss secondary to the increased water content brought into the skin by the Voltaren vehicle gel. The use did not induce any skin irritation and was found acceptable to use by the majority of participants.</p></div></div>]]></content:encoded><description>BackgroundVoltaren vehicle gel is the carrier substance of the topical Voltaren products. This vehicle gel is especially formulated to be easily applied on the skin, while providing some sensory benefits. The present study aims to substantiate the widely perceived hydrating and cooling effect of Voltaren vehicle gel.MethodsVolar forearm skin hydration and transepidermal water loss (TEWL) were measured and user satisfaction was evaluated by questionnaires, after application in 31 healthy, female volunteers. The cooling effect was investigated for 40 min with thermal imaging on 12 forearm sites of six healthy subjects.ResultsVoltaren vehicle gel application increased skin hydration by 13.1% (P = 0.0002) when compared with the untreated site, 8 h after the final treatment after 2 weeks. TEWL decreased on both treated (0.37 g/m2/h) and untreated (0.74 g/m2/h) forearm sites after 2 weeks (8 h after last treatment), demonstrating a relative increase of 6.5% in water loss. Voltaren vehicle gel application resulted in a rapid reduction of skin surface temperature by 5.1°C after only 3 min with an average maximum reduction of 5.8°C after 10 min. The cooling effect was experienced by 94% subjects, while 74% felt that their skin became softer. No adverse events, including skin irritation, were reported during the study and by the 37 participants.ConclusionThis study showed a statistically significant increase in skin hydration as well as a rapid cooling effect lasting approximately 30 min, after application of Voltaren vehicle gel. The small relative increase in water loss may be attributed to an additional skin surface water loss secondary to the increased water content brought into the skin by the Voltaren vehicle gel. The use did not induce any skin irritation and was found acceptable to use by the majority of participants.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00558.x" xmlns="http://purl.org/rss/1.0/"><title>Using optical coherence tomography for the longitudinal non-invasive evaluation of epidermal thickness in a murine model of chronic skin inflammation</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00558.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Using optical coherence tomography for the longitudinal non-invasive evaluation of epidermal thickness in a murine model of chronic skin inflammation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rachel Silver</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Amy Helms</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wen Fu</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hui Wang</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Doina Diaconu</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Candace M. Loyd</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Andrew M. Rollins</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Nicole L. Ward</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-09-14T04:34:24.338243-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00558.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00558.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00558.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt558-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Non-invasive methods are desirable for longitudinal studies examining drug efficacy and disease resolution defined as decreases in epidermal thickness in mouse models of psoriasiform skin disease. This would eliminate the need for either sacrificing animals or collecting serial skin biopsies to evaluate changes in disease progression during an individual study. The quantitation of epidermal thickness using optical coherence tomography (OCT) provides an alternative to traditional histology techniques.</p></div></div><div class="section" id="srt558-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Using the KC-Tie2 doxycycline-repressible psoriasiform skin disease mouse model, OCT imaging was completed on diseased back skin of adult KC-Tie2 (<em>n</em> = 3–4) and control (<em>n</em> = 3–4) mice, followed immediately by the surgical excision of the same region for histologic analyses. Animals were then treated with doxycycline to suppress transgene expression and to reverse the skin disease and additional OCT images and tissues were collected 2 and 4 weeks following. Epidermal thickness was measured using OCT and histology.</p></div></div><div class="section" id="srt558-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Optical coherence tomography and histology both demonstrated that KC-Tie2 mice had significantly thicker epidermis (~4-fold; <em>P</em> &lt; 0.0001) than control animals. By 2 weeks following gene repression, decreases in epidermal thickness were observed using both OCT and histology, and were sustained through 4 weeks. Correlation analyses between histology and OCT values at all time points and in all animals revealed high significance (<em>R</em><sup>2</sup> = 0.78); with correlation being highest in KC-Tie2 mice (<em>R</em><sup>2</sup> = 0.92) compared to control animals (<em>R</em><sup>2</sup> = 0.16).</p></div></div><div class="section" id="srt558-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Non-invasive OCT imaging provided similar values as those collected using standard histologic measures in thick skin of KC-Tie2 mice but became less reliable in thinner control mouse skin, possibly reflecting limitations in resolution of OCT. Future advances in resolution of OCT may improve and allow greater accuracy of epidermal thickness measurements.</p></div></div>]]></content:encoded><description>BackgroundNon-invasive methods are desirable for longitudinal studies examining drug efficacy and disease resolution defined as decreases in epidermal thickness in mouse models of psoriasiform skin disease. This would eliminate the need for either sacrificing animals or collecting serial skin biopsies to evaluate changes in disease progression during an individual study. The quantitation of epidermal thickness using optical coherence tomography (OCT) provides an alternative to traditional histology techniques.MethodsUsing the KC-Tie2 doxycycline-repressible psoriasiform skin disease mouse model, OCT imaging was completed on diseased back skin of adult KC-Tie2 (n = 3–4) and control (n = 3–4) mice, followed immediately by the surgical excision of the same region for histologic analyses. Animals were then treated with doxycycline to suppress transgene expression and to reverse the skin disease and additional OCT images and tissues were collected 2 and 4 weeks following. Epidermal thickness was measured using OCT and histology.ResultsOptical coherence tomography and histology both demonstrated that KC-Tie2 mice had significantly thicker epidermis (~4-fold; P &lt; 0.0001) than control animals. By 2 weeks following gene repression, decreases in epidermal thickness were observed using both OCT and histology, and were sustained through 4 weeks. Correlation analyses between histology and OCT values at all time points and in all animals revealed high significance (R2 = 0.78); with correlation being highest in KC-Tie2 mice (R2 = 0.92) compared to control animals (R2 = 0.16).ConclusionNon-invasive OCT imaging provided similar values as those collected using standard histologic measures in thick skin of KC-Tie2 mice but became less reliable in thinner control mouse skin, possibly reflecting limitations in resolution of OCT. Future advances in resolution of OCT may improve and allow greater accuracy of epidermal thickness measurements.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00553.x" xmlns="http://purl.org/rss/1.0/"><title>Cosmetic efficacy evaluation of an anti-acne cream using the 3D image analysis system</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00553.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Cosmetic efficacy evaluation of an anti-acne cream using the 3D image analysis system</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kyung Min Choi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">So Jeong Kim</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ji Hwoon Baek</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Seung-Joo Kang</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yong Chool Boo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jae Sook Koh</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-09-06T05:06:23.069167-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00553.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00553.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00553.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Announcement</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt553-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background/purpose</h3><div class="para"><p>Acne is a skin disease which accompanies pathological and morphological changes. Although acne severity is scored by clinicians based on pathological status, aesthetic aspect of acne symptom is also concerned by patients. This study was conducted to examine the usefulness of a 3D image analysis method for the cosmetic efficacy evaluation of an anti-acne cream.</p></div></div><div class="section" id="srt553-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Twenty-one healthy volunteers with acne lesions were recruited for the study and treated with an ‘anti-acne cream’ for 4 weeks. Acne symptoms on the facial skin were graded by the visual evaluation of photographs taken before and after the treatment. Skin color of acne lesions was and measured by a spectrophotometer. In addition, a 3D image analysis system was used to quantify skin surface roughness and acne volumes.</p></div></div><div class="section" id="srt553-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Both visual and spectrophotometric assessments of acne lesions provided similar results indicating that the cream treatment improved acne symptoms significantly. The 3D image analysis of acne lesions confirmed that the cream treatment decreased skin surface roughness and acne volumes.</p></div></div><div class="section" id="srt553-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>The current study demonstrated that the 3D image-based analysis of the skin may be useful for the quantification of acne symptoms of cosmetic relevance.</p></div></div>]]></content:encoded><description>Background/purposeAcne is a skin disease which accompanies pathological and morphological changes. Although acne severity is scored by clinicians based on pathological status, aesthetic aspect of acne symptom is also concerned by patients. This study was conducted to examine the usefulness of a 3D image analysis method for the cosmetic efficacy evaluation of an anti-acne cream.MethodsTwenty-one healthy volunteers with acne lesions were recruited for the study and treated with an ‘anti-acne cream’ for 4 weeks. Acne symptoms on the facial skin were graded by the visual evaluation of photographs taken before and after the treatment. Skin color of acne lesions was and measured by a spectrophotometer. In addition, a 3D image analysis system was used to quantify skin surface roughness and acne volumes.ResultsBoth visual and spectrophotometric assessments of acne lesions provided similar results indicating that the cream treatment improved acne symptoms significantly. The 3D image analysis of acne lesions confirmed that the cream treatment decreased skin surface roughness and acne volumes.ConclusionThe current study demonstrated that the 3D image-based analysis of the skin may be useful for the quantification of acne symptoms of cosmetic relevance.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00575.x" xmlns="http://purl.org/rss/1.0/"><title>Quantitative method for measuring therapeutic efficacy of the 308 nm excimer laser for vitiligo</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00575.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Quantitative method for measuring therapeutic efficacy of the 308 nm excimer laser for vitiligo</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Tae Seok Oh</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Onseok Lee</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jeong Eun Kim</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sang Wook Son</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Chil Hwan Oh</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-09-06T04:58:57.173617-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00575.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00575.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00575.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt575-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>There are several available treatments for vitiligo, but measurement of their therapeutic efficacy is not standardized and is somewhat arbitrary based largely on the global impression of the overall response. The purpose of this study was to develop a quantitative method for evaluating the treatment response of vitiligo measuring changes in area using digital image analysis. We applied this parametric model to the evaluation of efficacy of the 308 nm excimer laser.</p></div></div><div class="section" id="srt575-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>This study was a retrospective study, designed as a before and after trial with a single arm. A total of 18 patients were enrolled who had been treated with a 308 nm excimer laser as monotherapy twice a week for 20 sessions. The repigmentation percentage was calculated by measuring changes in area before and after treatment using digital image analysis and graded on a five-point ordinal scale [global assessment scale (GAS)]. GAS was also measured by physician and patient for comparison with our estimates. Additional GASs were also measured by four different evaluators for inter-rater variability.</p></div></div><div class="section" id="srt575-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>The mean repigmentation percentage after treatment was 45.3% (range, 0.7–100%). The changes in area after treatment were statistically significant (<em>P </em>&lt; 0.05). A substantial agreement of outcomes was observed between physicians and digital image analysis (κ<sub>w</sub> = 0.78), but lower agreement was observed between patients and digital image analysis (κ<sub>w</sub> = 0.49). The inter-rater variability for GAS was substantially low (Krippendorff's α = 79.3%).</p></div></div><div class="section" id="srt575-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Measurement of changes in area using digital image analysis could be used as a quantitative method in evaluating efficacy of treatment for vitiligo. Because vitiligo lesions can occur in any location with various shapes and sizes, digital image analysis would be a more objective method for measuring treatment response than a GAS.</p></div></div>]]></content:encoded><description>BackgroundThere are several available treatments for vitiligo, but measurement of their therapeutic efficacy is not standardized and is somewhat arbitrary based largely on the global impression of the overall response. The purpose of this study was to develop a quantitative method for evaluating the treatment response of vitiligo measuring changes in area using digital image analysis. We applied this parametric model to the evaluation of efficacy of the 308 nm excimer laser.MethodsThis study was a retrospective study, designed as a before and after trial with a single arm. A total of 18 patients were enrolled who had been treated with a 308 nm excimer laser as monotherapy twice a week for 20 sessions. The repigmentation percentage was calculated by measuring changes in area before and after treatment using digital image analysis and graded on a five-point ordinal scale [global assessment scale (GAS)]. GAS was also measured by physician and patient for comparison with our estimates. Additional GASs were also measured by four different evaluators for inter-rater variability.ResultsThe mean repigmentation percentage after treatment was 45.3% (range, 0.7–100%). The changes in area after treatment were statistically significant (P &lt; 0.05). A substantial agreement of outcomes was observed between physicians and digital image analysis (κw = 0.78), but lower agreement was observed between patients and digital image analysis (κw = 0.49). The inter-rater variability for GAS was substantially low (Krippendorff's α = 79.3%).ConclusionMeasurement of changes in area using digital image analysis could be used as a quantitative method in evaluating efficacy of treatment for vitiligo. Because vitiligo lesions can occur in any location with various shapes and sizes, digital image analysis would be a more objective method for measuring treatment response than a GAS.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00569.x" xmlns="http://purl.org/rss/1.0/"><title>Three-phase general border detection method for dermoscopy images using non-uniform illumination correction</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00569.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Three-phase general border detection method for dermoscopy images using non-uniform illumination correction</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kerri-Ann Norton</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hitoshi Iyatomi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Emre Celebi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sumiko Ishizaki</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mizuki Sawada</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Reiko Suzaki</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ken Kobayashi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Masaru Tanaka</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Koichi Ogawa</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-09-06T04:58:45.537761-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00569.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00569.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00569.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt569-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Computer-aided diagnosis of dermoscopy images has shown great promise in developing a quantitative, objective way of classifying skin lesions. An important step in the classification process is lesion segmentation. Many studies have been successful in segmenting melanocytic skin lesions (MSLs), but few have focused on non-melanocytic skin lesions (NoMSLs), as the wide variety of lesions makes accurate segmentation difficult.</p></div></div><div class="section" id="srt569-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>We developed an automatic segmentation program for detecting borders of skin lesions in dermoscopy images. The method consists of a pre-processing phase, general lesion segmentation phase, including illumination correction, and bright region segmentation phase.</p></div></div><div class="section" id="srt569-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>We tested our method on a set of 107 NoMSLs and a set of 319 MSLs. Our method achieved precision/recall scores of 84.5% and 88.5% for NoMSLs, and 93.9% and 93.8% for MSLs, in comparison with manual extractions from four or five dermatologists.</p></div></div><div class="section" id="srt569-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>The accuracy of our method was competitive or better than five recently published methods. Our new method is the first method for detecting borders of both non-melanocytic and melanocytic skin lesions.</p></div></div>]]></content:encoded><description>BackgroundComputer-aided diagnosis of dermoscopy images has shown great promise in developing a quantitative, objective way of classifying skin lesions. An important step in the classification process is lesion segmentation. Many studies have been successful in segmenting melanocytic skin lesions (MSLs), but few have focused on non-melanocytic skin lesions (NoMSLs), as the wide variety of lesions makes accurate segmentation difficult.MethodsWe developed an automatic segmentation program for detecting borders of skin lesions in dermoscopy images. The method consists of a pre-processing phase, general lesion segmentation phase, including illumination correction, and bright region segmentation phase.ResultsWe tested our method on a set of 107 NoMSLs and a set of 319 MSLs. Our method achieved precision/recall scores of 84.5% and 88.5% for NoMSLs, and 93.9% and 93.8% for MSLs, in comparison with manual extractions from four or five dermatologists.ConclusionThe accuracy of our method was competitive or better than five recently published methods. Our new method is the first method for detecting borders of both non-melanocytic and melanocytic skin lesions.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00563.x" xmlns="http://purl.org/rss/1.0/"><title>Determination of the protection efficacy and homogeneity of the distribution of sunscreens applied onto skin pre-treated with cosmetic products</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00563.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Determination of the protection efficacy and homogeneity of the distribution of sunscreens applied onto skin pre-treated with cosmetic products</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hans-Jürgen Weigmann</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Maude Suisse Sainte Claire</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sabine Schanzer</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Alexa Patzelt</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Martina Meinke</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Christina Antoniou</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wolfram Sterry</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jürgen Lademann</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-09-06T04:57:41.76254-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00563.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00563.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00563.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt563-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>The efficacy of sunscreens depends decisively on the homogeneity of its distribution on the skin surface, which is sensitively reflected by two spectroscopic data – the factor of inhomogeneity and the sum transmission – measured after tape stripping. The aim of this study was to investigate the influence of a skin pre-treatment with body lotion on the layout of the formulations.</p></div></div><div class="section" id="srt563-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Six healthy volunteers were pre-treated using the body lotion, Nivea Body (Beiersdorf AG, Hamburg, Germany). The sunscreen was an oil/water (o/w) emulsion, Roc SPF 8 (RoC SA, Paris, France). The tape stripped <em>tesa</em> films were measured with a modified UV/VIS spectrometer Lambda 5 (PerkinElmer, Frankfurt/Main, Germany), the data of which were used to calculate both measurands.</p></div></div><div class="section" id="srt563-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>The obtained results made clear that the original spectroscopic data must be corrected taking into account the changed amounts of horny layer particles removed with the individual tape strips after pre-treatment. As a consequence of the correction, the factors of inhomogeneity as well as the sum transmissions confirm a more homogeneous distribution of the applied sunscreen.</p></div></div><div class="section" id="srt563-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>The findings confirm that the applied method is well suited to obtain information on the distribution of topically applied substances, and furthermore that the influence of the pre-treatment of the skin with the body lotion enhances the homogeneity of distribution and thus the sunscreen efficacy.