Noninvasive evaluation of the skin barrier in reconstructed human epidermis using speckle analysis: Correlation with Raman microspectroscopy

Author:

Habib Léa12,Nassif Léa Abi3,Abboud Marie3,Michael‐Jubeli Rime2,Tfayli Ali2,Lteif Roger1ORCID

Affiliation:

1. Laboratoire d’étude cinétique en milieu hétérogène (LECH) Faculté des Sciences Université Saint Joseph Beirut Lebanon

2. Unité Universitaire Interdisciplinaire Lip(Sys)2: Lipides, Systèmes analytiques et biologiques, Faculté de pharmacie Université Paris‐Saclay Orsay France

3. Physics Department, UR TVA, Faculté des sciences Université Saint Joseph Beirut Lebanon

Abstract

AbstractBackgroundReconstructed epidermis models, obtained from 3D keratinocytes culture, have gained significant prominence as prototypes for safety and efficacy testing in skin research. To effectively evaluate these models, it is essential to perform molecular and functional characterization. The skin's barrier function is one of the essential aspects of the epidermis that needs to be assessed. A noninvasive method is thus required for the evaluation of the skin barrier in these models. With this perspective, the aim of this feasibility study is to apply the speckle technique for the assessment of the skin barrier in the Reconstructed Human Epidermis (RHE).Materials and methodsSpeckle analysis as well as Raman microspectroscopy were performed on RHE samples at two maturation days, D17 and D20.ResultsBetween D17 and D20, our study showed an increase in various Raman parameters, including stratum corneum percentage, lateral lipid packing, lipid‐to‐protein ratio, and protein secondary structure. Furthermore, the degree of light polarization and the speckle grain size also increased over this period.ConclusionThe speckle technique proved to be effective for evaluating the skin barrier in Reconstructed Human Epidermis (RHE) models. Comparison with Raman validates this approach and provides comprehensive molecular and functional characterization of reconstructive skin models.

Publisher

Wiley

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