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氟比洛芬在人和大鼠体内的立体选择性药代动力学

Stereoselective pharmacokinetics of flurbiprofen in humans and rats.

作者信息

Jamali F, Berry B W, Tehrani M R, Russell A S

机构信息

Faculty of Pharmacy and Pharmaceutical Sciences, University of Alberta, Edmonton, Canada.

出版信息

J Pharm Sci. 1988 Aug;77(8):666-9. doi: 10.1002/jps.2600770805.

Abstract

Flurbiprofen, a 2-arylpropionic acid (2-APA) nonsteroidal anti-inflammatory drug (NSAID), exists as racemate and is used as such. Although the activity of 2-APAs is due mainly to their S-enantiomers, information on the pharmacokinetics of flurbiprofen is usually based on the measurement of total concentrations of S- and R-flurbiprofen. In this work, the pharmacokinetics of flurbiprofen enantiomers following single doses were studied in humans and rats. Upon iv administration of 10 mg/kg of racemic flurbiprofen to male Sprague-Dawley rats, the plasma concentrations were consistently higher for S-flurbiprofen than for R-flurbiprofen (AUC = 134 +/- 39 versus 41 +/- 9 mg.L-1 h). In bile duct-cannulated rats, the biliary excretion contained only 3.6-5.2% of the dose as conjugated flurbiprofen (S:R = 1.2-2.1). After administration of R-flurbiprofen to the rat, both enantiomers were found in plasma [AUC(R):AUC(S) = 0.10-0.16], indicating a limited extent of enantiomeric bioinversion. This is consistent with the previously reported limited extent of flurbiprofen uptake into fat. In healthy volunteers also, significant stereoselectivity was observed in the plasma concentration of the drug after 100-mg oral racemic doses [AUC-(S):AUC(R) = 45.4 +/- 12.7:40.1 +/- 14.3 mg.L-1.h]. As compared with the R-enantiomer, S-flurbiprofen has a smaller volume of distribution (7.23 +/- 1.9 versus 8.41 +/- 3.0 L) and total clearance (1.23 +/- 0.34 versus 1.47 +/- 0.50 L/h), but an equal half-life (4.21 +/- 1.2 versus 4.18 +/- 1.3 h). In urine, on the other hand, the R-configuration was predominant, as greater amounts of the R-enantiomer were found both as conjugated flurbiprofen and as an unidentified metabolite. Negligible amounts of intact flurbiprofen enantiomers were detected in urine. The observed stereoselectivity in humans cannot be attributed to enantiomeric bioinversion, as S-flurbiprofen was not detected in plasma and urine after oral administration of R-flurbiprofen.

摘要

氟比洛芬是一种2-芳基丙酸(2-APA)类非甾体抗炎药(NSAID),以消旋体形式存在并被如此使用。尽管2-APA类药物的活性主要归因于其S-对映体,但氟比洛芬的药代动力学信息通常基于S-和R-氟比洛芬总浓度的测定。在本研究中,研究了氟比洛芬对映体单次给药后在人和大鼠体内的药代动力学。给雄性Sprague-Dawley大鼠静脉注射10mg/kg消旋氟比洛芬后,S-氟比洛芬的血浆浓度始终高于R-氟比洛芬(AUC = 134±39 vs 41±9mg·L-1·h)。在胆管插管大鼠中,胆汁排泄中结合型氟比洛芬占给药剂量的3.6-5.2%(S:R = 1.2-2.1)。给大鼠注射R-氟比洛芬后,在血浆中发现了两种对映体[AUC(R):AUC(S) = 0.10-0.16],表明对映体生物转化程度有限。这与先前报道的氟比洛芬在脂肪中的摄取程度有限一致。在健康志愿者中,口服100mg消旋剂量后,药物血浆浓度也观察到显著的立体选择性[AUC-(S):AUC(R) = 45.4±12.7:40.1±14.3mg·L-1·h]。与R-对映体相比,S-氟比洛芬的分布容积较小(7.23±1.9 vs 8.41±3.0L)和总清除率较低(1.23±0.34 vs 1.47±0.50L/h),但半衰期相等(4.21±1.2 vs 4.18±1.3h)。另一方面,在尿液中,R-构型占主导,因为在结合型氟比洛芬和一种未鉴定的代谢物中都发现了较多量的R-对映体。尿液中未检测到可忽略不计的完整氟比洛芬对映体。在人体中观察到的立体选择性不能归因于对映体生物转化,因为口服R-氟比洛芬后,在血浆和尿液中未检测到S-氟比洛芬。

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