</p></div></div>]]></content:encoded><description>BackgroundThe efficacy of sunscreens depends decisively on the homogeneity of its distribution on the skin surface, which is sensitively reflected by two spectroscopic data – the factor of inhomogeneity and the sum transmission – measured after tape stripping. The aim of this study was to investigate the influence of a skin pre-treatment with body lotion on the layout of the formulations.MethodsSix healthy volunteers were pre-treated using the body lotion, Nivea Body (Beiersdorf AG, Hamburg, Germany). The sunscreen was an oil/water (o/w) emulsion, Roc SPF 8 (RoC SA, Paris, France). The tape stripped tesa films were measured with a modified UV/VIS spectrometer Lambda 5 (PerkinElmer, Frankfurt/Main, Germany), the data of which were used to calculate both measurands.ResultsThe obtained results made clear that the original spectroscopic data must be corrected taking into account the changed amounts of horny layer particles removed with the individual tape strips after pre-treatment. As a consequence of the correction, the factors of inhomogeneity as well as the sum transmissions confirm a more homogeneous distribution of the applied sunscreen.ConclusionThe findings confirm that the applied method is well suited to obtain information on the distribution of topically applied substances, and furthermore that the influence of the pre-treatment of the skin with the body lotion enhances the homogeneity of distribution and thus the sunscreen efficacy.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00556.x" xmlns="http://purl.org/rss/1.0/"><title>Targeted 307 nm UVB-phototherapy in psoriasis. A pilot study comparing a 307 nm excimer light with topical dithranol</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00556.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Targeted 307 nm UVB-phototherapy in psoriasis. A pilot study comparing a 307 nm excimer light with topical dithranol</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Uwe Wollina</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">André Koch</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Armin Scheibe</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bernd Seme</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ingolf Streit</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wolf-Dieter Schmidt</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-09-04T21:05:23.996234-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00556.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00556.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00556.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt556-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Phototherapy is a cornerstone in treatment of moderate-to-severe psoriasis. Narrow-band UVB has been shown to be a potent therapeutic tool. To reduce the potential carcinogenic risk, targeted phototherapy has been developed using excimer lasers or excimer light devices (ELD).</p></div></div><div class="section" id="srt556-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Objective</h3><div class="para"><p>The role of excimer light therapy in practice and modes of action are not completely understood. We wanted to investigate a 307 nm ELD for plaque psoriasis in comparison with topical dithranol therapy twice daily.</p></div></div><div class="section" id="srt556-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>We conducted a pilot trial in 21 adult patients with moderate plaque-type psoriasis. Two target lesions of comparable size and plaque-modified Psoriasis Activity and Severity Index (PSI) scores were selected. Lesion A was treated three times using a newly developed 307 nm ELD. Lesion B was treated twice daily with dithranol ointment. The mean period of treatment was 9 days. Clinical evaluation included PSI scores, safety, time needed to treat, and patient's satisfaction. In addition, fluorescence-remission imaging technique was used for objective evaluation.</p></div></div><div class="section" id="srt556-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Both treatments improved the PSI score (mean 3.0 points). The treatments were safe but ELD was more convenient for patients. The time needed to treat the target lesion was significantly shorter with ELD. Targeted UVB therapy normalized NADH fluorescence in lesional skin.</p></div></div><div class="section" id="srt556-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusions</h3><div class="para"><p>The 307 nm excimer light therapy for plaque type psoriasis was equipotent to twice daily topical dithranol. Efficacy, safety, and convenience suggest that targeted UVB therapy with quasi monochromatic light is a new useful treatment option for patients with limited psoriatic plaques.</p></div></div>]]></content:encoded><description>BackgroundPhototherapy is a cornerstone in treatment of moderate-to-severe psoriasis. Narrow-band UVB has been shown to be a potent therapeutic tool. To reduce the potential carcinogenic risk, targeted phototherapy has been developed using excimer lasers or excimer light devices (ELD).ObjectiveThe role of excimer light therapy in practice and modes of action are not completely understood. We wanted to investigate a 307 nm ELD for plaque psoriasis in comparison with topical dithranol therapy twice daily.MethodsWe conducted a pilot trial in 21 adult patients with moderate plaque-type psoriasis. Two target lesions of comparable size and plaque-modified Psoriasis Activity and Severity Index (PSI) scores were selected. Lesion A was treated three times using a newly developed 307 nm ELD. Lesion B was treated twice daily with dithranol ointment. The mean period of treatment was 9 days. Clinical evaluation included PSI scores, safety, time needed to treat, and patient's satisfaction. In addition, fluorescence-remission imaging technique was used for objective evaluation.ResultsBoth treatments improved the PSI score (mean 3.0 points). The treatments were safe but ELD was more convenient for patients. The time needed to treat the target lesion was significantly shorter with ELD. Targeted UVB therapy normalized NADH fluorescence in lesional skin.ConclusionsThe 307 nm excimer light therapy for plaque type psoriasis was equipotent to twice daily topical dithranol. Efficacy, safety, and convenience suggest that targeted UVB therapy with quasi monochromatic light is a new useful treatment option for patients with limited psoriatic plaques.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00571.x" xmlns="http://purl.org/rss/1.0/"><title>A possible melanoma discrimination index based on hyperspectral data: a pilot study</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00571.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A possible melanoma discrimination index based on hyperspectral data: a pilot study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Takashi Nagaoka</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Atsushi Nakamura</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Haruka Okutani</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yoshio Kiyohara</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Takayuki Sota</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-08-30T23:25:26.78256-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00571.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00571.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00571.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt571-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Early detection and proper excision of the primary lesions of malignant melanoma (MM) are crucial for reducing melanoma-related deaths. To support the early detection of melanoma, automated melanoma screening systems have been extensively studied and developed. In this article, we present a hyperspectral melanoma screening system and propose a possible melanoma discrimination index derived from the characteristics of the pigment molecules in the skin, both of which have been derived from hyperspectral data (HSD).</p></div></div><div class="section" id="srt571-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>The index expresses the disordered nature of each lesion including variegation in color based on variation in spectral information obtained from each lesion. Performance of the index in discriminating melanomas from other pigmented skin lesions has been studied in five cases of melanoma (41 HSD sets), one case of Spitz nevus (13 HSD sets), 10 cases of seborrheic keratosis (78 HSD sets), three cases of basal cell carcinoma (16 HSD sets), and nine cases of melanocytic nevus (21 HSD sets), obtained from patients and volunteers, all of whom were Japanese.</p></div></div><div class="section" id="srt571-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Performance of the index, which reflects the disordered nature of a lesion, discriminates melanomas with a sensitivity of 90%, a specificity of 84%, and an area under the receiver operating characteristic curve of 0.93, on resubstitution.</p></div></div><div class="section" id="srt571-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>An objective melanoma discrimination index at a molecular pigmentary level, derived from HSD, has been proposed, and its performance evaluated. This index was highly successful in discriminating MM from non-melanoma, although the statistical population was small.</p></div></div>]]></content:encoded><description>BackgroundEarly detection and proper excision of the primary lesions of malignant melanoma (MM) are crucial for reducing melanoma-related deaths. To support the early detection of melanoma, automated melanoma screening systems have been extensively studied and developed. In this article, we present a hyperspectral melanoma screening system and propose a possible melanoma discrimination index derived from the characteristics of the pigment molecules in the skin, both of which have been derived from hyperspectral data (HSD).MethodsThe index expresses the disordered nature of each lesion including variegation in color based on variation in spectral information obtained from each lesion. Performance of the index in discriminating melanomas from other pigmented skin lesions has been studied in five cases of melanoma (41 HSD sets), one case of Spitz nevus (13 HSD sets), 10 cases of seborrheic keratosis (78 HSD sets), three cases of basal cell carcinoma (16 HSD sets), and nine cases of melanocytic nevus (21 HSD sets), obtained from patients and volunteers, all of whom were Japanese.ResultsPerformance of the index, which reflects the disordered nature of a lesion, discriminates melanomas with a sensitivity of 90%, a specificity of 84%, and an area under the receiver operating characteristic curve of 0.93, on resubstitution.ConclusionAn objective melanoma discrimination index at a molecular pigmentary level, derived from HSD, has been proposed, and its performance evaluated. This index was highly successful in discriminating MM from non-melanoma, although the statistical population was small.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00564.x" xmlns="http://purl.org/rss/1.0/"><title>Development and characterization of a human dermal equivalent with physiological mechanical properties</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00564.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Development and characterization of a human dermal equivalent with physiological mechanical properties</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gwenaël Rolin</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Vincent Placet</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Emmanuelle Jacquet</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Hélène Tauzin</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Sophie Robin</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lionel Pazart</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Celine Viennet</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Philippe Saas</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Patrice Muret</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Delphine Binda</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Philippe Humbert</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-08-30T22:48:21.073657-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00564.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00564.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00564.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt564-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background/aims</h3><div class="para"><p>Different models of reconstructed skin are available, either to provide skin wound healing when this process is deficient, or to be used as an <em>in vitro</em> model. Nevertheless, few studies have focused on the mechanical properties of skin equivalent. Indeed, human skin is naturally under tension. Taking into account these features, the purpose of this work was to obtain a cellularized dermal equivalent (CDE), composed of collagen and dermal fibroblasts.</p></div></div><div class="section" id="srt564-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>To counteract the natural retraction of CDE and to maintain it under tension, different biomaterials were tested. Selection criteria were biocompatibility, bioadhesion properties, ability to induce differentiation of fibroblasts into myofibroblasts and mechanical characterization, considering that of skin <em>in vivo</em>. These assays led to the selection of honeycomb of polyester. CDE constructed on this biomaterial was further characterized mechanically using tensile tests.</p></div></div><div class="section" id="srt564-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>The results showed that mechanical features of the obtained dermal equivalent, including myofibroblasts, were similar to skin <em>in vivo</em>.</p></div></div><div class="section" id="srt564-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>The original model of dermal equivalent presented herein may be a useful tool for clinical use and as an <em>in vitro</em> model for toxicological/pharmacological research.</p></div></div>]]></content:encoded><description>Background/aimsDifferent models of reconstructed skin are available, either to provide skin wound healing when this process is deficient, or to be used as an in vitro model. Nevertheless, few studies have focused on the mechanical properties of skin equivalent. Indeed, human skin is naturally under tension. Taking into account these features, the purpose of this work was to obtain a cellularized dermal equivalent (CDE), composed of collagen and dermal fibroblasts.MethodsTo counteract the natural retraction of CDE and to maintain it under tension, different biomaterials were tested. Selection criteria were biocompatibility, bioadhesion properties, ability to induce differentiation of fibroblasts into myofibroblasts and mechanical characterization, considering that of skin in vivo. These assays led to the selection of honeycomb of polyester. CDE constructed on this biomaterial was further characterized mechanically using tensile tests.ResultsThe results showed that mechanical features of the obtained dermal equivalent, including myofibroblasts, were similar to skin in vivo.ConclusionThe original model of dermal equivalent presented herein may be a useful tool for clinical use and as an in vitro model for toxicological/pharmacological research.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00574.x" xmlns="http://purl.org/rss/1.0/"><title>Criteria for diagnosing pemphigus vulgaris and pemphigus foliaceus by reflectance confocal microscopy</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00574.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Criteria for diagnosing pemphigus vulgaris and pemphigus foliaceus by reflectance confocal microscopy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marta Kurzeja</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Adriana Rakowska</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lidia Rudnicka</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Malgorzata Olszewska</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-08-25T10:01:50.292343-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00574.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00574.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00574.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt574-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Pemphigus is an autoimmune, bullous disease affecting the skin and mucous membranes. The aim of the study was to evaluate whether pemphigus vulgaris (PV) and pemphigus foliaceus (PF), may be diagnosed using reflectance confocal microscopy (RCM).</p></div></div><div class="section" id="srt574-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Thirty patients (18 with PV and 12 with PF) were included into the study. In total, 36 PV lesions and 29 PF lesions were examined. Healthy-appearing skin adjacent to skin lesions and not adjacent to skin lesions was also investigated.</p></div></div><div class="section" id="srt574-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Intraepidermal clefts (bullae) with acantholytic cells were observed in 47% of PV lesions and 59% of PF lesions. Multiple dilated blood vessels in the upper dermis were observed using RCM in 61% of PV lesions and in 86% of PF lesions. RCM features of pemphigus also included presence of inflammatory infiltrates, loss of typical honeycomb pattern of the epidermis, and detachment of the outer root sheath in hair follicles. In 20–64% of cases, RCM features, which are characteristic for PV and PF lesions were also observed in the proximity of these lesions within the healthy-appearing skin. Following criteria for RCM diagnosis of pemphigus were developed: (i) acantholytic clefts in RCM of a lesion, (ii) acantholytic clefts in RCM of healthy-appearing skin adjacent to a lesion, (iii) multiple-dilated blood vessels in RCM of a lesion. Fulfillment of two of these three criteria is sufficient to establish a RCM diagnosis of pemphigus. These criteria do not differentiate between PV and PF.</p></div></div><div class="section" id="srt574-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusions</h3><div class="para"><p>RCM is useful for rapid, non-invasive, in-office differential diagnosis of pemphigus. RCM does not replace immunologic and histopathologic examinations, which remain the gold standard for establishing the final diagnosis of PV and PF.</p></div></div>]]></content:encoded><description>BackgroundPemphigus is an autoimmune, bullous disease affecting the skin and mucous membranes. The aim of the study was to evaluate whether pemphigus vulgaris (PV) and pemphigus foliaceus (PF), may be diagnosed using reflectance confocal microscopy (RCM).MethodsThirty patients (18 with PV and 12 with PF) were included into the study. In total, 36 PV lesions and 29 PF lesions were examined. Healthy-appearing skin adjacent to skin lesions and not adjacent to skin lesions was also investigated.ResultsIntraepidermal clefts (bullae) with acantholytic cells were observed in 47% of PV lesions and 59% of PF lesions. Multiple dilated blood vessels in the upper dermis were observed using RCM in 61% of PV lesions and in 86% of PF lesions. RCM features of pemphigus also included presence of inflammatory infiltrates, loss of typical honeycomb pattern of the epidermis, and detachment of the outer root sheath in hair follicles. In 20–64% of cases, RCM features, which are characteristic for PV and PF lesions were also observed in the proximity of these lesions within the healthy-appearing skin. Following criteria for RCM diagnosis of pemphigus were developed: (i) acantholytic clefts in RCM of a lesion, (ii) acantholytic clefts in RCM of healthy-appearing skin adjacent to a lesion, (iii) multiple-dilated blood vessels in RCM of a lesion. Fulfillment of two of these three criteria is sufficient to establish a RCM diagnosis of pemphigus. These criteria do not differentiate between PV and PF.ConclusionsRCM is useful for rapid, non-invasive, in-office differential diagnosis of pemphigus. RCM does not replace immunologic and histopathologic examinations, which remain the gold standard for establishing the final diagnosis of PV and PF.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00568.x" xmlns="http://purl.org/rss/1.0/"><title>A new method for evaluating postacne scarring</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00568.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">A new method for evaluating postacne scarring</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jin Woong Lee</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Beom Joon Kim</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Myeung Nam Kim</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Young-Hwan Choi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kyungrok Kim</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Eenjun Hwang</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-08-25T10:01:39.745952-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00568.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00568.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00568.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Letter to the Editor</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[]]></content:encoded><description/></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00557.x" xmlns="http://purl.org/rss/1.0/"><title>The preliminary study of the relationship between facial movements and wrinkle formation</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00557.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The preliminary study of the relationship between facial movements and wrinkle formation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Tsutomu Fujimura</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mitsuyuki Hotta</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-08-25T10:01:34.187722-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00557.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00557.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00557.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt557-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>As facial wrinkles develop particularly in areas of the skin that are subject to repeated facial movements, the degree of facial movements may be related to the degree of facial wrinkles, although no data have been reported.</p></div></div><div class="section" id="srt557-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Wrinkles were graded on the faces of Japanese female subjects when they made strong voluntary facial movements (eyes closed tightly, raised eyebrows, and frowns) and also when they were at rest using a set of photos (a photo scale) obtained from subjects with different degrees of wrinkles in the static and dynamic states. Scores obtained were compared between the dynamic and static states, and were analyzed in relation to age and to facial region.</p></div></div><div class="section" id="srt557-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>We found that the levels of wrinkles in both states showed a significant positive correlation with age. Further, the distribution of wrinkles in the dynamic state was found to be similar to those in the static states. Finally, the correlations between static and dynamic wrinkles in the same facial sites were higher than those in different facial sites.</p></div></div><div class="section" id="srt557-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Facial movements cause wrinkling in both the dynamic and the static states and also that static wrinkles may work at the kinetic origins of dynamic wrinkles.</p></div></div>]]></content:encoded><description>BackgroundAs facial wrinkles develop particularly in areas of the skin that are subject to repeated facial movements, the degree of facial movements may be related to the degree of facial wrinkles, although no data have been reported.MethodsWrinkles were graded on the faces of Japanese female subjects when they made strong voluntary facial movements (eyes closed tightly, raised eyebrows, and frowns) and also when they were at rest using a set of photos (a photo scale) obtained from subjects with different degrees of wrinkles in the static and dynamic states. Scores obtained were compared between the dynamic and static states, and were analyzed in relation to age and to facial region.ResultsWe found that the levels of wrinkles in both states showed a significant positive correlation with age. Further, the distribution of wrinkles in the dynamic state was found to be similar to those in the static states. Finally, the correlations between static and dynamic wrinkles in the same facial sites were higher than those in different facial sites.ConclusionFacial movements cause wrinkling in both the dynamic and the static states and also that static wrinkles may work at the kinetic origins of dynamic wrinkles.