Physiologic modeling of cyclosporin kinetics in rat and man
- 1 February 1991
- journal article
- research article
- Published by Springer Science and Business Media LLC in Journal of Pharmacokinetics and Biopharmaceutics
- Vol. 19 (1), 21-50
- https://doi.org/10.1007/bf01062191
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- A Model to Account for the Variation in Cyclosporin Binding to Plasma Lipids in Transplant PatientsTherapeutic Drug Monitoring, 1988
- CyclesporinTherapeutic Drug Monitoring, 1988
- Pharmacokinetics of cyclosporin: influence of rate of constant intravenous infusion in renal transplant patients.British Journal of Clinical Pharmacology, 1987
- Cyclosporin: measurement of fraction unbound in plasmaJournal of Pharmacy and Pharmacology, 1987
- Clinical Pharmacokinetics of CyclosporinClinical Pharmacokinetics, 1986
- CYCLOSPORIN, BLOOD-BRAIN BARRIER, AND MULTIPLE SCLEROSISThe Lancet, 1985
- Prediction of diazepam disposition in the rat and man by a physiologically based pharmacokinetic modelJournal of Pharmacokinetics and Biopharmaceutics, 1983
- Tissue Perfusion and Distribution of Cardiac Output During Ketamine Anesthesia in Normovolemic RatsActa Anaesthesiologica Scandinavica, 1980
- Hepatic clearance of drugs. I. Theoretical considerations of a “well-stirred” model and a “parallel tube” model. Influence of hepatic blood flow, plasma and blood cell binding, and the hepatocellular enzymatic activity on hepatic drug clearanceJournal of Pharmacokinetics and Biopharmaceutics, 1977
- In vitro-in vivo correlation of drug metabolism-deamination of 1-β-d-arabinofuranosylcytosineBiochemical Pharmacology, 1972