Physiologic modeling of cyclosporin kinetics in rat and man

Abstract

A physiologic pharmacokinetic model of cyclosporin has been developed in the rat aimed at predicting the time course of drug concentrations in blood, organs, and tissues. The model assumes that tissue distribution is perfusion-rate limited and that each tissue acts as a well-stirred compartment. The unbound equilibrium distribution ratios as well as the… (More)
DOI: 10.1007/BF01062191

17 Figures and Tables

Topics

  • Presentations referencing similar topics