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In vivo measurements of diffuse reflectance and time-resolved autofluorescence emission spectra of basal cell carcinomas
Article first published online: 6 FEB 2012
DOI: 10.1002/jbio.201100126
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
Thompson, A. J., Coda, S., Sørensen, M. B., Kennedy, G., Patalay, R., Waitong-Brämming, U., De Beule, P. A. A., Neil, M. A. A., Andersson-Engels, S., Bendsøe, N., French, P. M. W., Svanberg, K. and Dunsby, C. (2012), In vivo measurements of diffuse reflectance and time-resolved autofluorescence emission spectra of basal cell carcinomas. J. Biophoton., 5: 240–254. doi: 10.1002/jbio.201100126
Publication History
- Issue published online: 5 MAR 2012
- Article first published online: 6 FEB 2012
- Manuscript Accepted: 12 JAN 2012
- Manuscript Revised: 23 DEC 2011
- Manuscript Received: 18 NOV 2011
Funded by
- Engineering and Physical Sciences Research Council (EPSRC EP/F040202/1)
- Photonics-4-Life European Network (FP7-ICT-2007-2, 224014)
- SKINSPECTION project (FP7-HEALTH-2007-A, 201577)
- EPSRC funded Ph.D. studentship
- PIEp
- Swedish innovation initiative
- Royal Society Wolfson Research Merit Award
- Abstract
- References
- Cited By
Keywords:
- fluorescence;
- fluorescence lifetime;
- diffuse reflectance;
- skin cancer;
- spectrometer;
- fibre probe
Abstract
We present a clinical investigation of diffuse reflectance and time-resolved autofluorescence spectra of skin cancer with an emphasis on basal cell carcinoma. A total of 25 patients were measured using a compact steady-state diffuse reflectance/fluorescence spectrometer and a fibre-optic-coupled multispectral time-resolved spectrofluorometer. Measurements were performed in vivo prior to surgical excision of the investigated region. Singular value decomposition was used to reduce the dimensionality of steady state diffuse reflectance and fluorescence spectra. Linear discriminant analysis was then applied to the measurements of basal cell carcinomas (BCCs) and used to predict the tissue disease state with a leave-one-out methodology. This approach was able to correctly diagnose 87% of the BCCs. With 445 nm excitation a decrease in the spectrally averaged fluorescence lifetime was observed between normal tissue and BCC lesions with a mean value of 886 ps. Furthermore, the fluorescence lifetime for BCCs was lower than that of the surrounding healthy tissue in all cases and statistical analysis of the data revealed that this decrease was significant (p = 0.002). (© 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim)

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