Advances in mass spectrometry applied to pharmaceutical metabolomics

被引:51
|
作者
Drexler, Dieter M. [1 ]
Reily, Michael D. [2 ]
Shipkova, Petia A. [3 ]
机构
[1] Bristol Myers Squibb Co, Res & Dev Discovery Analyt Sci, Wallingford, CT 06492 USA
[2] Bristol Myers Squibb Co, Res & Dev Discovery Analyt Sci, Princeton, NJ 08543 USA
[3] Bristol Myers Squibb Co, Res & Dev Discovery Analyt Sci, Pennington, NJ 08534 USA
关键词
Metabolomics; Metabonomics; Mass spectrometry; PERFORMANCE LIQUID-CHROMATOGRAPHY; HIGH-THROUGHPUT; GAS-CHROMATOGRAPHY; SYSTEMS BIOLOGY; TARGETED METABOLOMICS; DRUG DEVELOPMENT; INBORN-ERRORS; TOF-MS; METABONOMICS; IDENTIFICATION;
D O I
10.1007/s00216-010-4370-8
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Metabolomics, also referred to in the literature as metabonomics, is a relatively new systems biology tool for drug discovery and development and is increasingly being used to obtain a detailed picture of a drug's effect on the body. Metabolomics is the qualitative assessment and relative or absolute quantitative measurement of the endogenous metabolome, defined as the complement of all native small molecules (metabolites less than 1,500 Da). A metabolomics study frequently involves the comparative analysis of sample sets from a normal state and a perturbed state, where the perturbation can be of any nature, such as genetic knockout, administration of a drug, or change in diet or lifestyle. Advances in mass spectrometry (MS) technologies including direct introduction or in-line chromatographic separation modes, ionization techniques, mass analyzers, and detection methods have provided powerful tools to assess the molecular changes in the metabolome. This review focuses on advances in MS pertaining to the analytical data generation for the main metabolomics methods, namely, fingerprinting, nontargeted, and targeted approaches, as they are applied to pharmaceutical drug discovery and development.
引用
收藏
页码:2645 / 2653
页数:9
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