The Effects of UV Emission from Compact Fluorescent Light Exposure on Human Dermal Fibroblasts and Keratinocytes In Vitro
Version of Record online: 20 JUL 2012
© 2012 Wiley Periodicals, Inc. Photochemistry and Photobiology © 2012 The American Society of Photobiology
Photochemistry and Photobiology
Volume 88, Issue 6, pages 1497–1506, November/December 2012
How to Cite
Mironava, T., Hadjiargyrou, M., Simon, M. and Rafailovich, M. H. (2012), The Effects of UV Emission from Compact Fluorescent Light Exposure on Human Dermal Fibroblasts and Keratinocytes In Vitro. Photochemistry and Photobiology, 88: 1497–1506. doi: 10.1111/j.1751-1097.2012.01192.x
- Issue online: 29 OCT 2012
- Version of Record online: 20 JUL 2012
- Accepted manuscript online: 23 JUN 2012 09:21AM EST
- Received 25 April 2012, accepted 13 June 2012
Figure S1. TiO2 imaged by TEM and Gaussian particles size distribution histograms. (a) and (c) rutile 16 ± 3 nm particles, (b) and (d) anatase 134 ± 73 nm particles.
Figure S2. X-ray diffraction spectra of TiO2. (a) rutile, (b) anataise.
Figure S3. Cell aspect ratio for the CF-29 dermal fibroblasts. Samples with rutile unexposed and double exposed to CFL respectively and control; cell area (b) of dermal fibroblasts CF-29 samples with rutile unexposed and double exposed to CFL respectively and control.
Figure S4. (a) MTS results for the CF-29 cells 2 and 4 days after first exposure to CFL bulb, incandescent light bulb and control. After first exposure (2 days) incandescent bulb and CFL bulb; 4 days after first exposure incandescent bulb, CFL bulb; double exposed samples: incandescent and CFL bulb. (b–d) Confocal images of the cells exposed to different lighting. (b) Unexposed control, (c) double exposure to incandescent light bulb, (d) double exposure to CFL.
Table S1. Zeta-potential of TiO2 nanoparticles.
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