Date of download: 6/25/2016 Copyright © 2016 SPIE. All rights reserved. Overview (a), images of the λ-stack (b) and spectra of ROI 1 and 2 (c) of a 24.

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Date of download: 6/25/2016 Copyright © 2016 SPIE. All rights reserved. Overview (a), images of the λ-stack (b) and spectra of ROI 1 and 2 (c) of a 24 h penetration skin sample. The given wavelengths of the λ-stack describe the center of the 20 nm wide wavebands. Figure Legend: From: Evaluation and quantification of spectral information in tissue by confocal microscopy J. Biomed. Opt. 2012;17(10): doi: /1.JBO

Date of download: 6/25/2016 Copyright © 2016 SPIE. All rights reserved. Overview (a), images of the λ-Stack, (b) spectra of ROI 1 and 2, (c) of an untreated skin sample. The given wavelengths of the λ- stack describe the center of the 20 nm wide wavebands. Figure Legend: From: Evaluation and quantification of spectral information in tissue by confocal microscopy J. Biomed. Opt. 2012;17(10): doi: /1.JBO

Date of download: 6/25/2016 Copyright © 2016 SPIE. All rights reserved. The graphs show the results of the varying PMT (a) and focus (b) settings. The image sequences illustrate the changes in the data when varying the PMT voltage and the focus depth, respectively. Figure Legend: From: Evaluation and quantification of spectral information in tissue by confocal microscopy J. Biomed. Opt. 2012;17(10): doi: /1.JBO

Date of download: 6/25/2016 Copyright © 2016 SPIE. All rights reserved. Emission spectra of untreated porcine skin and the fluorescent dye Nile Red (Excitation: 476 nm). The spectral data was measured using the confocal microscope. The normalized presentation of the data shows the distinguishable emission peaks and the spectral overlap. Figure Legend: From: Evaluation and quantification of spectral information in tissue by confocal microscopy J. Biomed. Opt. 2012;17(10): doi: /1.JBO

Date of download: 6/25/2016 Copyright © 2016 SPIE. All rights reserved. Determination of the appropriate value for UIx. The graph shows the UI0.7, UI0.8 and UI0.9 values for 0.2 μg/mL, 1 μg/mL and 2 μg/mL Nile Red reference skin samples. It is not possible to discriminate the 0.2 μg/mL and 1 μg/mL sample when using UI0.9. Figure Legend: From: Evaluation and quantification of spectral information in tissue by confocal microscopy J. Biomed. Opt. 2012;17(10): doi: /1.JBO

Date of download: 6/25/2016 Copyright © 2016 SPIE. All rights reserved. Skin penetration study results (n=20 per penetration period). Data are presented in mean ±SD. *P<0.05 and ***P<0.001 evaluated by paired Student’s t-test. The 24 h samples show a significantly higher uptake of Nile Red. Figure Legend: From: Evaluation and quantification of spectral information in tissue by confocal microscopy J. Biomed. Opt. 2012;17(10): doi: /1.JBO

Date of download: 6/25/2016 Copyright © 2016 SPIE. All rights reserved. Overlay of the intensity based confocal images of the skin and the spectrally resolved dye distribution (shown in red, please refer to the online version of this manuscript) for the four time periods. Figure Legend: From: Evaluation and quantification of spectral information in tissue by confocal microscopy J. Biomed. Opt. 2012;17(10): doi: /1.JBO