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00559.x" xmlns="http://purl.org/rss/1.0/"><title>Cutaneous resonance running time is decreased in psoriatic lesions</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00559.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Cutaneous resonance running time is decreased in psoriatic lesions</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Chengzhi Lv</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Shunpeng Song</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wenhai Luo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Peter M. Elias</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mao-Qiang Man</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-08-25T01:01:18.657453-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00559.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00559.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00559.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt559-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background/aims</h3><div class="para"><p>Psoriasis is characterized by lower stratum corneum (SC) hydration and dermal inflammation. Both SC hydration and cutaneous inflammation influence cutaneous resonance running time (CRRT). However, the characteristics of CRRT in psoriatic lesions are largely unknown. In the present study, we assessed whether changes in CRRT occur in psoriatic lesions in Chinese.</p></div></div><div class="section" id="srt559-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>A Reviscometer RVM600 and Corneometer CM 825 were used to measure CRRTs and SC hydration, respectively, in psoriatic lesions (psoriasis vulgaris) on the extensor of forearm in 111 subjects (58 men, 53 women), aged 23–80 years (50.42 ± 1.23 years). The contralateral uninvolved sites served as control.</p></div></div><div class="section" id="srt559-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>In comparison with contralateral uninvolved sites, CRRTs in psoriatic lesions were reduced significantly in all directions. There was neither gender nor age difference in the extent of reduction in CRRTs. However, the reduction of CRRTs varied with measurement directions. Positive correlations of SC hydration with CRRTs were found at some directions in uninvolved and involved sites in young men whereas CRRTs in psoriatic lesions were not correlated with SC hydration in either aged or young women. Moreover, CRRT at 0–6 o'clock direction was positively correlated with SC hydration in involved sites of aged men.</p></div></div><div class="section" id="srt559-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Cutaneous resonance running times are decreased in psoriatic lesions. Reduction of CRRTs varies with measurement directions, but not gender or age. Measurement of CRRTs could be another valuable approach to assess the severity of psoriasis and the efficacy of its treatment.</p></div></div>]]></content:encoded><description>Background/aimsPsoriasis is characterized by lower stratum corneum (SC) hydration and dermal inflammation. Both SC hydration and cutaneous inflammation influence cutaneous resonance running time (CRRT). However, the characteristics of CRRT in psoriatic lesions are largely unknown. In the present study, we assessed whether changes in CRRT occur in psoriatic lesions in Chinese.MethodsA Reviscometer RVM600 and Corneometer CM 825 were used to measure CRRTs and SC hydration, respectively, in psoriatic lesions (psoriasis vulgaris) on the extensor of forearm in 111 subjects (58 men, 53 women), aged 23–80 years (50.42 ± 1.23 years). The contralateral uninvolved sites served as control.ResultsIn comparison with contralateral uninvolved sites, CRRTs in psoriatic lesions were reduced significantly in all directions. There was neither gender nor age difference in the extent of reduction in CRRTs. However, the reduction of CRRTs varied with measurement directions. Positive correlations of SC hydration with CRRTs were found at some directions in uninvolved and involved sites in young men whereas CRRTs in psoriatic lesions were not correlated with SC hydration in either aged or young women. Moreover, CRRT at 0–6 o'clock direction was positively correlated with SC hydration in involved sites of aged men.ConclusionCutaneous resonance running times are decreased in psoriatic lesions. Reduction of CRRTs varies with measurement directions, but not gender or age. Measurement of CRRTs could be another valuable approach to assess the severity of psoriasis and the efficacy of its treatment.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00570.x" xmlns="http://purl.org/rss/1.0/"><title>Analysis of human perception of facial skin radiance by means of image histogram parameters of surface and subsurface reflections from the skin</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00570.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Analysis of human perception of facial skin radiance by means of image histogram parameters of surface and subsurface reflections from the skin</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Akira Matsubara</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Zhiwu Liang</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yuji Sato</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Keiji Uchikawa</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-08-25T01:01:15.363015-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00570.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00570.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00570.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt570-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>The appearance of the skin is the result of complicated light–skin interactions involving surface and subsurface reflections. Radiant skin is a complicated attribute but is important for skin beauty. The aim of the present study was to achieve an understanding of the association between human perceptions of skin radiance and image histogram parameters from technically recorded images of surface and subsurface reflections.</p></div></div><div class="section" id="srt570-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Facial images of 45 subjects were evaluated visually by 30 respondents and were also computer analyzed in terms of their image histogram parameters. A partial least squares regression model was created to explain visual perceptions in terms of the image histogram parameters.</p></div></div><div class="section" id="srt570-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Visual perceptions of subsurface reflections can be explained in terms of the mean from the subsurface reflection image histogram, and visual perceptions of surface reflections can be explained in terms of the standard deviation (SD) and skewness from the surface reflection image histogram. Skin radiance can be explained in terms of the mean from the subsurface reflection and the SD from the surface reflection.</p></div></div><div class="section" id="srt570-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>To acquire skin radiance, a surface reflection component that makes the skin look shiny and a subsurface reflection component that is in line with skin fairness are both needed. A balance of these features provides the origin of skin radiance.</p></div></div>]]></content:encoded><description>BackgroundThe appearance of the skin is the result of complicated light–skin interactions involving surface and subsurface reflections. Radiant skin is a complicated attribute but is important for skin beauty. The aim of the present study was to achieve an understanding of the association between human perceptions of skin radiance and image histogram parameters from technically recorded images of surface and subsurface reflections.MethodsFacial images of 45 subjects were evaluated visually by 30 respondents and were also computer analyzed in terms of their image histogram parameters. A partial least squares regression model was created to explain visual perceptions in terms of the image histogram parameters.ResultsVisual perceptions of subsurface reflections can be explained in terms of the mean from the subsurface reflection image histogram, and visual perceptions of surface reflections can be explained in terms of the standard deviation (SD) and skewness from the surface reflection image histogram. Skin radiance can be explained in terms of the mean from the subsurface reflection and the SD from the surface reflection.ConclusionTo acquire skin radiance, a surface reflection component that makes the skin look shiny and a subsurface reflection component that is in line with skin fairness are both needed. A balance of these features provides the origin of skin radiance.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00555.x" xmlns="http://purl.org/rss/1.0/"><title>Assessment of melanocytic skin lesions with a high-definition laser Doppler imaging system</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00555.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Assessment of melanocytic skin lesions with a high-definition laser Doppler imaging system</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Robert E. Hunger</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rocco Della Torre</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Alexandre Serov</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Thomas Hunziker</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-08-24T22:30:29.981997-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00555.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00555.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00555.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt555-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Early detection is a major goal in the management of malignant melanoma. Besides clinical assessment many noninvasive technologies such as dermoscopy, digital dermoscopy and <em>in vivo</em> laser scanner microscopy are used as additional methods. Herein we tested a system to assess lesional perfusion as a tool for early melanoma detection.</p></div></div><div class="section" id="srt555-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Laser Doppler flow (F<span class="smallCaps">lux</span>E<span class="smallCaps">xplorer</span>) and mole analyser (MA) score (F<span class="smallCaps">oto</span>F<span class="smallCaps">inder</span>) were applied to histologically verified melanocytic nevi (33) and malignant melanomas (12).</p></div></div><div class="section" id="srt555-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Mean perfusion and MA scores were significantly increased in melanoma compared to nevi. However, applying an empirically determined threshold of 16% perfusion increase only 42% of the melanomas fulfilled the criterion of malignancy, whereas with the mole analyzer score 82% of the melanomas fulfilled the criterion of malignancy.</p></div></div><div class="section" id="srt555-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Laser Doppler imaging is a highly sensitive technology to assess skin and skin tumor perfusion <em>in vivo</em>. Although mean perfusion is higher in melanomas compared to nevi the high numbers of false negative results hamper the use of this technology for early melanoma detection.</p></div></div>]]></content:encoded><description>BackgroundEarly detection is a major goal in the management of malignant melanoma. Besides clinical assessment many noninvasive technologies such as dermoscopy, digital dermoscopy and in vivo laser scanner microscopy are used as additional methods. Herein we tested a system to assess lesional perfusion as a tool for early melanoma detection.MethodsLaser Doppler flow (FluxExplorer) and mole analyser (MA) score (FotoFinder) were applied to histologically verified melanocytic nevi (33) and malignant melanomas (12).ResultsMean perfusion and MA scores were significantly increased in melanoma compared to nevi. However, applying an empirically determined threshold of 16% perfusion increase only 42% of the melanomas fulfilled the criterion of malignancy, whereas with the mole analyzer score 82% of the melanomas fulfilled the criterion of malignancy.ConclusionLaser Doppler imaging is a highly sensitive technology to assess skin and skin tumor perfusion in vivo. Although mean perfusion is higher in melanomas compared to nevi the high numbers of false negative results hamper the use of this technology for early melanoma detection.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00573.x" xmlns="http://purl.org/rss/1.0/"><title>Hydration measurements of the stratum corneum: comparison between the capacitance method (digital version of the Corneometer CM 825®) and the impedance method (Skicon-200EX®)</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00573.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Hydration measurements of the stratum corneum: comparison between the capacitance method (digital version of the Corneometer CM 825®) and the impedance method (Skicon-200EX®)</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Peter Clarys</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ron Clijsen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jan Taeymans</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">André O. Barel</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-08-24T22:06:01.394846-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00573.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00573.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00573.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt573-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Measurement of stratum corneum (SC) hydration often involves the use of commercial instruments. The aim of this study was to compare and validate two recent instruments: the Corneometer 825<sup>®</sup> (digital probe) and the Skicon-200 EX<sup>®</sup>.</p></div></div><div class="section" id="srt573-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p><em>In vitro</em> calibration was carried out on filter pads using different solvents, measurements over different layers of plastic foils, and evaluation of desorption kinetics. <em>In vivo</em> measurements were carried out on skin sites covering a range of very dry to well-hydrated skin areas.</p></div></div><div class="section" id="srt573-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Conductance measurements are influenced by electrolytes while capacitance measurements are not. Dielectric constant of the solvents influences the values of both instruments (<em>r</em> respectively 0.92 and 0.99). The capacitance method carries information from deeper layers (up to 45 μm) compared with the conductance instrument (up to 15 μm). Desorption experiments show a strong relation between the amount of water and respectively the capacitance and the conductance values. The <em>in vivo</em> experiments revealed a strong relation between the two methods (<em>r</em> = 0.97). Sensitivity of the capacitance method is limited for the highest hydration values.</p></div></div><div class="section" id="srt573-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusions</h3><div class="para"><p>Both instruments allow a certain calibration and both give good estimates of the SC hydration.</p></div></div>]]></content:encoded><description>BackgroundMeasurement of stratum corneum (SC) hydration often involves the use of commercial instruments. The aim of this study was to compare and validate two recent instruments: the Corneometer 825® (digital probe) and the Skicon-200 EX®.MethodsIn vitro calibration was carried out on filter pads using different solvents, measurements over different layers of plastic foils, and evaluation of desorption kinetics. In vivo measurements were carried out on skin sites covering a range of very dry to well-hydrated skin areas.ResultsConductance measurements are influenced by electrolytes while capacitance measurements are not. Dielectric constant of the solvents influences the values of both instruments (r respectively 0.92 and 0.99). The capacitance method carries information from deeper layers (up to 45 μm) compared with the conductance instrument (up to 15 μm). Desorption experiments show a strong relation between the amount of water and respectively the capacitance and the conductance values. The in vivo experiments revealed a strong relation between the two methods (r = 0.97). Sensitivity of the capacitance method is limited for the highest hydration values.ConclusionsBoth instruments allow a certain calibration and both give good estimates of the SC hydration.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00566.x" xmlns="http://purl.org/rss/1.0/"><title>Two-dimensional dielectric imaging for dermatologic screening: a feasibility study</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00566.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Two-dimensional dielectric imaging for dermatologic screening: a feasibility study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mohammad Habibi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Edit B. Olasz</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">David P. Klemer</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-08-21T22:21:24.550193-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00566.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00566.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00566.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt566-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background/purpose</h3><div class="para"><p>The diagnosis of skin neoplasia can be very challenging, given the low sensitivity and specificity of traditional methods of diagnosis which are based on visual appearance. Techniques which are based on the dielectric properties of cells can improve the diagnostic accuracy of screening techniques; as an example, point-contact coaxial probes for dielectric measurement can improve diagnostic accuracy. Unfortunately, these probes are not well suited for two-dimensional spatial imaging of the skin surface, given that they must be manually scanned over the skin surface.</p></div></div><div class="section" id="srt566-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods/Results</h3><div class="para"><p>An electronic scanning probe was developed and fabricated to simulate an open-ended coaxial probe suitable for two-dimensional dielectric imaging of human skin in real time. A clinical study was undertaken to demonstrate proof-of-concept for the instrumentation. A select group of normal healthy subjects as well as a subject with diagnosed squamous cell carcinoma participated in this study. The electronic scanning probe was found to be a potentially useful tool for providing two-dimensional images from diseased skin.</p></div></div><div class="section" id="srt566-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>The electronic scanning probe used for the present study addresses existing limitations with current coaxial probes. Measurements of healthy and diseased areas of skin are provided to illustrate the feasibility of the approach.</p></div></div>]]></content:encoded><description>Background/purposeThe diagnosis of skin neoplasia can be very challenging, given the low sensitivity and specificity of traditional methods of diagnosis which are based on visual appearance. Techniques which are based on the dielectric properties of cells can improve the diagnostic accuracy of screening techniques; as an example, point-contact coaxial probes for dielectric measurement can improve diagnostic accuracy. Unfortunately, these probes are not well suited for two-dimensional spatial imaging of the skin surface, given that they must be manually scanned over the skin surface.Methods/ResultsAn electronic scanning probe was developed and fabricated to simulate an open-ended coaxial probe suitable for two-dimensional dielectric imaging of human skin in real time. A clinical study was undertaken to demonstrate proof-of-concept for the instrumentation. A select group of normal healthy subjects as well as a subject with diagnosed squamous cell carcinoma participated in this study. The electronic scanning probe was found to be a potentially useful tool for providing two-dimensional images from diseased skin.ConclusionThe electronic scanning probe used for the present study addresses existing limitations with current coaxial probes. Measurements of healthy and diseased areas of skin are provided to illustrate the feasibility of the approach.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00562.x" xmlns="http://purl.org/rss/1.0/"><title>Computer-aided pattern classification system for dermoscopy images</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00562.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Computer-aided pattern classification system for dermoscopy images</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Qaisar Abbas</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Emre Celebi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Irene Fondón</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-08-21T22:21:22.061231-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00562.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00562.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00562.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt562-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Computer-aided pattern classification of melanoma and other pigmented skin lesions is one of the most important tasks for clinical diagnosis. To differentiate between benign and malignant lesions, the extraction of color, architectural order, symmetry of pattern and homogeneity (CASH) is a challenging task.</p></div></div><div class="section" id="srt562-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>In this article, a novel pattern classification system (PCS) based on the clinical CASH rule is presented to classify among six classes of patterns. The PCS system consists of the following five steps: transformation to the CIE<i>L</i>*<em>a</em>*<em>b</em>* color space, pre-processing to enhance the tumor region and removal of hairs, tumor-area segmentation, color and texture feature extraction, and finally, classification based on a multiclass support vector machine.</p></div></div><div class="section" id="srt562-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>The PCS system is tested on a total of 180 dermoscopic images. To test the performance of the PCS diagnostic classifier, the area under the receiver operating characteristics curve (AUC) is utilized. The proposed classifier achieved a sensitivity of 91.64%, specificity of 94.14%, and AUC of 0.948.</p></div></div><div class="section" id="srt562-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>The experimental results demonstrate that the proposed pattern classifier is highly accurate and classify between benign and malignant lesions into some extend. The PCS method is fully automatic and can accurately detect different patterns from dermoscopy images using color and texture properties. Additional pattern features can be included to investigate the impact of pattern classification based on the CASH rule.