Abstract

A pharmacokinetic model for percutaneous absorption has been formulated which allows calculation of the drug disposition in the skin, plasma and urine. Allowance is also made for metabolic processes within the skin. The influence of metabolism on the concentrations of the parent molecule and the metabolite in the plasma is discussed.

Original languageEnglish
Pages (from-to)43-51
Number of pages9
JournalInternational Journal of Pharmaceutics
Volume20
Issue number1-2
DOIs
Publication statusPublished - 1984

ASJC Scopus subject areas

  • Pharmaceutical Science

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