Modeling Drug Disposition and Drug–Drug Interactions Through Hypothesis-Driven Physiologically Based Pharmacokinetics: a Reversal Translation Perspective-Reference-Cited by-同舟云学术

Modeling Drug Disposition and Drug–Drug Interactions Through Hypothesis-Driven Physiologically Based Pharmacokinetics: a Reversal Translation Perspective

Published:2017-12-05 Issue:3 Volume:43 Page:369-371
ISSN:0378-7966
Container-title:European Journal of Drug Metabolism and Pharmacokinetics
language:en
Short-container-title:Eur J Drug Metab Pharmacokinet

Author:

Li Guo-Fu,Zheng Qing-Shan

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pharmacology

Link

http://link.springer.com/article/10.1007/s13318-017-0452-8/fulltext.html

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4. Huang W, Nakano M, Sager J, Ragueneau-Majlessi I, Isoherranen N. Physiologically based pharmacokinetic model of the CYP2D6 probe atomoxetine: extrapolation to special populations and drug–drug interactions. Drug Metab Dispos. 2017;45(11):1156–65.

5. Yoshida K, Sun B, Zhang L, Zhao P, Abernethy DR, Nolin TD, et al. Systematic and quantitative assessment of the effect of chronic kidney disease on CYP2D6 and CYP3A4/5. Clin Pharmacol Ther. 2016;100(1):75–87.

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