Abstract

PurposeTo image SDS distribution across different skin regions, to compare the permeability difference between porcine and human skin, and to evaluate the interaction between SDS and skin.MethodsFull thickness porcine and human skin was treated with acyl chain perdeuterated SDS (SDS-d25) at room temperature and at 34 °C for 3, 24 and 40 h. SDS distribution in skin was monitored by confocal Raman and IR microspectroscopic imaging. Permeation profiles of SDS-d25 in skin were derived from the band intensities of the CD2 stretching vibrations. The interaction between SDS and skin was monitored through the CH2 and CD2 stretching frequencies and the Amide I and II spectral region.ResultsSDS-d25 penetrates both porcine and human skin in a time and temperature-dependent manner, with slightly higher permeability through the stratum corneum (SC) in porcine skin. When SDS permeates into the SC, its chains are more ordered compared to SDS micelles. The secondary structure of keratin in the SC is not affected by SDS-d25.ConclusionThe spatial distribution of SDS-d25 in skin was obtained for the first time. Infrared microscopic imaging provides unique opportunities to measure concentration profiles of exogenous materials in skin and offers insights to interaction between permeants and skin.Electronic supplementary materialThe online version of this article (doi:10.1007/s11095-012-0748-y) contains supplementary material, which is available to authorized users.

Highlights

  • Stratum corneum (SC), the topmost layer of the epidermis, provides a vital barrier function in intact skin

  • Confocal Raman microscopy provides a convenient approach to track the permeation of exogenous agents in skin without complicated sample preparation

  • Our results indicate that we have detected 5–16 % of the applied dosage in porcine skin and 1–17 % in human skin, excluding the 34 °C 40 h treatment

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Summary

Introduction

Stratum corneum (SC), the topmost layer of the epidermis, provides a vital barrier function in intact skin. The lateral packing and lamellar phases of the highly ordered SC lipid matrix have been well studied by various biophysical techniques. In both human and porcine SC, two lamellar phases have been identified by X-ray diffraction [2,3] whereas the nature of the lateral lipid packing, as studied by X-ray and FTIR [4,5,6,7] is shown to vary between species. SC lipids are predominantly packed in ordered orthorhombic and hexagonal phases with some (small amounts) disordered lipid likely present. Overall at skin surface temperature (~34 °C), a fair amount of orthorhombic phase remains in human with lesser amounts in pig SC

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