Detecting and characterizing reactive metabolites by liquid chromatography/tandem mass spectrometry

被引:126
|
作者
Ma, Shuguang [1 ]
Subramanian, Raju [1 ]
机构
[1] Amgen Inc, Pharmacokinet & Drug Metab, Thousand Oaks, CA 91320 USA
来源
JOURNAL OF MASS SPECTROMETRY | 2006年 / 41卷 / 09期
关键词
bioactivation; reactive metabolite; glutathione; acyl glucuronide; acyl coenzyme A thioester; covalent drug-protein adduct; mass spectrometry; LC-MS/MS;
D O I
10.1002/jms.1098
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Metabolic activation of a drug leading to reactive metabolite(s) that can covalently modify proteins is considened an initial step that may lead to drug-induced organ toxicities. Characterization of reactive metaboliles is critical to designing new drug candidates with an improved toxicological profile. High performance liquid chromatography (HPLC) coupled with mass spectrometry (MS) predominates over all analytical tools used for screening and characterization of reactive metabolites. In this review, a brief description of experimental approaches employed for assessing reactive metabolites is followed by a discussion on the reactivity of acyl glucuronides and acyl coenzyme A thioesters. Techniques for high-throughput screening and quantitation of reactive metabolite formation are also described, along with proteomic approaches used to identify protein targets and modification sites by reactive metabolites. Strategies for dealing with reactive metabolites are reviewed. In conclusion, we discuss the challenges and future fields in this field of research. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:1121 / 1139
页数:19
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