Data acquisition and data mining techniques for metabolite identification using LC coupled to high-resolution MS

被引:7
作者
Ma, Shuguang [1 ]
Chowdhury, Swapan K. [1 ]
机构
[1] Genentech Inc, Dept Drug Metab & Pharmacokinet, San Francisco, CA 94080 USA
关键词
TRAP/ORBITRAP MASS-SPECTROMETER; TRAPPED REACTIVE METABOLITES; THOROUGH BACKGROUND SUBTRACTION; COLLISION-INDUCED DISSOCIATION; LC/MS DATA APPLICATION; Q-TOF-MS; DRUG METABOLITES; BIOLOGICAL MATRICES; ISOTOPE-PATTERN; HIGH-THROUGHPUT;
D O I
10.4155/BIO.13.103
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Metabolite identification plays a pivotal role through all stages of drug discovery and development. The task of detecting and characterizing drug metabolites in complex biological matrices is very challenging, due in part to the co-existence of drug-related material with a large excess of endogenous material. Deciphering information on drug metabolites in these complex biological systems requires not only sophisticated LC-MS systems, but also software that can help differentiate drug-related compounds from endogenous material in the MS data. Fortunately, there have been considerable advances in high-resolution MS technologies with improved mass accuracy. The high resolution and mass accuracy capabilities have necessitated and augmented the development of integrated data acquisition methods, which have significantly facilitated metabolite detection and identification. In this review, we discuss various data-dependent and -independent acquisition methods in combination with accurate mass-based data mining tools for metabolite identification in drug discovery and development.
引用
收藏
页码:1285 / 1297
页数:13
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