| Literature DB >> 18228598 |
Koji Yamaguchi1, Tetsuya Mitsui, Yoshinori Aso, Kenji Sugibayashi.
Abstract
The purpose of this study was to evaluate structure-permeability relationships for chemicals through stratum corneum (SC) and viable epidermis/dermis (VED). In vitro skin permeation of ten compounds through excised rat skin was analyzed based on a two-layer diffusion model and the diffusion coefficients in SC (D(SC)) and VED (D(VED)) were determined. The relationships between the permeation parameters and the physicochemical parameters (octanol-water partition coefficient (log K(o/w)), and hydrogen bond donor number (HBD)) of the compounds were analyzed. D(SC) increased as lipophilicity increased, whereas D(VED) decreased for log K(o/w) > 2. Increases in log K(o/w) caused a decrease in the permeability coefficient from SC through VED (P(VED/SC)) for log K(o/w) > 1. The simulation study suggests that the in vitro skin permeation of a highly lipophilic compound is strongly controlled by skin thickness due to low diffusivity in VED. The present study suggests that VED act as a considerable permeation barrier for highly lipophilic compounds due to low diffusivity. (c) 2008 Wiley-Liss, Inc. and the American Pharmacists AssociationEntities:
Mesh:
Year: 2008 PMID: 18228598 DOI: 10.1002/jps.21330
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534