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离子对形成对药物药代动力学性质的影响。第5部分:离子对形成对大鼠体内溴苄铵和己基水杨酸消除的影响。

Influence of the ion-pair-formation on the pharmacokinetic properties of drugs. Part 5: Influence of ion-pair-formation on elimination of bretylium and hexylsalicylic acid in rats.

作者信息

Neubert R, Hause C, Härtl A, Amlacher R

机构信息

Sektion Pharmazie der Martin-Luther-Universität Halle, Jena.

出版信息

Pharmazie. 1989 Sep;44(9):630-1.

PMID:2608709
Abstract

Following i.v. administration of the hydrophilic drug bretylium (1) and the lipophilic hexylsalicylic acid (2) in rats the plasma levels of 2 were increased due to an increased intestinal reabsorption of 2. Under these conditions the biliary eliminated amount of 2 was 8 times higher than that following the administration of 2 alone. The eneteroheptic circulation of 2 was found to be interrupted following i.v. administration of 1 and 2 and additional oral administration of an anionic exchanger. Then the plasma levels of 2 were not influenced by 1. On other hand the plasma levels of 2 appear to be too low in order to influence those of 1.

摘要

在大鼠静脉注射亲水性药物溴苄铵(1)和亲脂性己基水杨酸(2)后,由于2的肠道重吸收增加,2的血浆水平升高。在这些条件下,2经胆汁消除的量比单独给予2时高8倍。静脉注射1和2并额外口服阴离子交换剂后,发现2的肠肝循环被中断。此时,2的血浆水平不受1的影响。另一方面,2的血浆水平似乎过低,无法影响1的血浆水平。

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