</p></div></div>]]></content:encoded><description>BackgroundComputer-aided pattern classification of melanoma and other pigmented skin lesions is one of the most important tasks for clinical diagnosis. To differentiate between benign and malignant lesions, the extraction of color, architectural order, symmetry of pattern and homogeneity (CASH) is a challenging task.MethodsIn this article, a novel pattern classification system (PCS) based on the clinical CASH rule is presented to classify among six classes of patterns. The PCS system consists of the following five steps: transformation to the CIEL*a*b* color space, pre-processing to enhance the tumor region and removal of hairs, tumor-area segmentation, color and texture feature extraction, and finally, classification based on a multiclass support vector machine.ResultsThe PCS system is tested on a total of 180 dermoscopic images. To test the performance of the PCS diagnostic classifier, the area under the receiver operating characteristics curve (AUC) is utilized. The proposed classifier achieved a sensitivity of 91.64%, specificity of 94.14%, and AUC of 0.948.ConclusionThe experimental results demonstrate that the proposed pattern classifier is highly accurate and classify between benign and malignant lesions into some extend. The PCS method is fully automatic and can accurately detect different patterns from dermoscopy images using color and texture properties. Additional pattern features can be included to investigate the impact of pattern classification based on the CASH rule.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00561.x" xmlns="http://purl.org/rss/1.0/"><title>Effects of adhesive dressings on stratum corneum conductance</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00561.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Effects of adhesive dressings on stratum corneum conductance</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Maurizio Cavallini</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Riccardo Gazzola</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Luca Vaienti</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-08-21T22:21:11.844003-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00561.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00561.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00561.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt561-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background</h3><div class="para"><p>Stratum corneum is a fundamental layer of epidermis. It acts as a barrier, with antimicrobial features, regulating skin permeability and integrity as well. Adhesive dressings and their removal could alter this layer, affecting cutaneous water balance and lipid composition of stratum corneum. These changes could be monitored by measurement of cutaneous hydration.</p></div></div><div class="section" id="srt561-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>Ninety-two patients affected by wounds dressed with adhesive tapes or plasters have been studied. Measurement of skin conductance under tape/plaster and in the surrounding healthy skin, immediately after removal of dressing has been performed. Dressing age, wound localization, and characteristics were also considered.</p></div></div><div class="section" id="srt561-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Adhesive dressings alter significantly stratum corneum conductance. Although healthy skin hydration has significant variations throughout the body, cutaneous conductance under adhesive dressing in different areas displays no significative changes. Moreover, the increase in hydration due to adhesive tapes/plasters showed no association with wound dehiscence.</p></div></div><div class="section" id="srt561-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Discussion</h3><div class="para"><p>Adhesive dressings cause a significative increase in stratum corneum conductance, acting as a barrier to apocrine secretions. Although different hydration levels have been observed in healthy skin throughout the body, no difference exists under adhesive dressing among different regions, suggesting no contraindications in their employment throughout the body.</p></div></div><div class="section" id="srt561-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>Increase in cutaneous hydration showed no correlations with wound dehiscence, thus confirming safety and practicality of these dressings.</p></div></div>]]></content:encoded><description>BackgroundStratum corneum is a fundamental layer of epidermis. It acts as a barrier, with antimicrobial features, regulating skin permeability and integrity as well. Adhesive dressings and their removal could alter this layer, affecting cutaneous water balance and lipid composition of stratum corneum. These changes could be monitored by measurement of cutaneous hydration.MethodsNinety-two patients affected by wounds dressed with adhesive tapes or plasters have been studied. Measurement of skin conductance under tape/plaster and in the surrounding healthy skin, immediately after removal of dressing has been performed. Dressing age, wound localization, and characteristics were also considered.ResultsAdhesive dressings alter significantly stratum corneum conductance. Although healthy skin hydration has significant variations throughout the body, cutaneous conductance under adhesive dressing in different areas displays no significative changes. Moreover, the increase in hydration due to adhesive tapes/plasters showed no association with wound dehiscence.DiscussionAdhesive dressings cause a significative increase in stratum corneum conductance, acting as a barrier to apocrine secretions. Although different hydration levels have been observed in healthy skin throughout the body, no difference exists under adhesive dressing among different regions, suggesting no contraindications in their employment throughout the body.ConclusionIncrease in cutaneous hydration showed no correlations with wound dehiscence, thus confirming safety and practicality of these dressings.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00567.x" xmlns="http://purl.org/rss/1.0/"><title>Involvement of upper cheek sagging in nasolabial fold formation</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00567.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Involvement of upper cheek sagging in nasolabial fold formation</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Tomonobu Ezure</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Satoshi Amano</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-08-18T07:39:36.756969-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00567.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00567.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00567.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt567-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Background:</h3><div class="para"><p>Nasolabial folds are a well-known feature of aging, but the mechanism of their formation remains unclear.</p></div></div><div class="section" id="srt567-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Objectives:</h3><div class="para"><p>To clarify the mechanism of nasolabial fold formation, we established grading criteria for severity and explored the influence of dermal elasticity and subcutaneous adipose mass. We also investigated the involvement of facial morphological changes, such as wrinkling and sagging.</p></div></div><div class="section" id="srt567-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods:</h3><div class="para"><p>Faces of 108 healthy Japanese female volunteers (age range: 20–60) were photographed at the angle of 45°, and a six-grade photograph-based grading scheme for nasolabial fold severity was established and evaluated. In 70 Japanese female volunteers (middle-aged: 30–50), dermal elasticity was measured with a Cutometer MPA 580<sup>®</sup> and subcutaneous adipose layer thickness was measured by ultrasound using a Prosound alpha 5<sup>®</sup>.</p></div></div><div class="section" id="srt567-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results:</h3><div class="para"><p>Nasolabial fold severity was significantly and positively correlated with age in subjects in their twenties to sixties (<em>R</em> = 0.777, <em>P</em> &lt; 0.001). Nasolabial folds were drastically reduced, or disappeared, when the facial position was changed (subjects lay down instead of sitting) to reduce sagging; only 13.8% of subjects showed fixed wrinkles at the positions of the nasolabial folds after the facial position change. Nasolabial fold severity in middle-aged volunteers was significantly and negatively correlated with dermal elasticity parameters, i.e., net elasticity excluding viscoelastic creep (Ur/Ue), overall elasticity including creep and creep recovery (Ua/Uf), ratio of elastic recovery to total deformation (Ur/Uf), and the negative value of the amount of deformation that did not recover to the original state [−Uf−Ua)], all of which were significantly and negatively correlated with age. Subcutaneous adipose layer thickness was significantly and negatively correlated with dermal elasticity parameter Ua/Uf, and also significantly and positively related to nasolabial fold severity (<em>R</em> = 0.285, <em>P</em> &lt; 0.017).</p></div></div><div class="section" id="srt567-sec-0005" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusions:</h3><div class="para"><p>Nasolabial fold severity increases with decreasing dermal elasticity and with increment of the subcutaneous adipose layer. These changes might induce sagging formation in the upper cheek area, promoting fold formation at the border between the inner and outer nasolabial areas.</p></div></div>]]></content:encoded><description>Background:Nasolabial folds are a well-known feature of aging, but the mechanism of their formation remains unclear.Objectives:To clarify the mechanism of nasolabial fold formation, we established grading criteria for severity and explored the influence of dermal elasticity and subcutaneous adipose mass. We also investigated the involvement of facial morphological changes, such as wrinkling and sagging.Methods:Faces of 108 healthy Japanese female volunteers (age range: 20–60) were photographed at the angle of 45°, and a six-grade photograph-based grading scheme for nasolabial fold severity was established and evaluated. In 70 Japanese female volunteers (middle-aged: 30–50), dermal elasticity was measured with a Cutometer MPA 580® and subcutaneous adipose layer thickness was measured by ultrasound using a Prosound alpha 5®.Results:Nasolabial fold severity was significantly and positively correlated with age in subjects in their twenties to sixties (R = 0.777, P &lt; 0.001). Nasolabial folds were drastically reduced, or disappeared, when the facial position was changed (subjects lay down instead of sitting) to reduce sagging; only 13.8% of subjects showed fixed wrinkles at the positions of the nasolabial folds after the facial position change. Nasolabial fold severity in middle-aged volunteers was significantly and negatively correlated with dermal elasticity parameters, i.e., net elasticity excluding viscoelastic creep (Ur/Ue), overall elasticity including creep and creep recovery (Ua/Uf), ratio of elastic recovery to total deformation (Ur/Uf), and the negative value of the amount of deformation that did not recover to the original state [−Uf−Ua)], all of which were significantly and negatively correlated with age. Subcutaneous adipose layer thickness was significantly and negatively correlated with dermal elasticity parameter Ua/Uf, and also significantly and positively related to nasolabial fold severity (R = 0.285, P &lt; 0.017).Conclusions:Nasolabial fold severity increases with decreasing dermal elasticity and with increment of the subcutaneous adipose layer. These changes might induce sagging formation in the upper cheek area, promoting fold formation at the border between the inner and outer nasolabial areas.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00565.x" xmlns="http://purl.org/rss/1.0/"><title>Noninvasive biosensor for cathepsin L in the stratum corneum</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00565.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Noninvasive biosensor for cathepsin L in the stratum corneum</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Masaki Yamaguchi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Akira Date</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Makoto Sasaki</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Teruhiko Makino</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Tadamichi Shimizu</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-08-12T00:51:13.408382-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00565.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00565.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00565.x</prism:url><prism:section xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">Original Article</prism:section><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">n/a</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="section" id="srt565-sec-0001" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Purpose</h3><div class="para"><p>The objective is to propose an on-site testing biosensor of cathepsin L (CatL) activity in the stratum corneum, which can be used for the evaluation of skin conditions noninvasively and easily.</p></div></div><div class="section" id="srt565-sec-0002" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Methods</h3><div class="para"><p>The biosensor comprises of a disposable test strip and a desktop-sized reader (260 × 150 × 290 mm<sup>3</sup>, 1.9 kg), incorporating a charge-coupled device image sensor (CCD) unit to measure the reflectance of the test strip. A novel immuno-chromatographic test strip was proposed for CatL analysis in the stratum corneum. In order to realize the test strip, a colloidal gold technique was selected as the molecular recognition method for the CatL. A human skin sample was collected noninvasively by adhesive tape stripping.</p></div></div><div class="section" id="srt565-sec-0003" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Results</h3><div class="para"><p>Based on optimal assay conditions, the sensitivity of the biosensor was evaluated. It required 10 min from a sample dropping to appear the test line on the test strip. The optical density was proportion to the CatL. Bioanalytical validation indicated that, within the biosensor's detection limit (172.2 μU/mL), its accuracy (<em>R</em><sup>2</sup> = 0.94), and precision (CV = 15%) approach more elaborate laboratory-based analyzers. In addition, the truncated sampling-reporting cycle (&lt;15 min) allows speedy reporting of CatL levels.</p></div></div><div class="section" id="srt565-sec-0004" xmlns="http://www.w3.org/1999/xhtml"><h3 xhtml="http://www.w3.org/1999/xhtml" xmlns="http://purl.org/rss/1.0/">Conclusion</h3><div class="para"><p>It was indicated that this noninvasive and easy-to use biosensor might be a novel tool for the semi-quantitative analysis of CatL in the stratum corneum.</p></div></div>]]></content:encoded><description>PurposeThe objective is to propose an on-site testing biosensor of cathepsin L (CatL) activity in the stratum corneum, which can be used for the evaluation of skin conditions noninvasively and easily.MethodsThe biosensor comprises of a disposable test strip and a desktop-sized reader (260 × 150 × 290 mm3, 1.9 kg), incorporating a charge-coupled device image sensor (CCD) unit to measure the reflectance of the test strip. A novel immuno-chromatographic test strip was proposed for CatL analysis in the stratum corneum. In order to realize the test strip, a colloidal gold technique was selected as the molecular recognition method for the CatL. A human skin sample was collected noninvasively by adhesive tape stripping.ResultsBased on optimal assay conditions, the sensitivity of the biosensor was evaluated. It required 10 min from a sample dropping to appear the test line on the test strip. The optical density was proportion to the CatL. Bioanalytical validation indicated that, within the biosensor's detection limit (172.2 μU/mL), its accuracy (R2 = 0.94), and precision (CV = 15%) approach more elaborate laboratory-based analyzers. In addition, the truncated sampling-reporting cycle (&lt;15 min) allows speedy reporting of CatL levels.ConclusionIt was indicated that this noninvasive and easy-to use biosensor might be a novel tool for the semi-quantitative analysis of CatL in the stratum corneum.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00549.x" xmlns="http://purl.org/rss/1.0/"><title>Impact of collagen crosslinking on the second harmonic generation signal and the fluorescence lifetime of collagen autofluorescence</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00549.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Impact of collagen crosslinking on the second harmonic generation signal and the fluorescence lifetime of collagen autofluorescence</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Vivien Lutz</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Martin Sattler</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Stefan Gallinat</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Horst Wenck</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ralf Poertner</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Frank Fischer</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-05-12T07:46:39.015542-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00549.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00549.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00549.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background/purpose: </b> Collagen is the major structural protein of the skin and its crosslinks are essential for its mechanical stability. In photodamaged skin, a decrease of the mature collagen crosslink histidinohydroxylysino-norleucine was reported. In this study, we investigated the consequences and measurability of the reduced crosslinking.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> In order to determine the consequences of reduced collagen crosslinking, <em>in vitro</em> models of reduced collagen crosslinking were established. The collagen synthesis and structure was analyzed using the signals second harmonic generation (SHG) and the fluorescence lifetime of the collagen autofluorescence by a multiphoton laser scanning microscope.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> Reduced collagen crosslinking results in a posttranscriptionally diminished collagen synthesis, a modified structure of the collagen fibers and fibrils and a higher intensity of the SHG signal. The SHG signal might be influenced by the interspaces of the collagen molecules within one collagen fibril. Because of these findings, it can be speculated that reduced collagen crosslinking changes the interspace of single collagen molecules within the collagen fibril, resulting in an enhanced SHG signal. Alternative explanations are discussed. Furthermore, the fluorescence lifetime was reduced in the <em>in vitro</em> models of reduced collagen crosslinking. In the crosslink sites of the collagen molecules, the main ratio of fluorescence is found. As the fluorescence lifetime is determined not only by the fluorescent molecule itself but also by its microenvironment, the change in the fluorescence lifetime might be explained by reduced crosslinking at the crosslink site.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> A reduction of collagen crosslinking (as seen in photodamaged skin) results in an increase of the SHG signal and a decrease of the fluorescence lifetime <em>in vitro. In vivo</em> measurements of the two parameters might reveal the status of collagen crosslinking and therefore help to identify the status of dermal photodamage or pathogenesis using collagen crosslinking determination.</p></div>]]></content:encoded><description>Background/purpose:  Collagen is the major structural protein of the skin and its crosslinks are essential for its mechanical stability. In photodamaged skin, a decrease of the mature collagen crosslink histidinohydroxylysino-norleucine was reported. In this study, we investigated the consequences and measurability of the reduced crosslinking.Methods:  In order to determine the consequences of reduced collagen crosslinking, in vitro models of reduced collagen crosslinking were established. The collagen synthesis and structure was analyzed using the signals second harmonic generation (SHG) and the fluorescence lifetime of the collagen autofluorescence by a multiphoton laser scanning microscope.Results:  Reduced collagen crosslinking results in a posttranscriptionally diminished collagen synthesis, a modified structure of the collagen fibers and fibrils and a higher intensity of the SHG signal. The SHG signal might be influenced by the interspaces of the collagen molecules within one collagen fibril. Because of these findings, it can be speculated that reduced collagen crosslinking changes the interspace of single collagen molecules within the collagen fibril, resulting in an enhanced SHG signal. Alternative explanations are discussed. Furthermore, the fluorescence lifetime was reduced in the in vitro models of reduced collagen crosslinking. In the crosslink sites of the collagen molecules, the main ratio of fluorescence is found. As the fluorescence lifetime is determined not only by the fluorescent molecule itself but also by its microenvironment, the change in the fluorescence lifetime might be explained by reduced crosslinking at the crosslink site.Conclusion:  A reduction of collagen crosslinking (as seen in photodamaged skin) results in an increase of the SHG signal and a decrease of the fluorescence lifetime in vitro. In vivo measurements of the two parameters might reveal the status of collagen crosslinking and therefore help to identify the status of dermal photodamage or pathogenesis using collagen crosslinking determination.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00547.x" xmlns="http://purl.org/rss/1.0/"><title>Thermography-measured effect of capsaicin, methylprednisolone and mitomycin on the survival of random skin flaps in rats</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00547.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Thermography-measured effect of capsaicin, methylprednisolone and mitomycin on the survival of random skin flaps in rats</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Dražen Shejbal</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Petar Drvis</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Vladimir Bedekovic</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-05-06T02:57:16.770414-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00547.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00547.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00547.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Aims: </b> This study was designed to determine if steroids, capsaicin and mytomicin improved skin flap survival in rats, and it has confirmed that thermography is an effective method to measured skin flap vitality.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> Forty female Wistar rats were randomised into four groups. A standardised full thickness inferiorly based dorsal random-pattern skin flap was raised, and a gelatine sponge was placed before suturing between the flap and its recipient bed, soaked with 0.9 % saline in the control group and with capsaicin, methylprednisolone and mitomycini in the experimental groups. Vitality of the flap and of the survival area was measured by infrared thermography.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> Methylprednisolone statistically significant decrease skin flap necrosis, approximately 56%, when compared with controls (<em>P</em>&lt; 0.05).</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> Corticosteroids applied subcutaneously in a single dose on a gelatine sponge produced a statistically significant improvement of the survival of random skin flaps in rats, whereas capsaicin and mitomycin showed no improvement.</p></div>]]></content:encoded><description>Aims:  This study was designed to determine if steroids, capsaicin and mytomicin improved skin flap survival in rats, and it has confirmed that thermography is an effective method to measured skin flap vitality.Methods:  Forty female Wistar rats were randomised into four groups. A standardised full thickness inferiorly based dorsal random-pattern skin flap was raised, and a gelatine sponge was placed before suturing between the flap and its recipient bed, soaked with 0.9 % saline in the control group and with capsaicin, methylprednisolone and mitomycini in the experimental groups. Vitality of the flap and of the survival area was measured by infrared thermography.Results:  Methylprednisolone statistically significant decrease skin flap necrosis, approximately 56%, when compared with controls (P&lt; 0.05).Conclusion:  Corticosteroids applied subcutaneously in a single dose on a gelatine sponge produced a statistically significant improvement of the survival of random skin flaps in rats, whereas capsaicin and mitomycin showed no improvement.