Bioinversion of R-flurbiprofen to S-flurbiprofen at various dose levels in rat, mouse, and monkey

被引:23
作者
Leipold, DD [1 ]
Kantoci, D [1 ]
Murray, D [1 ]
Quiggle, DD [1 ]
Wechter, WJ [1 ]
机构
[1] Encore Pharmaceut Inc, Riverside, CA 92507 USA
关键词
pharmacokinetics; preclinical model; aryl propionic acids; chiral bioinversion; metabolism;
D O I
10.1002/chir.20053
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Information about the potential and extent of bioinversion of chiral drugs in laboratory animal species and humans is critical to the interpretation of preclinical pharm-tox studies with these drugs. Unlike in the dog, guinea pig, and rabbit, in humans the 2-arylpropionic acid (APA) R-flurbiprofen (R-FB) undergoes very little bioinversion to S-flurbiprofen. The primary objective of this research was to identify laboratory animal species with an R- to S-bioinversion profile similar to humans. Detailed evaluations of the pharmacokinetics parameters of R-flurbiprofen in male and female rats and mice, and male nude rats and monkeys demonstrated R- to S-bioinversion of 30% (average) in monkeys, 15-24% in mice, and -4% in rats. To date, no laboratory animal species has been identified with an R-flurbiprofen bioinversion profile identical to humans. However, the rat has a bioinversion profile sufficiently similar to humans to be useful for preclinical pharm-tox studies employing relatively short-term dosing regimens. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:379 / 387
页数:9
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