Liu Zhi-hao, Liu Ke-xin
Department of Clinical Pharmacology, College ofPharmacy, Dalian Medical University, Dalian 116044, China.
Yao Xue Xue Bao. 2011 Apr;46(4):370-6.
The absorption of oral drug in the intestine is an important factor to determine the drug bioavailability. There are many intestinal transporters mediating drug absorption, distribution, excretion and drug-drug interaction. Understanding the transport mechanism can improve the effectiveness and safety of drug and guide clinical rational use of drugs. The in vivo and in vitro methods are used to predict the transport mechanism of drugs by intestinal transporters in the intestine. The purposes of this article are to introduce the main transporters in the intestinal tract, to explain the transport mechanism and to summarize the advantages and disadvantages of the research methods of them.
口服药物在肠道中的吸收是决定药物生物利用度的一个重要因素。有许多肠道转运体介导药物的吸收、分布、排泄以及药物-药物相互作用。了解转运机制可以提高药物的有效性和安全性,并指导临床合理用药。体内和体外方法被用于预测肠道中药物经肠道转运体的转运机制。本文的目的是介绍肠道中的主要转运体,解释其转运机制,并总结研究这些转运体方法的优缺点。