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00548.x" xmlns="http://purl.org/rss/1.0/"><title>Seemingly healthy skin in atopic dermatitis: observations with the use of high-frequency ultrasonography, preliminary study</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00548.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Seemingly healthy skin in atopic dermatitis: observations with the use of high-frequency ultrasonography, preliminary study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Aleksandra Dańczak-Pazdrowska</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Adriana Polańska</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wojciech Silny</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Anna Sadowska</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Agnieszka Osmola-Mańkowska</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Magdalena Czarnecka-Operacz</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ryszard Żaba</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Dorota Jenerowicz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-05-02T21:54:22.420284-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00548.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00548.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00548.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background: </b> Atopic dermatitis (AD) is a chronic, relapsing skin disorder which is strictly determined by the epidermal barrier function. In previous studies, there is conclusive evidence that normal-looking, nonlesional skin presents meaningful barrier function defect and a sub-clinical eczematous skin reaction.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Aim: </b> The authors intended to visualize nonlesional AD skin with the use of high frequency ultrasonography to show that the normal-looking, nonlesional skin may present significant abnormalities in USG examination.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> We have performed analysis with the use of high-frequency 20 MHz skin sonography in the cases of 15 AD patients of the Department of Dermatology, Medical University, Poznań, Poland. The clinical score has been evaluated on the basis of W-AZS index and EASI. The results were presented in the form of ultrasonographic images.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> High frequency ultrasonography revealed an echopoor band within nonlesional skin of six (40%) examined AD patients and in all cases within skin lesions.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> Our results indicate the significant role of skin ultrasonography in the complete clinical evaluation of patients with AD, which may serve as an element in selection of the most appropriate topical treatment. An echopoor band beneath the echo entry within nonlesional skin of some AD patients may reflect subclinical eczematous reaction and the readiness for the development of typical skin lesions. For this purpose, we suggest to name an intact skin in AD as seemingly healthy skin.</p></div>]]></content:encoded><description>Background:  Atopic dermatitis (AD) is a chronic, relapsing skin disorder which is strictly determined by the epidermal barrier function. In previous studies, there is conclusive evidence that normal-looking, nonlesional skin presents meaningful barrier function defect and a sub-clinical eczematous skin reaction.Aim:  The authors intended to visualize nonlesional AD skin with the use of high frequency ultrasonography to show that the normal-looking, nonlesional skin may present significant abnormalities in USG examination.Methods:  We have performed analysis with the use of high-frequency 20 MHz skin sonography in the cases of 15 AD patients of the Department of Dermatology, Medical University, Poznań, Poland. The clinical score has been evaluated on the basis of W-AZS index and EASI. The results were presented in the form of ultrasonographic images.Results:  High frequency ultrasonography revealed an echopoor band within nonlesional skin of six (40%) examined AD patients and in all cases within skin lesions.Conclusion:  Our results indicate the significant role of skin ultrasonography in the complete clinical evaluation of patients with AD, which may serve as an element in selection of the most appropriate topical treatment. An echopoor band beneath the echo entry within nonlesional skin of some AD patients may reflect subclinical eczematous reaction and the readiness for the development of typical skin lesions. For this purpose, we suggest to name an intact skin in AD as seemingly healthy skin.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00550.x" xmlns="http://purl.org/rss/1.0/"><title>Thermography study of skin response due to whole-body cryotherapy</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00550.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Thermography study of skin response due to whole-body cryotherapy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Armand Cholewka</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Agata Stanek</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Aleksander Sieroń</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Zofia Drzazga</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-04-21T02:24:58.556854-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00550.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00550.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00550.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Purpose: </b> Thermography and contact thermometry were used to study the influence of body mass index (BMI) on the lowering of skin temperature caused by whole-body cryotherapy.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> The study was performed using the Thermovision Camera AGEMA Type 470 and A40. The thermograms of the chosen regions of interests were performed before and immediately after whole-body cryotherapy in a research room outside a cryogenic chamber where the temperature was stabilized. As an additional measurement technique during whole-body cryotherapy, contact thermometry was performed using thermocouples Ni–Cr–Ni–Al stacked to the skin surface.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> The results obtained showed differences in the decrease of skin temperature of predetermined body parts. The largest temperature decrease was observed on the lower extremities. Some differences in the thermal response of similar body parts influenced by the extremely low temperature, with regard to the BMI of volunteers, were observed. This was also found in the results of contact thermometry studies. The statistical analysis confirmed the results of thermography and thermometry studies.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> The magnitude of skin temperature decrease due to the extremely low temperature used in whole-body cryotherapy may be connected to a patient's BMI.</p></div>]]></content:encoded><description>Purpose:  Thermography and contact thermometry were used to study the influence of body mass index (BMI) on the lowering of skin temperature caused by whole-body cryotherapy.Methods:  The study was performed using the Thermovision Camera AGEMA Type 470 and A40. The thermograms of the chosen regions of interests were performed before and immediately after whole-body cryotherapy in a research room outside a cryogenic chamber where the temperature was stabilized. As an additional measurement technique during whole-body cryotherapy, contact thermometry was performed using thermocouples Ni–Cr–Ni–Al stacked to the skin surface.Results:  The results obtained showed differences in the decrease of skin temperature of predetermined body parts. The largest temperature decrease was observed on the lower extremities. Some differences in the thermal response of similar body parts influenced by the extremely low temperature, with regard to the BMI of volunteers, were observed. This was also found in the results of contact thermometry studies. The statistical analysis confirmed the results of thermography and thermometry studies.Conclusion:  The magnitude of skin temperature decrease due to the extremely low temperature used in whole-body cryotherapy may be connected to a patient's BMI.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00546.x" xmlns="http://purl.org/rss/1.0/"><title>Tolerance of low-frequency ultrasound sonophoresis: a double-blind randomized study on humans</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00546.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Tolerance of low-frequency ultrasound sonophoresis: a double-blind randomized study on humans</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Annabel Maruani</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Emilie Vierron</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Laurent Machet</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bruno Giraudeau</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jean-Michel Halimi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Alain Boucaud</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-04-20T22:46:57.854844-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00546.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00546.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00546.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background: </b> Sonophoresis [low-frequency ultrasound (US)] has been used in animals and <em>in vitro</em> to investigate enhanced percutaneous absorption of drugs. No study focused on its clinical human tolerance has been published as yet.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> We aimed to assess the bioeffects of low-frequency US <em>in vivo</em> on human skin in a double-blind randomized-controlled study. We applied pulse-mode US at 36 kHz for 5 min in a step procedure of increasing dosage, from 1.57 to 3.50 W/cm<sup>2</sup>, and placebo. The primary outcome was toxic effects of the procedure, defined as a pain score &gt;40 on a 0–100 mm visual analogue scale or necrosis. Erythema (scored from 0 to 3 in severity) was also evaluated. The secondary outcomes were measurements of skin thickness by high-resolution skin imaging, of skin capacitance and temperature.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> We included 34 healthy volunteers. We found no pain score &gt;38 and no skin necrosis with either US or placebo. Erythema was systematically observed immediately after US application, but after 1 day, we observed three cases in the knee group. The most frequent adverse effect was tinnitus. We observed no marked increase in temperature or cutaneous thickness after US or placebo. Cutaneous capacitance increased immediately after both applications.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> Such data demonstrating good tolerance of sonophoresis can be useful before the initiation of a clinical trial of the therapeutic use of low-frequency sonophoresis in humans.</p></div>]]></content:encoded><description>Background:  Sonophoresis [low-frequency ultrasound (US)] has been used in animals and in vitro to investigate enhanced percutaneous absorption of drugs. No study focused on its clinical human tolerance has been published as yet.Methods:  We aimed to assess the bioeffects of low-frequency US in vivo on human skin in a double-blind randomized-controlled study. We applied pulse-mode US at 36 kHz for 5 min in a step procedure of increasing dosage, from 1.57 to 3.50 W/cm2, and placebo. The primary outcome was toxic effects of the procedure, defined as a pain score &gt;40 on a 0–100 mm visual analogue scale or necrosis. Erythema (scored from 0 to 3 in severity) was also evaluated. The secondary outcomes were measurements of skin thickness by high-resolution skin imaging, of skin capacitance and temperature.Results:  We included 34 healthy volunteers. We found no pain score &gt;38 and no skin necrosis with either US or placebo. Erythema was systematically observed immediately after US application, but after 1 day, we observed three cases in the knee group. The most frequent adverse effect was tinnitus. We observed no marked increase in temperature or cutaneous thickness after US or placebo. Cutaneous capacitance increased immediately after both applications.Conclusion:  Such data demonstrating good tolerance of sonophoresis can be useful before the initiation of a clinical trial of the therapeutic use of low-frequency sonophoresis in humans.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00545.x" xmlns="http://purl.org/rss/1.0/"><title>The objective evaluation of the severity of psoriatic scales with desquamation collecting tapes and image analysis</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00545.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The objective evaluation of the severity of psoriatic scales with desquamation collecting tapes and image analysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. H. Kim</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">B. Y. Kim</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. W. Choi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. O. Kim</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. S. Lee</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. C. Park</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">S. W. Youn</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-04-20T22:23:10.041431-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00545.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00545.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00545.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background: </b> Assessment of psoriatic scales is important to determine the severity of psoriasis. However, there are very limited numbers of objective, quantitative and observer-independent tools for measuring the severity of psoriasis.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Objective: </b> To determine whether the bioengineering parameters of the psoriatic scale can be used to assess the severity of psoriasis instead of the psoriatic severity index of scales (PSIs) score.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> Thirty-four patients with psoriasis were included. A representative lesion from each patient was selected and bioengineering parameters were measured using the Corneofix<sup>®</sup>. Simultaneously, the severity of the scales was assessed by the PSIs score using clinical photographs of the lesions. In addition, skin color and elasticity parameters were also measured using the Colorimeter<sup>®</sup>, the Mexameter<sup>®</sup> and the Cutometer<sup>®</sup>.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> Statistical differences in the scale parameters were observed between the PSIs 2 and 3 scores. Among the scale parameters, the percent area and area in μm<sup>2</sup> were negatively correlated with the PSIs score. In addition, the Colorimeter<sup>®</sup><em>a, b</em> parameters and the Cutometer<sup>®</sup> R9 parameters were significantly correlated with the PSIs score.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusions: </b> The results of this study showed that the severity of psoriatic scales could be measured objectively using the Corneofix<sup>®</sup>.</p></div>]]></content:encoded><description>Background:  Assessment of psoriatic scales is important to determine the severity of psoriasis. However, there are very limited numbers of objective, quantitative and observer-independent tools for measuring the severity of psoriasis.Objective:  To determine whether the bioengineering parameters of the psoriatic scale can be used to assess the severity of psoriasis instead of the psoriatic severity index of scales (PSIs) score.Methods:  Thirty-four patients with psoriasis were included. A representative lesion from each patient was selected and bioengineering parameters were measured using the Corneofix®. Simultaneously, the severity of the scales was assessed by the PSIs score using clinical photographs of the lesions. In addition, skin color and elasticity parameters were also measured using the Colorimeter®, the Mexameter® and the Cutometer®.Results:  Statistical differences in the scale parameters were observed between the PSIs 2 and 3 scores. Among the scale parameters, the percent area and area in μm2 were negatively correlated with the PSIs score. In addition, the Colorimeter®a, b parameters and the Cutometer® R9 parameters were significantly correlated with the PSIs score.Conclusions:  The results of this study showed that the severity of psoriatic scales could be measured objectively using the Corneofix®.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00544.x" xmlns="http://purl.org/rss/1.0/"><title>Skin tumor area extraction using an improved dynamic programming approach</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00544.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Skin tumor area extraction using an improved dynamic programming approach</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Qaisar Abbas</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. E. Celebi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Irene Fondón García</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2011-04-20T22:23:03.491673-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00544.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00544.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00544.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">no</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background/purpose: </b> Border (B) description of melanoma and other pigmented skin lesions is one of the most important tasks for the clinical diagnosis of dermoscopy images using the ABCD rule. For an accurate description of the border, there must be an effective skin tumor area extraction (STAE) method. However, this task is complicated due to uneven illumination, artifacts present in the lesions and smooth areas or fuzzy borders of the desired regions.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> In this paper, a novel STAE algorithm based on improved dynamic programming (IDP) is presented. The STAE technique consists of the following four steps: color space transform, pre-processing, rough tumor area detection and refinement of the segmented area. The procedure is performed in the CIE <em>L</em><sup>*</sup><em>a</em><sup>*</sup><em>b</em><sup>*</sup> color space, which is approximately uniform and is therefore related to dermatologist's perception. After pre-processing the skin lesions to reduce artifacts, the DP algorithm is improved by introducing a local cost function, which is based on color and texture weights.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> The STAE method is tested on a total of 100 dermoscopic images. In order to compare the performance of STAE with other state-of-the-art algorithms, various statistical measures based on dermatologist-drawn borders are utilized as a ground truth. The proposed method outperforms the others with a sensitivity of 96.64%, a specificity of 98.14% and an error probability of 5.23%.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> The results demonstrate that this STAE method by IDP is an effective solution when compared with other state-of-the-art segmentation techniques. The proposed method can accurately extract tumor borders in dermoscopy images.</p></div>]]></content:encoded><description>Background/purpose:  Border (B) description of melanoma and other pigmented skin lesions is one of the most important tasks for the clinical diagnosis of dermoscopy images using the ABCD rule. For an accurate description of the border, there must be an effective skin tumor area extraction (STAE) method. However, this task is complicated due to uneven illumination, artifacts present in the lesions and smooth areas or fuzzy borders of the desired regions.Methods:  In this paper, a novel STAE algorithm based on improved dynamic programming (IDP) is presented. The STAE technique consists of the following four steps: color space transform, pre-processing, rough tumor area detection and refinement of the segmented area. The procedure is performed in the CIE L*a*b* color space, which is approximately uniform and is therefore related to dermatologist's perception. After pre-processing the skin lesions to reduce artifacts, the DP algorithm is improved by introducing a local cost function, which is based on color and texture weights.Results:  The STAE method is tested on a total of 100 dermoscopic images. In order to compare the performance of STAE with other state-of-the-art algorithms, various statistical measures based on dermatologist-drawn borders are utilized as a ground truth. The proposed method outperforms the others with a sensitivity of 96.64%, a specificity of 98.14% and an error probability of 5.23%.Conclusion:  The results demonstrate that this STAE method by IDP is an effective solution when compared with other state-of-the-art segmentation techniques. The proposed method can accurately extract tumor borders in dermoscopy images.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00542.x" xmlns="http://purl.org/rss/1.0/"><title>Acne analysis, grading and computational assessment methods: an overview</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00542.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Acne analysis, grading and computational assessment methods: an overview</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Roshaslinie Ramli</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Aamir Saeed Malik</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Ahmad Fadzil Mohamad Hani</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Adawiyah Jamil</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00542.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00542.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00542.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">1</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">14</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Introduction: </b> This paper presents a comprehensive review of acne grading and measurement. Acne is a chronic disorder of the pilosebaceous units, with excess sebum production, follicular epidermal hyperproliferation, inflammation and <em>Propionibacterium acnes</em> activity. Most patients are affected with acne vulgaris, which is the prevalent type of acne. Acne vulgaris consists of comedones (whitehead and blackhead), papules, pustules, nodules and cysts.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Objectives: </b> To review and identify the issues for acne vulgaris grading and computational assessment methods. To determine the future direction for addressing the identified issues.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> There are two main methods of assessment for acne severity grading, namely, lesion counting and comparison of patient with a photographic standard. For the computational assessment method, the emphasis is on computational imaging techniques.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> Current acne grading methods are very time consuming and tedious. Generally, they rely on approximation for counting lesions and hence the assessment is quite subjective, with both inter and intra-observer variability. It is important to accurately assess acne grade to evaluate its severity as this influences treatment selection and assessment of response to therapy. This will further help in better disease management and more efficacious treatment.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> Semi-automated or automated methods based on computational imaging techniques should be devised for acne grade assessment.