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巴米品在大鼠体内的生物转化与药代动力学。2. 药代动力学研究(1.)

[Biotransformation and pharmacokinetics of bamipine in rats. 2. Studies of the pharmacokinetics (1.)].

作者信息

Neidlein V R, Kleiser M

出版信息

Arzneimittelforschung. 1987 Feb;37(2):174-7.

PMID:2883979
Abstract

Biotransformation and Pharmacokinetics of Bamipine in Rats/2nd Communication: Pharmacokinetic studies (Part I). After oral application in Wistar rats the pharmacokinetic properties of N-phenyl-N-benzyl-4-amino-1-methylpiperidine (bamipine) were investigated. The compound is quantitatively absorbed. Bamipine distribution occurs in the whole organism. A transient accumulation was found in liver, kidney, spleen and lung. The compound's liquor patency was established. The elimination is mainly renal (85.81%), 13.23% are eliminated by feces. The total excretion after 96 h is more than 99%.

摘要

巴米品在大鼠体内的生物转化及药代动力学/第二次通讯:药代动力学研究(第一部分)。在Wistar大鼠口服给药后,对N-苯基-N-苄基-4-氨基-1-甲基哌啶(巴米品)的药代动力学特性进行了研究。该化合物能被定量吸收。巴米品分布于整个机体。在肝脏、肾脏、脾脏和肺中发现有短暂蓄积。确定了该化合物的血脑通透性。消除主要通过肾脏(85.81%),13.23%通过粪便排出。96小时后的总排泄率超过99%。

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