Reconstruction of Drug Dispositions in Vivo from in Vitro Studies Based on Physiological Pharmacokinetic Modeling : From Low-molecular Weight Drugs to Polypeptide Compounds-Reference-Cited by-同舟云学术

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Reconstruction of Drug Dispositions in Vivo from in Vitro Studies Based on Physiological Pharmacokinetic Modeling : From Low-molecular Weight Drugs to Polypeptide Compounds

Published:1989 Issue:4 Volume:109 Page:199-231
ISSN:0031-6903
Container-title:YAKUGAKU ZASSHI
language:en
Short-container-title:YAKUGAKU ZASSHI

Author:

SUGIYAMA Yuichi

Publisher

Pharmaceutical Society of Japan

Subject

Pharmaceutical Science,Pharmacology

Link

https://www.jstage.jst.go.jp/article/yakushi1947/109/4/109_4_199/_pdf

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3. Physiologically based pharmacokinetics of KNI-272, a tripeptide HIV-1 protease inhibitor;Biopharmaceutics & Drug Disposition;1999-05

4. Prediction of the maximal tolerated dose (MTD) and therapeutic effect of anticancer drugs in humans: integration of pharmacokinetics with pharmacodynamics and toxicodynamics;Cancer Treatment Reviews;1995-03

5. RATES OF SYSTEMIC DEGRADATION AND RETICULOENDOTHELIAL SYSTEM UPTAKE OF CALCEIN IN THE DIPALMITOYLPHOSPHATIDYLCHOLINE LIPOSOMES WITH SOYBEAN-DERIVED STEROLS IN MICE;Pharmaceutical Research;1995

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