</p></div>]]></content:encoded><description>Introduction:  This paper presents a comprehensive review of acne grading and measurement. Acne is a chronic disorder of the pilosebaceous units, with excess sebum production, follicular epidermal hyperproliferation, inflammation and Propionibacterium acnes activity. Most patients are affected with acne vulgaris, which is the prevalent type of acne. Acne vulgaris consists of comedones (whitehead and blackhead), papules, pustules, nodules and cysts.Objectives:  To review and identify the issues for acne vulgaris grading and computational assessment methods. To determine the future direction for addressing the identified issues.Methods:  There are two main methods of assessment for acne severity grading, namely, lesion counting and comparison of patient with a photographic standard. For the computational assessment method, the emphasis is on computational imaging techniques.Results:  Current acne grading methods are very time consuming and tedious. Generally, they rely on approximation for counting lesions and hence the assessment is quite subjective, with both inter and intra-observer variability. It is important to accurately assess acne grade to evaluate its severity as this influences treatment selection and assessment of response to therapy. This will further help in better disease management and more efficacious treatment.Conclusion:  Semi-automated or automated methods based on computational imaging techniques should be devised for acne grade assessment.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00540.x" xmlns="http://purl.org/rss/1.0/"><title>Characterization of a new acne vulgaris treatment device combining light and thermal treatment methods</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00540.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Characterization of a new acne vulgaris treatment device combining light and thermal treatment methods</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yeail Joo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Heesung Kang</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Eung Ho Choi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Stuart Nelson</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Byungjo Jung</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00540.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00540.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00540.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">15</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">21</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background/purpose: </b> Conventional treatment methods for acne vulgaris have various side effects such as the development of bacterial resistance, phototoxicity, vertigo, gastro-intestinal problems, and drug eruptions. To minimize such side effects, light and thermal methods have been alternately suggested. This study characterized a new acne vulgaris treatment device (AVTD) that combines both light and thermal methods and evaluated its clinical efficacy.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> We characterized the thermal and light properties of the AVTD itself and evaluated its thermal characteristics in <em>ex vivo</em> porcine skin samples. The Arrhenius equation was used to calculate the skin thermal injury coefficient to confirm the skin safety of the AVTD. Finally, the clinical efficacy of the AVDT was evaluated by analyzing cross-polarization and erythema index images, which were obtained from 13 volunteers undergoing treatment with the AVTD.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> The temperature of the AVTD itself was maintained at 49.1 °C on the tip and 39.7 °C in the porcine skin samples. The peak intensity of the light-emitting diode (LED) light was observed at 468 nm. The skin safety of the AVTD was confirmed and 84.2% of the volunteers presented positive treatment results.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> The treatment of acne using the AVTD resulted in a high treatment rate in a clinical study, minimizing side effects. On the basis of these results, we can be sure that the AVTD may be effectively used for the treatment of acne vulgaris.</p></div>]]></content:encoded><description>Background/purpose:  Conventional treatment methods for acne vulgaris have various side effects such as the development of bacterial resistance, phototoxicity, vertigo, gastro-intestinal problems, and drug eruptions. To minimize such side effects, light and thermal methods have been alternately suggested. This study characterized a new acne vulgaris treatment device (AVTD) that combines both light and thermal methods and evaluated its clinical efficacy.Methods:  We characterized the thermal and light properties of the AVTD itself and evaluated its thermal characteristics in ex vivo porcine skin samples. The Arrhenius equation was used to calculate the skin thermal injury coefficient to confirm the skin safety of the AVTD. Finally, the clinical efficacy of the AVDT was evaluated by analyzing cross-polarization and erythema index images, which were obtained from 13 volunteers undergoing treatment with the AVTD.Results:  The temperature of the AVTD itself was maintained at 49.1 °C on the tip and 39.7 °C in the porcine skin samples. The peak intensity of the light-emitting diode (LED) light was observed at 468 nm. The skin safety of the AVTD was confirmed and 84.2% of the volunteers presented positive treatment results.Conclusion:  The treatment of acne using the AVTD resulted in a high treatment rate in a clinical study, minimizing side effects. On the basis of these results, we can be sure that the AVTD may be effectively used for the treatment of acne vulgaris.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00536.x" xmlns="http://purl.org/rss/1.0/"><title>Sun-induced changes of stratum corneum hydration vary with age and gender in a normal Chinese population</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00536.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Sun-induced changes of stratum corneum hydration vary with age and gender in a normal Chinese population</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Zhili Liu</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Shunpeng Song</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wenhai Luo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Peter M. Elias</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Mao-Qiang Man</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00536.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00536.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00536.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">22</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">28</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background/objectives: </b> Previous studies have demonstrated that sun-induced alteration of epidermal permeability barrier function varies with gender and age. In the present study, we assess the stratum corneum (SC) hydration in sun-exposed males and females.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> A total of 168 subjects (84 males and 84 females) aged 19–75 years were enrolled. A multifunctional skin physiology monitor was used to measure SC hydration.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> In comparison with non-sun exposure, sun exposure does not cause a significant change in SC hydration in either young males or young females, whereas in aged females, a significant reduction of SC hydration is seen on the forehead and the dorsal hand of sun-exposed subjects. SC hydration on the canthus of both aged males and aged females is significantly lower than that of young subjects. Additionally, SC hydration on the dorsal hand of aged females is also significantly lower as compared with young females. Sun-induced reduction of SC hydration is more evident on the dorsal hand of aged females than that of males (<em>P</em>&lt;0.001). Moreover, the SC rehydration capacity is significantly lower in sun-exposed aged females than in age-matched males.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> These results demonstrated that sun-induced changes of the SC hydration property vary with age and gender.</p></div>]]></content:encoded><description>Background/objectives:  Previous studies have demonstrated that sun-induced alteration of epidermal permeability barrier function varies with gender and age. In the present study, we assess the stratum corneum (SC) hydration in sun-exposed males and females.Methods:  A total of 168 subjects (84 males and 84 females) aged 19–75 years were enrolled. A multifunctional skin physiology monitor was used to measure SC hydration.Results:  In comparison with non-sun exposure, sun exposure does not cause a significant change in SC hydration in either young males or young females, whereas in aged females, a significant reduction of SC hydration is seen on the forehead and the dorsal hand of sun-exposed subjects. SC hydration on the canthus of both aged males and aged females is significantly lower than that of young subjects. Additionally, SC hydration on the dorsal hand of aged females is also significantly lower as compared with young females. Sun-induced reduction of SC hydration is more evident on the dorsal hand of aged females than that of males (P&lt;0.001). Moreover, the SC rehydration capacity is significantly lower in sun-exposed aged females than in age-matched males.Conclusion:  These results demonstrated that sun-induced changes of the SC hydration property vary with age and gender.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00537.x" xmlns="http://purl.org/rss/1.0/"><title>Differences in the surface and subsurface reflection characteristics of facial skin by age group</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00537.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Differences in the surface and subsurface reflection characteristics of facial skin by age group</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Akira Matsubara</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00537.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00537.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00537.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">29</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">35</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background/purpose: </b> The age-dependent changes of facial skin imperfections such as spot or wrinkles have been investigated repeatedly by means of various objective measurements. However, the age-dependent changes in the optical-reflection characteristics that create a perception of a shine or a glow of the skin have received little attention. We evaluated the age dependence of the optical-reflection characteristics of the surface and subsurface facial skin layers of three age groups.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methodology: </b> The facial skin of 83 Japanese females ranging in age from 20 to 49 years was examined using a high-resolution digital camera equipped with a linear polarizing filter under polarized illumination. Surface and subsurface reflection components were extracted by means of an image-processing technique. In addition to the reflection characteristics, skin hydration, the melanin index, and the hemoglobin index were also measured.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> Significant age-dependent changes were found in the evenness of the surface reflection and in the intensity of the subsurface reflection. In contrast, no difference was observed in the intensity of the surface reflection or in the evenness of the subsurface reflection. The melanin index showed a significant age-dependent difference, with a trend similar to that of the subsurface reflection intensity, but the skin hydration and hemoglobin index showed no difference by age group.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> Surface and subsurface reflection characteristics show age-dependent changes. Younger skin has a greater subsurface reflectivity and a more even surface reflectivity. These optical characteristics of the skin might be related to the perception of consumers that younger skin is brighter and more radiant with an internal glow, whereas aged skin is shinier or glossier.</p></div>]]></content:encoded><description>Background/purpose:  The age-dependent changes of facial skin imperfections such as spot or wrinkles have been investigated repeatedly by means of various objective measurements. However, the age-dependent changes in the optical-reflection characteristics that create a perception of a shine or a glow of the skin have received little attention. We evaluated the age dependence of the optical-reflection characteristics of the surface and subsurface facial skin layers of three age groups.Methodology:  The facial skin of 83 Japanese females ranging in age from 20 to 49 years was examined using a high-resolution digital camera equipped with a linear polarizing filter under polarized illumination. Surface and subsurface reflection components were extracted by means of an image-processing technique. In addition to the reflection characteristics, skin hydration, the melanin index, and the hemoglobin index were also measured.Results:  Significant age-dependent changes were found in the evenness of the surface reflection and in the intensity of the subsurface reflection. In contrast, no difference was observed in the intensity of the surface reflection or in the evenness of the subsurface reflection. The melanin index showed a significant age-dependent difference, with a trend similar to that of the subsurface reflection intensity, but the skin hydration and hemoglobin index showed no difference by age group.Conclusion:  Surface and subsurface reflection characteristics show age-dependent changes. Younger skin has a greater subsurface reflectivity and a more even surface reflectivity. These optical characteristics of the skin might be related to the perception of consumers that younger skin is brighter and more radiant with an internal glow, whereas aged skin is shinier or glossier.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00511.x" xmlns="http://purl.org/rss/1.0/"><title>Classification of Papulo-Squamous skin diseases using image analysis</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00511.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Classification of Papulo-Squamous skin diseases using image analysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. M. Mashaly</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">N. A. Masood</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Abdalla S. A. Mohamed</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00511.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00511.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00511.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">36</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">44</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Introduction: </b> Papulo-squamous skin diseases are variable but are very close in their clinical features. They present with the same lesions, erythematous scaly lesions. Clinical evaluation of skin lesions is based on common sense and experience of the dermatologist to differentiate features of each disease.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Aim: </b> To evaluate a computer-based image analysis system as a helping tool for classification of commonly encountered diseases.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Materials and Methods: </b> The study included 50 selected images from each of psoriasis, lichen planus, atopic dermatitis, seborrheic dermatitis, pityrasis rosea, and pitryasis rubra pilaris with a total of 300 images. The study comprised three main processes peformed on the 300 included images: segmentation, feature extraction followed by classification.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> Rough sets recorded the highest percentage of accuracy and sensitivity of segmentation for the six groups of diseases compared with the other three used techniques (topological derivative, K-means clustering, and watershed). Rule-based classifier using the concept of rough sets recorded the best percentage of classification (96.7%) for the six groups of diseases compared with the other six techniques of classification used: K-means clustering, fuzzy c-means clustering, classification and regression tree, rule-based classifier with discretization, and K-nearest neighbor technique.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> Rough sets approach proves its superiority for both the segmentation and the classification processes of papulo-squamous skin diseases compared with the other used segmentation and classification techniques.</p></div>]]></content:encoded><description>Introduction:  Papulo-squamous skin diseases are variable but are very close in their clinical features. They present with the same lesions, erythematous scaly lesions. Clinical evaluation of skin lesions is based on common sense and experience of the dermatologist to differentiate features of each disease.Aim:  To evaluate a computer-based image analysis system as a helping tool for classification of commonly encountered diseases.Materials and Methods:  The study included 50 selected images from each of psoriasis, lichen planus, atopic dermatitis, seborrheic dermatitis, pityrasis rosea, and pitryasis rubra pilaris with a total of 300 images. The study comprised three main processes peformed on the 300 included images: segmentation, feature extraction followed by classification.Results:  Rough sets recorded the highest percentage of accuracy and sensitivity of segmentation for the six groups of diseases compared with the other three used techniques (topological derivative, K-means clustering, and watershed). Rule-based classifier using the concept of rough sets recorded the best percentage of classification (96.7%) for the six groups of diseases compared with the other six techniques of classification used: K-means clustering, fuzzy c-means clustering, classification and regression tree, rule-based classifier with discretization, and K-nearest neighbor technique.Conclusion:  Rough sets approach proves its superiority for both the segmentation and the classification processes of papulo-squamous skin diseases compared with the other used segmentation and classification techniques.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00529.x" xmlns="http://purl.org/rss/1.0/"><title>Preliminary evaluation of particle systems visualization on the skin surface by scanning electron microscopy and transparency profilometry</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00529.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Preliminary evaluation of particle systems visualization on the skin surface by scanning electron microscopy and transparency profilometry</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Paola Perugini</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Vettor</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Bleve</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G. Bruni</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Mondelli</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">G. F. Secchi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">F. Pavanetto</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00529.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00529.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00529.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">45</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">54</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background: </b> There is a rising debate concerning the possible side effects arising from the use of particles at nanosize since the production of nanomaterials is increasing worldwide. Nanoparticles are able to enter the body through the skin, lungs or intestinal tract, depositing in several organs, and the risk associated with exposure to them, the routes of entry and the molecular mechanisms of any cytotoxicity need to be well understood. The aim of this work was to evaluate the suitability of skin replica as a method to study the colloidal systems visualization and distribution on skin surface.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> Solid lipid nanoparticles (SLN) were used as carrier systems. Skin replicas on healthy volunteers, before and after SLN application, were prepared and visualized using profilometry and scanning electron microscopy (SEM).</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> The results obtained in our study show that skin replica represents a suitable method to study the colloidal systems and their interaction with the skin surface.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> Profilometry enabled us to observe the systems distribution on a cutaneous texture. In addition, SEM, thanks to its high magnifications and field depth, allowed us to evaluate particles' distribution on the skin texture and the interaction between particles of different compositions and replica silicone.</p></div>]]></content:encoded><description>Background:  There is a rising debate concerning the possible side effects arising from the use of particles at nanosize since the production of nanomaterials is increasing worldwide. Nanoparticles are able to enter the body through the skin, lungs or intestinal tract, depositing in several organs, and the risk associated with exposure to them, the routes of entry and the molecular mechanisms of any cytotoxicity need to be well understood. The aim of this work was to evaluate the suitability of skin replica as a method to study the colloidal systems visualization and distribution on skin surface.Methods:  Solid lipid nanoparticles (SLN) were used as carrier systems. Skin replicas on healthy volunteers, before and after SLN application, were prepared and visualized using profilometry and scanning electron microscopy (SEM).Results:  The results obtained in our study show that skin replica represents a suitable method to study the colloidal systems and their interaction with the skin surface.Conclusion:  Profilometry enabled us to observe the systems distribution on a cutaneous texture. In addition, SEM, thanks to its high magnifications and field depth, allowed us to evaluate particles' distribution on the skin texture and the interaction between particles of different compositions and replica silicone.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00530.x" xmlns="http://purl.org/rss/1.0/"><title>The influence of stratum corneum hydration on body fat determination by bioelectrical impedance analysis</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00530.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The influence of stratum corneum hydration on body fat determination by bioelectrical impedance analysis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Peter Clarys</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">P. Deriemaeker</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. Clijsen</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Taeymans</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">D. Aerenhouts</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. O. Barel</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00530.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00530.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00530.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">55</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">60</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background/aims: </b> Bioelectrical impedance analysis (BIA) is used for the estimation of the amount of body fat. We evaluated the influence of the stratum corneum hydration at the contact areas used for BIA on the body fat estimation.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> Stratum corneum hydration was measured at the sole of the right foot and the palm of the right hand before and after contact with the Tanita Body Composition Analyzer TBF 410<sup>®</sup> and the Omron Body Fat Analyzer<sup>®</sup>, (<em>n</em>=128 females and 126 males), respectively. Changes in stratum corneum hydration during the contact time were calculated (ΔHYD). As a gold standard for body fat estimation, the underwater weighing method (UWW) was used and the deviation of this standard was calculated for the Tanita (DT) and the Omron (DO) measurement.