Evaluation of Human Interindividual Variation in Bioactivation of Estragole Using Physiologically Based Biokinetic Modeling-Reference-Cited by-同舟云学术

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Evaluation of Human Interindividual Variation in Bioactivation of Estragole Using Physiologically Based Biokinetic Modeling

Published:2009-11-17 Issue:2 Volume:113 Page:337-348
ISSN:1096-6080
Container-title:Toxicological Sciences
language:en
Short-container-title:

Author:

Punt Ans,Jeurissen Suzanne M.,Boersma Marelle G.,Delatour Thierry,Scholz Gabriele,Schilter Benoît,van Bladeren Peter J.,Rietjens Ivonne M. C. M.

Publisher

Oxford University Press (OUP)

Subject

Toxicology

Link

http://academic.oup.com/toxsci/article-pdf/113/2/337/10940422/kfp272.pdf

Reference42 articles.

1. Metabolism of estragole in rat and mouse and influence of dose size on excretion of the proximate carcinogen 1′-hydroxyestragole;Food Chem. Toxicol.,1987

2. Scaling factors for the extrapolation of in vivo metabolic drug clearance from in vitro data: Reaching a consensus on values of human microsomal protein and hepatocellularity per gram of liver;Curr. Drug Metab.,2007

3. Prediction of interindividual variation in drug plasma levels in vivo from individual enzyme kinetic data and physiologically based pharmacokinetic modeling;Eur. J. Pharm. Sci.,2000

4. Hepatocarcinogenicity of estragole (1-allyl-4-methoxybenzene) and 1′-hydroxyestragole in the mouse and mutagenicity of 1′-acetoxyestragole in bacteria;J. Natl. Cancer Inst.,1976

5. Sensitivity analysis of a physiological model for 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD): Assessing the impact of specific model parameters on sequestration in liver and fat in the rat;Toxicol. Sci.,2000

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