1AARONS L.Physiologically based pharmacokinetic modelling:a sound mechanistic basis is needed[J].Br J clin Pharmacol,2005,60(6):581-583.
2WU G.Fit fluctuation blood drug concentration:a beginner's first note[J].Pharmacol Res,1996,33(6):379-383.
3WU G.Sensitivity analysis of PK parameters in one-compartment models[J].Pharmacol Res,2000,41(4):445-453.
4SCHAIQuEVICH P,NISELMAN A,RUBIO M.Comparison of two compartmental models for describing ranitidine's plasmatic profiles[J].Pharmacoll Res,2002,45(5):399-405.
5UPTON R N.The two-compartment recirculatory pharmacokinetic model--an introduction to recirculatory pharmacokinetic concepts[J].Br J Anaesth,2004,92(4):475-484.
6KUIPERS J A,BOER F,OLIEMAN W,et al.First-pass Lung uptake and pulmonary clearance of propofol[J].Anesthesiology,1999,91(6):1780-1787.
8NESTOROV I.whole body pharmacokinetic models[J].Clin Pharmacokinet,2003,42(10):883-906.
9POULIN P,THEIL F P.Prediction of pharmacokinetics prior to in vivo studies.Ⅱ.Generic physiologically based pharmacokinetic models of drug disposition[J].J Pharm Sci,2002,91(5):1358-1370.
8A. Riitschel and P S Banaerjee. Physiologically Based Pharmarcokinetic Aodels: Priciples, Applications, Limitations, and Outlook. Meth. Fred. Exp. Clin. Pharmarcol. 1986,8:603-614.
9R H Smith, D H Hunt, A B Seifen, A. Ferrari and D S Thompson, Physiological Model for Procain in Humans during and Following Intravenous Infusion J[J]. Pharm. Sci. 1979,68:1016-1019.
10J H Lin, S. Awazu and M Harno, In Vitro and In Evaluation of the Tissue-to-Blood Partition Conefficient for Physiologically Based Pharmacokinetic Models J [J]. Pharmocokinet.Biopharm.1982, 10: 637-642.