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> During contact with the Tanita, stratum corneum hydration increased significantly at the foot. Neither stratum corneum hydration measured at the respective contact sites before BIA nor ΔHYD at the respective skin sites was related to DT or with DO.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> The BIA measuring procedure using the Tanita instrument leads to an occlusive effect at the contact site. BIA for the determination of body composition is not influenced by stratum corneum hydration.</p></div>]]></content:encoded><description>Background/aims:  Bioelectrical impedance analysis (BIA) is used for the estimation of the amount of body fat. We evaluated the influence of the stratum corneum hydration at the contact areas used for BIA on the body fat estimation.Methods:  Stratum corneum hydration was measured at the sole of the right foot and the palm of the right hand before and after contact with the Tanita Body Composition Analyzer TBF 410® and the Omron Body Fat Analyzer®, (n=128 females and 126 males), respectively. Changes in stratum corneum hydration during the contact time were calculated (ΔHYD). As a gold standard for body fat estimation, the underwater weighing method (UWW) was used and the deviation of this standard was calculated for the Tanita (DT) and the Omron (DO) measurement.Results:  During contact with the Tanita, stratum corneum hydration increased significantly at the foot. Neither stratum corneum hydration measured at the respective contact sites before BIA nor ΔHYD at the respective skin sites was related to DT or with DO.Conclusion:  The BIA measuring procedure using the Tanita instrument leads to an occlusive effect at the contact site. BIA for the determination of body composition is not influenced by stratum corneum hydration.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00531.x" xmlns="http://purl.org/rss/1.0/"><title>Evaluation of allergic vesicular reaction to patch test using in vivo confocal microscopy</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00531.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Evaluation of allergic vesicular reaction to patch test using in vivo confocal microscopy</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Marco Ardigò</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Caterina Longo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Antonio Cristaudo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Enzo Berardesca</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Giovanni Pellacani</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00531.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00531.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00531.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">61</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">63</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background: </b> Confocal microscopy has been successfully applied both in oncologic and inflammatory diseases. In particular, it has been proved as a useful tool for the <em>in vivo</em> detection of microscopical changes occurring in allergic reactions.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Aims of the study: </b> To evaluate microscopic changes occurring in positive patch test reactions.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> Eight patients with history of allergic dermatitis and positive patch test reaction were analysed by means of confocal microscopy.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> Confocal microscopy showed the presence of spongiotic vesicle preferentially localized around the adnexal ducts that appeared to be in the middle of the spongiotic phenomena.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> Confocal microscopy offered for the first time new insight into vesicle formation and development, showing that adnexal ducts can play a role in allergic reaction.</p></div>]]></content:encoded><description>Background:  Confocal microscopy has been successfully applied both in oncologic and inflammatory diseases. In particular, it has been proved as a useful tool for the in vivo detection of microscopical changes occurring in allergic reactions.Aims of the study:  To evaluate microscopic changes occurring in positive patch test reactions.Methods:  Eight patients with history of allergic dermatitis and positive patch test reaction were analysed by means of confocal microscopy.Results:  Confocal microscopy showed the presence of spongiotic vesicle preferentially localized around the adnexal ducts that appeared to be in the middle of the spongiotic phenomena.Conclusion:  Confocal microscopy offered for the first time new insight into vesicle formation and development, showing that adnexal ducts can play a role in allergic reaction.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00532.x" xmlns="http://purl.org/rss/1.0/"><title>Patterns of aluminum hydroxychloride deposition onto the skin</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00532.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Patterns of aluminum hydroxychloride deposition onto the skin</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Géraldine Mayeux</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Emmanuelle Xhauflaire-Uhoda</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Gérald E. Piérard</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00532.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00532.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00532.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">64</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">69</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background: </b> Aluminum hydroxychloride (AlCl<sub>3</sub>) is an antiperspirant.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Aim: </b> To revisit the AlCl<sub>3</sub> deposition <em>in vivo</em> and <em>in vitro</em> on glass slides and stratum corneum (SC) harvested by cyanoacrylate skin surface strippings (CSSS).</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> Transepidermal water loss (TEWL) was assessed following application of 5% AlCl<sub>3</sub> on the forearms. The AlCl<sub>3</sub>-coated skin, glass slides and CSSS were observed using two ultraviolet light-emitting CCD cameras in order to record changes in specular reflectance related to AlCl<sub>3</sub> deposition. In addition, the corneoxenometry bioassay was performed in order to predict AlCl<sub>3</sub> irritation.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> AlCl<sub>3</sub> deposited on glass slides looked as linear threads and rings of similar sizes. AlCl<sub>3</sub> deposits on skin were almost restricted inside the microrelief lines and as annular deposits at their crossings where acrosyringia are opening. After daily AlCl<sub>3</sub> applications, deposits extended on the CSSS plateaus. At rest in absence of sweating, TEWL was decreased following AlCl<sub>3</sub> applications. During physical exercise, the TEWL increase was limited on the AlCl<sub>3</sub> areas. CSSS appeared unreactive to AlCl<sub>3</sub> at the corneoxenometry bioassay.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> The similar aspect of AlCl<sub>3</sub> deposits on human SC and on glass slides suggested a physical property of AlCl<sub>3</sub>. Repetitive applications of AlCl<sub>3</sub> increased both the deposit area and the barrier function.</p></div>]]></content:encoded><description>Background:  Aluminum hydroxychloride (AlCl3) is an antiperspirant.Aim:  To revisit the AlCl3 deposition in vivo and in vitro on glass slides and stratum corneum (SC) harvested by cyanoacrylate skin surface strippings (CSSS).Methods:  Transepidermal water loss (TEWL) was assessed following application of 5% AlCl3 on the forearms. The AlCl3-coated skin, glass slides and CSSS were observed using two ultraviolet light-emitting CCD cameras in order to record changes in specular reflectance related to AlCl3 deposition. In addition, the corneoxenometry bioassay was performed in order to predict AlCl3 irritation.Results:  AlCl3 deposited on glass slides looked as linear threads and rings of similar sizes. AlCl3 deposits on skin were almost restricted inside the microrelief lines and as annular deposits at their crossings where acrosyringia are opening. After daily AlCl3 applications, deposits extended on the CSSS plateaus. At rest in absence of sweating, TEWL was decreased following AlCl3 applications. During physical exercise, the TEWL increase was limited on the AlCl3 areas. CSSS appeared unreactive to AlCl3 at the corneoxenometry bioassay.Conclusion:  The similar aspect of AlCl3 deposits on human SC and on glass slides suggested a physical property of AlCl3. Repetitive applications of AlCl3 increased both the deposit area and the barrier function.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00533.x" xmlns="http://purl.org/rss/1.0/"><title>Novel anti-wrinkle effect of cosmeceutical product with new retinyl retinoate microsphere using biodegradable polymer</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00533.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Novel anti-wrinkle effect of cosmeceutical product with new retinyl retinoate microsphere using biodegradable polymer</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. Kim</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Kim</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Y. Quan</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">T. Moon</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Mun</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. Cho</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">N. Park</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">W. Moon</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. Lee</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. Kim</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">J. Lee</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. Ryoo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. Jung</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00533.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00533.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00533.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">70</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">76</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background: </b> The novel hybrid retinoid, retinyl retinoate, is a synthetic material that was designed to reduce the side effects of retinoic acid and to increase the stability of retinol. The formulation of the retinyl retinoate, however, is required to enhance skin permeation, and thus to increase the anti-wrinkle effect.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Aim: </b> To identify the efficacy of retinyl retinoate microsphere using biodegradable polymer as an anti-aging agent of cosmetics in treating females over 30 years old with periorbital wrinkles.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> The retinyl retinoate microsphere was prepared using the biodegradable polymer; polylactic acid (PLA). We also conducted two clinical studies with a total of 44 Korean women for 12 weeks. In the first clinical study, 20 patients completed a 12-week trial of cream A [3% PLA-retinyl retinoate (2%) microsphere] applied twice daily to the face. In the second clinical study, 24 patients completed a 12-week trial of cream B (0.06% retinyl retinoate) applied twice daily to the face. Efficacy was based on a global photodamage score, photographs, and image analysis using replicas and Visiometers every 4 weeks.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> The PLA-retinyl retinoate microsphere was more effective for the permeation of retinyl retinoate than retinyl retinoate in itself. The cream A, which contains 3% PLA-retinyl retinoate (2%) microsphere, showed a statistically significant improvement in facial wrinkles (<em>P</em>&lt;0.05) in 20 volunteers after only 4 weeks of application in a clinical trial test. The visual wrinkle improvement and the maximum roughness improvement rate (R2) for cream A was 6.05%, 8.03% higher than that of cream B which contains 0.06% retinyl retinoate, after 4 weeks.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> Retinyl retinoate has a potent anti-wrinkle activity, and the PLA-retinyl retinoate microsphere could be a useful cosmeceutical product for anti-aging purposes.</p></div>]]></content:encoded><description>Background:  The novel hybrid retinoid, retinyl retinoate, is a synthetic material that was designed to reduce the side effects of retinoic acid and to increase the stability of retinol. The formulation of the retinyl retinoate, however, is required to enhance skin permeation, and thus to increase the anti-wrinkle effect.Aim:  To identify the efficacy of retinyl retinoate microsphere using biodegradable polymer as an anti-aging agent of cosmetics in treating females over 30 years old with periorbital wrinkles.Methods:  The retinyl retinoate microsphere was prepared using the biodegradable polymer; polylactic acid (PLA). We also conducted two clinical studies with a total of 44 Korean women for 12 weeks. In the first clinical study, 20 patients completed a 12-week trial of cream A [3% PLA-retinyl retinoate (2%) microsphere] applied twice daily to the face. In the second clinical study, 24 patients completed a 12-week trial of cream B (0.06% retinyl retinoate) applied twice daily to the face. Efficacy was based on a global photodamage score, photographs, and image analysis using replicas and Visiometers every 4 weeks.Results:  The PLA-retinyl retinoate microsphere was more effective for the permeation of retinyl retinoate than retinyl retinoate in itself. The cream A, which contains 3% PLA-retinyl retinoate (2%) microsphere, showed a statistically significant improvement in facial wrinkles (P&lt;0.05) in 20 volunteers after only 4 weeks of application in a clinical trial test. The visual wrinkle improvement and the maximum roughness improvement rate (R2) for cream A was 6.05%, 8.03% higher than that of cream B which contains 0.06% retinyl retinoate, after 4 weeks.Conclusion:  Retinyl retinoate has a potent anti-wrinkle activity, and the PLA-retinyl retinoate microsphere could be a useful cosmeceutical product for anti-aging purposes.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00534.x" xmlns="http://purl.org/rss/1.0/"><title>Unsupervised sub-segmentation for pigmented skin lesions</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00534.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Unsupervised sub-segmentation for pigmented skin lesions</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Zhao Liu</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jiuai Sun</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Melvyn Smith</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Lyndon Smith</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Robert Warr</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00534.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00534.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00534.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">77</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">87</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background: </b> Early identification of malignant melanoma with the surgical removal of thin lesions is the most effective treatment for skin cancers. A computer-aided diagnostic system assists to improve the diagnostic accuracy, where segmenting lesion from normal skin is usually considered as the first step. One of the challenges in the automated segmentation of skin lesions arises from the fact that darker areas within the lesion should be considered separate from the more general suspicious lesion as a whole, because these pigmented areas can provide significant additional diagnostic information.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> This paper presents, for the first time, an unsupervised segmentation scheme to allow the isolation of normal skin, pigmented skin lesions, and interesting darker areas inside the lesion simultaneously. An adaptive mean-shift is first applied with a 5D spatial colour–texture feature space to generate a group of homogenous regions. Then the sub-segmentation maps are calculated by integrating maximal similarity-based region merging and the kernel <em>k</em>-means algorithm, where the number of segments is defined by a cluster validity measurement.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> The proposed method has been validated extensively on both normal digital photographs and dermoscopy images, which demonstrates competitive performance in achieving automatic segmentation. The isolated dark areas have proved helpful in the discrimination of malignant melanomas from atypical benign nevi. Compared with the results obtained from the asymmetry measure of the entire lesion, the asymmetry distribution of the isolated dark areas helped increase the accuracy of the identification of malignant melanoma from 65.38% to 73.07%, and this classification accuracy reached 80.77% on integrating both asymmetry descriptors.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> The proposed segmentation scheme gives the lesion boundary closed to the manual segmentation obtained by experienced dermatologists. The initial classification results indicate that the study of the distributions of darker areas inside the lesions is very promising in characterizing melanomas.</p></div>]]></content:encoded><description>Background:  Early identification of malignant melanoma with the surgical removal of thin lesions is the most effective treatment for skin cancers. A computer-aided diagnostic system assists to improve the diagnostic accuracy, where segmenting lesion from normal skin is usually considered as the first step. One of the challenges in the automated segmentation of skin lesions arises from the fact that darker areas within the lesion should be considered separate from the more general suspicious lesion as a whole, because these pigmented areas can provide significant additional diagnostic information.Methods:  This paper presents, for the first time, an unsupervised segmentation scheme to allow the isolation of normal skin, pigmented skin lesions, and interesting darker areas inside the lesion simultaneously. An adaptive mean-shift is first applied with a 5D spatial colour–texture feature space to generate a group of homogenous regions. Then the sub-segmentation maps are calculated by integrating maximal similarity-based region merging and the kernel k-means algorithm, where the number of segments is defined by a cluster validity measurement.Results:  The proposed method has been validated extensively on both normal digital photographs and dermoscopy images, which demonstrates competitive performance in achieving automatic segmentation. The isolated dark areas have proved helpful in the discrimination of malignant melanomas from atypical benign nevi. Compared with the results obtained from the asymmetry measure of the entire lesion, the asymmetry distribution of the isolated dark areas helped increase the accuracy of the identification of malignant melanoma from 65.38% to 73.07%, and this classification accuracy reached 80.77% on integrating both asymmetry descriptors.Conclusion:  The proposed segmentation scheme gives the lesion boundary closed to the manual segmentation obtained by experienced dermatologists. The initial classification results indicate that the study of the distributions of darker areas inside the lesions is very promising in characterizing melanomas.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00535.x" xmlns="http://purl.org/rss/1.0/"><title>Thermography as a predictor of postherpetic neuralgia in acute herpes zoster patients: a preliminary study</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00535.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Thermography as a predictor of postherpetic neuralgia in acute herpes zoster patients: a preliminary study</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Juhee Park</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Woo Sun Jang</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kui Young Park</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Kapsok Li</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Seong Jun Seo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Chang Kwun Hong</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Jong Beum Lee</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00535.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00535.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00535.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">88</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">93</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background/purpose: </b> Infrared thermal images in patients suffering from herpes zoster (HZ) may exhibit thermal asymmetry due to the unilateral distribution of HZ lesions. This study examined the usefulness of infrared thermography in acute HZ as a predictor for the development of postherpetic neuralgia (PHN).</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> The authors collected demographic and clinical data including age, sex, onset of skin lesion, pain intensity by a visual analogue scale (VAS) and the development of PHN from a total of 55 patients diagnosed with HZ. We evaluated the body surface thermographic parameters between the lesion and contralateral normal skin: maximal difference in the temperature (Δ<em>T</em>) and the size of the body surface area (BSA) showing thermal asymmetry.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> Temperatures of the lesions were found to be warmer than the control side in most patients with acute HZ. We compared the patient group who developed PHN with those who did not. In univariate analysis, patients with PHN were older (<em>P</em>=0.004), had a higher VAS score for pain (<em>P</em>&lt;0.001), higher Δ<em>T</em> (<em>P</em>&lt;0.001) and larger BSA (<em>P</em>=0.001). In logistic regression analysis to identify independent risk factors of PHN, older age (&gt;60 years old) and Δ<em>T</em> more than 0.5 °C were found to be statistically significant.</p></div>]]></content:encoded><description>Background/purpose:  Infrared thermal images in patients suffering from herpes zoster (HZ) may exhibit thermal asymmetry due to the unilateral distribution of HZ lesions. This study examined the usefulness of infrared thermography in acute HZ as a predictor for the development of postherpetic neuralgia (PHN).Methods:  The authors collected demographic and clinical data including age, sex, onset of skin lesion, pain intensity by a visual analogue scale (VAS) and the development of PHN from a total of 55 patients diagnosed with HZ. We evaluated the body surface thermographic parameters between the lesion and contralateral normal skin: maximal difference in the temperature (ΔT) and the size of the body surface area (BSA) showing thermal asymmetry.Results:  Temperatures of the lesions were found to be warmer than the control side in most patients with acute HZ. We compared the patient group who developed PHN with those who did not. In univariate analysis, patients with PHN were older (P=0.004), had a higher VAS score for pain (P&lt;0.001), higher ΔT (P&lt;0.001) and larger BSA (P=0.001). In logistic regression analysis to identify independent risk factors of PHN, older age (&gt;60 years old) and ΔT more than 0.5 °C were found to be statistically significant.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00538.x" xmlns="http://purl.org/rss/1.0/"><title>Investigation of the influence of textiles and surface treatments on blistering using a novel simulant</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00538.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Investigation of the influence of textiles and surface treatments on blistering using a novel simulant</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. Guerra</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">C. J. Schwartz</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00538.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00538.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00538.