Physiological pharmacokinetic model for the distribution and elimination of tenoxicam
- 1 July 1987
- journal article
- research article
- Published by Elsevier in International Journal of Pharmaceutics
- Vol. 37 (3) , 219-226
- https://doi.org/10.1016/0378-5173(87)90032-9
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- MULTI-FORTE, a microcomputer program for modelling and simulation of pharmacokinetic dataComputer Methods and Programs in Biomedicine, 1986
- Physiological model for the pharmacokinetics ofcis-dichlorodiammineplatinum(II) (DDP) in the tumored ratJournal of Pharmacokinetics and Biopharmaceutics, 1985
- Rapid method for the determination of either piroxicam or tenoxicam in plasma using high-performance liquid chromatographyJournal of Chromatography B: Biomedical Sciences and Applications, 1984
- Physiological pharmacokinetic model for distribution and elimination of pentazocine. II. Study in rabbits and scale-up to manInternational Journal of Pharmaceutics, 1984
- Metabolism of tenoxicam in ratsXenobiotica, 1984
- Physiologically Based Pharmacokinetic Modeling: Principles and ApplicationsJournal of Pharmaceutical Sciences, 1983
- Physiological pharmacokinetic model for pentazocine. I. Tissue distribution and elimination in the ratInternational Journal of Pharmaceutics, 1983
- Gastro-intestinal blood loss with high dose tilcotil (Ro 12-0068) and aspirin: an open crossover clinical trial and pharmacokinetic assessment in normal volunteersCurrent Medical Research and Opinion, 1983
- Disposition of sulfadimethoxine in swine: Inclusion of protein binding factors in a pharmacokinetic modelJournal of Pharmacokinetics and Biopharmaceutics, 1982
- Kinetics of uptake, distribution, and excretion of zinc in ratsAnnals of Biomedical Engineering, 1981