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International audience; In the context of cutaneous carcinoma diagnosis based on in vivo optical biopsy, Diffuse Reflectance (DR) spectra, acquired using a Spatially Resolved (SR) sensor configuration, can be analyzed to distinguish healthy from pathological tissues. The present contribution aims at studying the depth distribution of SR-DR-detected photons in skin from the perspective of analyzing how these photons contribute to acquired spectra carrying local physiological and morphological information. Simulations based on modified Cuda Monte Carlo Modeling of Light transport were performed on a five-layer human skin optical model with epidermal thickness, phototype and dermal blood content as variable parameters using (i) wavelength-resolved scattering and absorption properties and (ii) the geometrical configuration of a multi-optical fiber probe implemented on an SR-DR spectroscopic device currently used in clinics. Through histograms of the maximum probed depth and their exploitation, we provide numerical evidence linking the characteristic penetration depth of the detected photons to their wavelengths and four source–sensor distances, which made it possible to propose a decomposition of the DR signals related to skin layer contributions.

Published in SPIE Proceedings Volume 11640, Optical Interactions with Tissue and Cells XXXII, 116400H (2021); International audience; In the context of cutaneous carcinoma in vivo diagnosis, Diffuse Relectance (DR) acquired using Spatially Resolved (SR) optical biopsy, can be analysed to discard healthy from pathological areas. Indeed, carcinogenesis induces local morphological and metabolic changes affecting the skin optical answer to white light excitation. The present contribution aims at studying the epidermis thickness impact on the path and propagation depth distribution of DR photons in skin in the perspective of analyzing how these photons contribute to the corresponding acquired spectra carrying local physiological information from the visited layers. Modified CudaMCML-based simulations were performed on a five-layer human skin optical model using (i) wavelength-resolved scattering and absorption properties and (ii) the geometrical configuration of a multi-optical fiber probe implemented on a SR-DR spectroscopic device currently used in clinics. Through maps of scattering events and histograms of maximum probed depth, we provide numerical evidences linking the characteristic penetration depth of the detected photons to their wavelengths and four source-sensor distances for thin, intermediate and wide skin thicknesses model. The study provides qualitative and quantitative tools that can be useful during the design of an optical SR-DR spectroscopy biopsy device.

International audience; In this study, the changes in Spatially Resolved Diffuse Reflectance and AutoFluorescence spectra acquired on ex vivo human skin during optical clearing process (topical application) are investigated and their impact on skin optical properties (absorption, scattering and fluorescence) analyzed using inverse problem solving and multidimensional data processing approaches.

In the context of cutaneous carcinoma in vivo diagnosis, Diffuse Relectance (DR) and skin endogenous fluores- cence (AF) spectra, acquired using Spatially Resolved (SR) multimodal optical biopsy, can be analysed to discard healthy from pathological areas. Indeed, carcinogenesis induces morphological and metabolic changes affecting endogenous fluorophores such as for instance elastosis and enzymatic degradation of collagen fluorescence in the dermis or decreased NADH fluorescence in the epidermis. The present contribution aims at studying the path and propagation depth distribution of DR and AF photons in skin in the perspective of analyzing how these photons contribute to the corresponding acquired spectra carrying local physiological information. Modified CudaMCML-based simulations were performed on a five-layer human skin optical model with (i) wavelength resolved scattering, absorption and endogenous fluorescence properties and (ii) multiple fiber optic probe ge- ometrical configuration of a SR-DR and -AF spectroscopic device. The simulation results provided numerical evidences of the behaviour of detected photons in the tissue. In particular, we succeeded in linking the character- istic penetration depth of the detected photons to their wavelengths and the source-sensor distance. In addition, we managed to identify the region where the fluorescence events associated with the AF spectrum photon take place. The study provides qualitative and quantitative tools that can be useful during the design of an optical multimodal biopsy device.