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">94</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">100</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background: </b> Friction blisters occur when shear loading causes the separation of dermal layers. Consequences range from minor pain to life-threatening infection. Past research in blister formation has focused on <em>in vivo</em> experiments, which complicate a mechanics-based study of the phenomenon.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> A Synthetic Skin Simulant Platform (3SP) approach was developed to investigate the effect of textile fabrics (t-shirt knit and denim cottons) and surface treatments (dry and wet lubricants) on blister formation. 3SP samples consist of bonded elastomeric layers that are surrogates for various dermal layers. These layers display frictional and mechanical properties similar to their anatomical analogues. Blistering was assessed by the measurement of deboned area between layers.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> Denim caused greater blistering than did the t-shirt knit cotton, and both lubricants significantly reduced blister area and surface damage. A triglyceride-based lubricant had a more pronounced effect on blister reduction than corn starch. The triglyceride lubricant used with t-shirt knit cotton resulted in no blisters being formed.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> The performance of the 3SP approach follows previously reported frictional behavior of skin <em>in vivo</em>. The results of textile and surface treatment performance suggest that future 3SP iterations can be focused on specific anatomical sites based on application type.</p></div>]]></content:encoded><description>Background:  Friction blisters occur when shear loading causes the separation of dermal layers. Consequences range from minor pain to life-threatening infection. Past research in blister formation has focused on in vivo experiments, which complicate a mechanics-based study of the phenomenon.Methods:  A Synthetic Skin Simulant Platform (3SP) approach was developed to investigate the effect of textile fabrics (t-shirt knit and denim cottons) and surface treatments (dry and wet lubricants) on blister formation. 3SP samples consist of bonded elastomeric layers that are surrogates for various dermal layers. These layers display frictional and mechanical properties similar to their anatomical analogues. Blistering was assessed by the measurement of deboned area between layers.Results:  Denim caused greater blistering than did the t-shirt knit cotton, and both lubricants significantly reduced blister area and surface damage. A triglyceride-based lubricant had a more pronounced effect on blister reduction than corn starch. The triglyceride lubricant used with t-shirt knit cotton resulted in no blisters being formed.Conclusion:  The performance of the 3SP approach follows previously reported frictional behavior of skin in vivo. The results of textile and surface treatment performance suggest that future 3SP iterations can be focused on specific anatomical sites based on application type.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00539.x" xmlns="http://purl.org/rss/1.0/"><title>Sonophoresis-mediated permeation and retention of peptide dendrimers across human epidermis</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00539.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Sonophoresis-mediated permeation and retention of peptide dendrimers across human epidermis</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Srinivas Mutalik</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Usha Y. Nayak</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rohit Kalra</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Aravind Kumar</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Raghavendra V. Kulkarni</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Harendra S. Parekh</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00539.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00539.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00539.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">101</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">107</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Purpose: </b> The objective of the present study was to assess the effect of sonophoresis on the permeation rate of peptide dendrimers through human skin.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> Peptide dendrimers containing arginine and histidine as terminal amino acids and having varying positive charges (arginine group: R4, R8 and R16 dendrimers, having 4<sup>+</sup>, 8<sup>+</sup> and 16<sup>+</sup> charges, respectively; histidine group: H4, H8 and H16 dendrimers, having 4<sup>+</sup>, 8<sup>+</sup> and 16<sup>+</sup> charges, respectively) were synthesized by Fmoc solid-phase peptide synthesis. The <em>in vitro</em> skin permeation studies were conducted using vertical-type diffusion cells and ultrasound was applied using a probe sonicator to the donor solution. The effects of varying concentrations of dendrimer with differing pH of the donor solution on the permeation rate were studied.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> All the dendrimers exhibited significantly (<em>P</em>&lt;0.05) higher permeation rates with the application of ultrasound in comparison with passive diffusion studies (without ultrasound). High concentrations of H4 and R4 dendrimers were found in the receptor media compared with other dendrimers at all the concentrations tested, indicating appreciable permeation of low-molecular-weight dendrimers across the skin, assisted by sonophoresis. The opposite was true when assessing dendrimer ‘retention’ in skin, where it was shown to improve upon increasing dendrimer generation/molecular weight. Negligible loss of all the dendrimers (&lt;2%) during skin permeation studies indicates that neither skin nor ultrasound adversely affects the stability of dendrimers.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> The present study reveals the successful application of sonophoresis in enhancing the permeation of peptide dendrimers across human skin.</p></div>]]></content:encoded><description>Purpose:  The objective of the present study was to assess the effect of sonophoresis on the permeation rate of peptide dendrimers through human skin.Methods:  Peptide dendrimers containing arginine and histidine as terminal amino acids and having varying positive charges (arginine group: R4, R8 and R16 dendrimers, having 4+, 8+ and 16+ charges, respectively; histidine group: H4, H8 and H16 dendrimers, having 4+, 8+ and 16+ charges, respectively) were synthesized by Fmoc solid-phase peptide synthesis. The in vitro skin permeation studies were conducted using vertical-type diffusion cells and ultrasound was applied using a probe sonicator to the donor solution. The effects of varying concentrations of dendrimer with differing pH of the donor solution on the permeation rate were studied.Results:  All the dendrimers exhibited significantly (P&lt;0.05) higher permeation rates with the application of ultrasound in comparison with passive diffusion studies (without ultrasound). High concentrations of H4 and R4 dendrimers were found in the receptor media compared with other dendrimers at all the concentrations tested, indicating appreciable permeation of low-molecular-weight dendrimers across the skin, assisted by sonophoresis. The opposite was true when assessing dendrimer ‘retention’ in skin, where it was shown to improve upon increasing dendrimer generation/molecular weight. Negligible loss of all the dendrimers (&lt;2%) during skin permeation studies indicates that neither skin nor ultrasound adversely affects the stability of dendrimers.Conclusion:  The present study reveals the successful application of sonophoresis in enhancing the permeation of peptide dendrimers across human skin.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00541.x" xmlns="http://purl.org/rss/1.0/"><title>Ability to estimate relative percutaneous penetration via a surrogate maker – trans epidermal water loss?</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00541.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Ability to estimate relative percutaneous penetration via a surrogate maker – trans epidermal water loss?</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Xiaoying Hui</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Rania Elkeeb</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Heldi Chan</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Howard I. Maibach</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00541.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00541.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00541.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">108</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">113</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Aims: </b> This study measures the dynamic change of the trans-epidermal water loss (TEWL) rate and in vitro skin permeation data of tritiated water and [<sup>14</sup>C]-clonidine HCl in order to refine our knowledge in the relationship between percutaneous penetration and TEWL.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Measures: </b> TEWL values were measured before and during the experimental period. Single application of tritiated water and [<sup>14</sup>C]-clonidine HCl were dosed at the same time on dermatomed human skin samples collected from 12 donors in a flow through diffusion cell system. Radioactivity of absorbed dose: stratum corneum, epidermis, dermis, receptor fluid collected every 4 hours, as well as removable dose residue was counted to determine accountability, percent dose, μg equivalent, and flux rate. These data were further combined with TEWL values to analyze their possible relationship.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> Results showed that baseline TEWL values correlated with the thickness of dermatomed skin (<em>r</em>=−0.44, <em>P</em>=0.007), and with tritiated water fluxes (<em>r</em>=0.34, <em>P</em>=0.04) and [<sup>14</sup>C]-clonidine HCl (<em>r</em>=0.36; <em>P</em>=0.03). The fluxes of tritiated water and [<sup>14</sup>C]-clonidine HCl were correlated (<em>r</em>=0.67, <em>P</em>&lt;0.001). When TEWL and permeation data were compared, the pattern of tritiated water expressed as a percent dose permeated in receptor fluid resembled the TEWL pattern.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> The methodology described provides evidences of the correlation of TEWL and skin integrity and skin permeation and further demonstrates to be a rapid alternative to tritiated water permeation for measuring skin barrier functions <em>in vitro</em>. To develop TEWL measurement as a possible predictive model to assess <em>in vitro</em> percutaneous absorption, however more chemicals with various physical-chemical properties need to be examined, and the relationships to TEWL and tritiated water flux better defined.</p></div>]]></content:encoded><description>Aims:  This study measures the dynamic change of the trans-epidermal water loss (TEWL) rate and in vitro skin permeation data of tritiated water and [14C]-clonidine HCl in order to refine our knowledge in the relationship between percutaneous penetration and TEWL.Measures:  TEWL values were measured before and during the experimental period. Single application of tritiated water and [14C]-clonidine HCl were dosed at the same time on dermatomed human skin samples collected from 12 donors in a flow through diffusion cell system. Radioactivity of absorbed dose: stratum corneum, epidermis, dermis, receptor fluid collected every 4 hours, as well as removable dose residue was counted to determine accountability, percent dose, μg equivalent, and flux rate. These data were further combined with TEWL values to analyze their possible relationship.Results:  Results showed that baseline TEWL values correlated with the thickness of dermatomed skin (r=−0.44, P=0.007), and with tritiated water fluxes (r=0.34, P=0.04) and [14C]-clonidine HCl (r=0.36; P=0.03). The fluxes of tritiated water and [14C]-clonidine HCl were correlated (r=0.67, P&lt;0.001). When TEWL and permeation data were compared, the pattern of tritiated water expressed as a percent dose permeated in receptor fluid resembled the TEWL pattern.Conclusion:  The methodology described provides evidences of the correlation of TEWL and skin integrity and skin permeation and further demonstrates to be a rapid alternative to tritiated water permeation for measuring skin barrier functions in vitro. To develop TEWL measurement as a possible predictive model to assess in vitro percutaneous absorption, however more chemicals with various physical-chemical properties need to be examined, and the relationships to TEWL and tritiated water flux better defined.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00543.x" xmlns="http://purl.org/rss/1.0/"><title>Buffering capacity of human skin layers: in vitro</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00543.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Buffering capacity of human skin layers: in vitro</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Yue Zheng</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Bahman Sotoodian</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Wei Lai</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Howard I. Maibach</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00543.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00543.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00543.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">114</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">119</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background/purpose: </b> The skin possesses buffering capacity to resist acidic/alkaline aggression. Skin components contribute differently to this buffering capacity. This study investigates buffering capacity in three skin layers: intact stratum corneum (SC), epidermis and dermis.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> Sodium hydroxide (NaOH) and hydrochloric acid (HCl) solutions at 0.025, 0.05 and 0.1 N were applied to skin (3.18 μL/cm<sup>2</sup>). After 30 min, the skin was washed with 1 mL de-ionized water. TEWL and pH measurements were conducted at baseline (before contact with acid or base), 0, 10 and 30 min post exposure, and continued at 0, 10 and 30 min post washing.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> Data indicate that immediately following acid or base exposures, the dermis demonstrates the highest buffering capacity, while with time, intact stratum corneum predominates.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> These findings potentiate advanced understanding of skin's buffering capacity as related to dermatopharmacology and dermatotoxicology.</p></div>]]></content:encoded><description>Background/purpose:  The skin possesses buffering capacity to resist acidic/alkaline aggression. Skin components contribute differently to this buffering capacity. This study investigates buffering capacity in three skin layers: intact stratum corneum (SC), epidermis and dermis.Methods:  Sodium hydroxide (NaOH) and hydrochloric acid (HCl) solutions at 0.025, 0.05 and 0.1 N were applied to skin (3.18 μL/cm2). After 30 min, the skin was washed with 1 mL de-ionized water. TEWL and pH measurements were conducted at baseline (before contact with acid or base), 0, 10 and 30 min post exposure, and continued at 0, 10 and 30 min post washing.Results:  Data indicate that immediately following acid or base exposures, the dermis demonstrates the highest buffering capacity, while with time, intact stratum corneum predominates.Conclusion:  These findings potentiate advanced understanding of skin's buffering capacity as related to dermatopharmacology and dermatotoxicology.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00527.x" xmlns="http://purl.org/rss/1.0/"><title>Improvement of a three-dimensional measurement system for the evaluation of foot edema</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00527.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">Improvement of a three-dimensional measurement system for the evaluation of foot edema</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">M. Hirai</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">H. Iwata</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. Niimi</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">K. Miyazaki</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">A. Koyama</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. Komatsubara</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00527.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00527.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00527.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">120</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">124</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background/aims: </b> This study investigated the accuracy and usefulness of a newly improved three-dimensional measurement system for measuring the volume and circumference at the foot as well as at the calf and ankle.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> Regarding the newly improved device, halogen light was projected from four directions instead of the conventional two directions. The circumference and volume were measured in the morning and evening with and without elastic stockings in 23 healthy subjects.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> The average circumference at the foot calculated using the ‘average method’, in which the circumference of the foot was measured in 10 places every 1 mm and the values were averaged, significantly increased in the evening compared with in the morning. When stockings were applied, the significant differences in the circumference or volume between the morning and evening disappeared at all sites of the leg.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> The newly improved three-dimensional measurement system incorporating the halogen light from four directions, in which the foot circumference was calculated using an ‘average method’, was reliable and useful for evaluating edema at the foot as well as at the calf and ankle. The beneficial effect of elastic stockings on edema prevention was observed at all sites of the leg.</p></div>]]></content:encoded><description>Background/aims:  This study investigated the accuracy and usefulness of a newly improved three-dimensional measurement system for measuring the volume and circumference at the foot as well as at the calf and ankle.Methods:  Regarding the newly improved device, halogen light was projected from four directions instead of the conventional two directions. The circumference and volume were measured in the morning and evening with and without elastic stockings in 23 healthy subjects.Results:  The average circumference at the foot calculated using the ‘average method’, in which the circumference of the foot was measured in 10 places every 1 mm and the values were averaged, significantly increased in the evening compared with in the morning. When stockings were applied, the significant differences in the circumference or volume between the morning and evening disappeared at all sites of the leg.Conclusion:  The newly improved three-dimensional measurement system incorporating the halogen light from four directions, in which the foot circumference was calculated using an ‘average method’, was reliable and useful for evaluating edema at the foot as well as at the calf and ankle. The beneficial effect of elastic stockings on edema prevention was observed at all sites of the leg.</description></item><item rdf:about="http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00528.x" xmlns="http://purl.org/rss/1.0/"><title>The linear excisional wound: an improved model for human ex vivo wound epithelialization studies</title><link>http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00528.x</link><dc:title xmlns:dc="http://purl.org/dc/elements/1.1/">The linear excisional wound: an improved model for human ex vivo wound epithelialization studies</dc:title><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Amilcar Ezequiel Rizzo</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Laurel A. Beckett</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">Brian S. Baier</dc:creator><dc:creator xmlns:dc="http://purl.org/dc/elements/1.1/">R. Rivkah Isseroff</dc:creator><dc:date xmlns:dc="http://purl.org/dc/elements/1.1/">2012-02-01T00:00:00-05:00</dc:date><dc:identifier xmlns:dc="http://purl.org/dc/elements/1.1/">doi:10.1111/j.1600-0846.2011.00528.x</dc:identifier><dc:rights xmlns:dc="http://purl.org/dc/elements/1.1/"/><dc:publisher xmlns:dc="http://purl.org/dc/elements/1.1/">John Wiley &amp; Sons, Inc.</dc:publisher><prism:doi xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">10.1111/j.1600-0846.2011.00528.x</prism:doi><prism:url xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">http://dx.doi.org/10.1111%2Fj.1600-0846.2011.00528.x</prism:url><prism:startingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">125</prism:startingPage><prism:endingPage xmlns:prism="http://prismstandard.org/namespaces/1.2/basic/">132</prism:endingPage><content:encoded xmlns:content="http://purl.org/rss/1.0/modules/content/"><![CDATA[<div class="para" xmlns:ol="http://www.wiley.com/namespaces/ol/xsl-lib" xmlns="http://www.w3.org/1999/xhtml"><p><b>Background/purpose: </b> Wound healing is a complex process that involves multiple intercellular and intracellular processes and extracellular interactions. Explanted human skin has been used as a model for the re-epithelialization phase of human wound healing. The currently used standard technique uses a circular punch biopsy tool to make the initial wound. Despite its wide use, the geometry of round wounds makes it difficult to measure them reliably.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Methods: </b> Our group has designed a linear wounding tool, and compared the variability in <em>ex vivo</em> human linear and circular wounds.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Results: </b> An <em>F</em> test for differences in variances demonstrated that the linear wounds provided a population of wound size measurements that was 50% less variable than that obtained from a group of matched circular wounds. This reduction in variability would provide substantial advantages for the linear wound technique over the circular wound punch technique, by reducing the sample sizes required for comparative studies of factors that alter healing.</p></div><div class="para" xmlns="http://www.w3.org/1999/xhtml"><p><b>Conclusion: </b> This linear wounding tool thus provides a method for wounding that is standardized, provides minimal error in wound gap measurements, and is easily reproducible. We demonstrate its utility in an <em>ex vivo</em> model for the controlled investigation of human skin wounds.</p></div>]]></content:encoded><description>Background/purpose:  Wound healing is a complex process that involves multiple intercellular and intracellular processes and extracellular interactions. Explanted human skin has been used as a model for the re-epithelialization phase of human wound healing. The currently used standard technique uses a circular punch biopsy tool to make the initial wound. Despite its wide use, the geometry of round wounds makes it difficult to measure them reliably.Methods:  Our group has designed a linear wounding tool, and compared the variability in ex vivo human linear and circular wounds.Results:  An F test for differences in variances demonstrated that the linear wounds provided a population of wound size measurements that was 50% less variable than that obtained from a group of matched circular wounds. This reduction in variability would provide substantial advantages for the linear wound technique over the circular wound punch technique, by reducing the sample sizes required for comparative studies of factors that alter healing.Conclusion:  This linear wounding tool thus provides a method for wounding that is standardized, provides minimal error in wound gap measurements, and is easily reproducible. We demonstrate its utility in an ex vivo model for the controlled investigation of human skin wounds.</description></item></rdf:RDF>
