Influence of solubility and permeant size on absorption and metabolism of xenobiotics in rabbit skin

Author:

Bast Gabriele E1

Affiliation:

1. Walther-Straub-Institut für Pharmakologie und Toxikologie, Medizinische Fakultät der Ludwig-Maximilians-Universität, Nussbaumstr. 26, 80336 München, Germany

Abstract

1 In order to obtain an understanding of the risks associated with dermal uptake of xenobiotics it is necessary to investigate the principles governing percutaneous absorption and metabolism. The sin gle-pass perfused rabbit ear served as a convenient model for the simultaneous study of absorption and metabolism of a variety of substances. We found: 2 When substances are applied in a lipophilic vehicle the permeation coefficient K P is notably decreased when the distribution coefficient (n-octanol/perfusion buffer (pH 7.4)) Poct. exceeds 2000. KP also decreases with increasing molecular weight. 3 Substances which are in the ionized state at pH 7.4 may have a higher permeation coefficient than would be expected from Poct. or by molecular weight. 4 The partition of a drug from the stratum corneum to the epidermal enzymes controls the extent of its metabo lism. However, substances with increased solubility at physiological pH are metabolized to a lesser extent than expected from their absorption rate.

Publisher

SAGE Publications

Subject

Health, Toxicology and Mutagenesis,Toxicology,General Medicine

Reference20 articles.

1. Scheuplein RJ, Bronaugh RL Percutaneous absorption. In: Biochemistry and physiology of the skin. Goldsmith LA (ed.) Oxford University Press , Oxford, 1983; pp 1255-1295.

2. Identification of Intratissue Sites for Xenobiotic Activation and Detoxication

3. Distribution of xenobiotic metabolizing enzymes in skin

4. Drug Metabolism in the Skin

5. Cutaneous Metabolism of Xenobiotics

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