A physiologically based pharmacokinetic model to predict the pharmacokinetics of highly protein-bound drugs and the impact of errors in plasma protein binding

Author:

Ye Min1,Nagar Swati1,Korzekwa Ken1

Affiliation:

1. Department of Pharmaceutical Science; Temple University School of Pharmacy; Philadelphia PA 19140 USA

Funder

National Institutes of Health

Publisher

Wiley

Subject

Pharmacology (medical),Pharmaceutical Science,Pharmacology,General Medicine

Reference49 articles.

1. Commentary: a physiological approach to hepatic drug clearance;Wilkinson;Clin Pharmacol Ther,1975

2. Prediction of human clearance of twenty-nine drugs from hepatic microsomal intrinsic clearance data: an examination of in vitro half-life approach and nonspecific binding to microsomes;Obach;Drug Metab Dispos,1999

3. Kinetic determinants of hepatic clearance: plasma protein binding and hepatic uptake;Baker;Xenobiotica,2007

4. Impact of pH on plasma protein binding in equilibrium dialysis;Kochansky;Mol Pharm,2008

5. A priori prediction of tissue:plasma partition coefficients of drugs to facilitate the use of physiologically-based pharmacokinetic models in drug discovery;Poulin;J Pharm Sci,2000

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