BERNASQUÉ, Antoine; CARIO, Muriel; KRISA, Stéphanie; LECOMTE, Sophie; FAURE, Chrystel

doi:10.1016/j.ejpb.2023.09.007

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BERNASQUÉ, Antoine
Chimie et Biologie des Membranes et des Nanoobjets [CBMN]

CARIO, Muriel
BoRdeaux Institute in onCology [Inserm U1312 - BRIC]

KRISA, Stéphanie
Unité de Recherche Œnologie [Villenave d'Ornon] [OENO]

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European Journal of Pharmaceutics and Biopharmaceutics. 2023-10, vol. 191, p. 303-314

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Our previous work showed that the size, elasticity and charge of multi-lamellar liposomes (MLLs) could not be considered separately to predict the fate of MLLs in the skin [1]. Based on this study, we developed several MLLs formulations containing a corticosteroid, betamethasone 17-valerate (B17) to transport the drug into the stratum corneum, living epidermis, dermis or through the skin. MLLs encapsulation efficiency was found to exceed 74 +/- 3 % in all cases. In addition, we showed that MLLs protected the corticosteroid from thermal degradation. Comparing the penetration depth of all MLLs within artificial skin measured by Raman imaging, we established an equation for its determination, given the MLLs elasticity and size. This equation was verified experimentally on human explants: quantification of B17 in each skin layer, as well as its transdermal passage by ultra-high performance liquid chromatography, confirmed that B17 was predominantly and significantly transported in the desired layer. Eventually, we showed the benefits in using B17-loaded MLLs instead of a B17-containing pharmaceutical cream in terms of B17 penetration and thermal degradation.< Réduire

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Thermal protection

Skin penetration prediction

Raman imaging

Betamethasone-17-valerate skin distribution

Multi -lamellar liposomes

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Prediction of the penetration depth of multi-lamellar liposomes in artificial skin. Application to the vectorization of corticosteroid in human skin

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