Polasek Thomas M, Miners John O
Flinders University and Flinders Medical Centre, Department of Clinical Pharmacology, Bedford Park, 5042, Adelaide, Australia.
Expert Opin Drug Metab Toxicol. 2007 Jun;3(3):321-9. doi: 10.1517/17425255.3.3.321.
Mechanism-based inactivation (MBI) of human drug-metabolising CYP enzymes is an important consideration in the preclinical ADME evaluation of new drug candidates. In this report, the in vitro approaches used to investigate MBI of CYP enzymes are described, with an emphasis on the characterisation required to assess potential drug-drug interactions. Recent disparities in MBI data between in vitro test systems are also reviewed, highlighting the limitations of Escherichia coli-expressed human recombinant CYP in the prediction of drug-drug interactions that arise via MBI.
基于机制的人类药物代谢CYP酶失活(MBI)是新药候选物临床前ADME评估中的一个重要考虑因素。在本报告中,描述了用于研究CYP酶MBI的体外方法,重点是评估潜在药物相互作用所需的特征描述。还回顾了体外测试系统之间MBI数据最近的差异,突出了大肠杆菌表达的人重组CYP在预测通过MBI产生的药物相互作用方面的局限性。