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P-糖蛋白在药代动力学药物-药物相互作用中的作用。

The contribution of P-glycoprotein to pharmacokinetic drug-drug interactions.

作者信息

Yu D K

机构信息

Quintiles, Inc., Kansas City, Missouri, USA.

出版信息

J Clin Pharmacol. 1999 Dec;39(12):1203-11. doi: 10.1177/00912709922012006.

Abstract

P-glycoprotein (PGP) is well known because of its contribution to multiple-drug resistance during anticancer treatment. More recent work indicates that PGP mediates the transcellular transport of many drugs in addition to anticancer compounds. Because of this reason, its potential role in clinically significant drug-drug interactions has just begun to be realized. This article provides an overview of published in vitro, in situ, and in vivo drug-drug interaction results that are related to PGP transport so that the awareness of the scientific community can be heightened. In addition, several recommendations are made to take full advantage of the recently published data.

摘要

P-糖蛋白(PGP)因其在抗癌治疗期间对多药耐药性的作用而广为人知。最近的研究表明,PGP除了介导抗癌化合物外,还介导许多药物的跨细胞转运。因此,其在临床上显著的药物相互作用中的潜在作用才刚刚开始被认识到。本文概述了已发表的与PGP转运相关的体外、原位和体内药物相互作用结果,以提高科学界的认识。此外,还提出了一些建议,以充分利用最近发表的数据。

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