Author:
Yan Li,Ropella Glen E. P.,Park Sunwoo,Roberts Michael S.,Hunt C. Anthony
Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Organic Chemistry,Pharmaceutical Science,Pharmacology,Molecular Medicine,Biotechnology
Reference20 articles.
1. M. Rowland, L. Balant, and C. Peck. Physiologically based pharmacokinetics in drug development and regulatory science: a workshop report (Georgetown University, Washington, DC, May 29–30, 2002). AAPS PharmSci 6:E6(2004).
2. C. A. Hunt, G. E. Ropella, L. Yan, D. Y. Hung, and M. S. Roberts. Physiologically based synthetic models of hepatic disposition. J. Pharmacokinet. Pharmacodyn 33:737–772 (2006).
3. Y. G. Anissimov, and M. S. Roberts. A compartmental model of hepatic disposition kinetics: 1. Model development and application to linear kinetics. J. Pharmacokinet. Pharmacodyn. 29:131–156 (2002).
4. D. Y. Hung, P. Chang, K. Cheung, B. McWhinney, P. P. Masci, M. Weiss, and M. S. Roberts. Cationic drug pharmacokinetics in diseased livers determined by fibrosis index, hepatic protein content, microsomal activity, and nature of drug. J. Pharmacol. Exp. Ther 301:1079–1087 (2002).
5. D. Y. Hung, P. Chang, M. Weiss, and M. S. Roberts. Structure-hepatic disposition relationships for cationic drugs in isolated perfused rat livers: transmembrane exchange and cytoplasmic binding process. J. Pharmacol. Exp. Ther 297:780–789 (2001).