MSM, an Efficient Workflow for Metabolite Identification Using Hybrid Linear Ion Trap Orbitrap Mass Spectrometer

被引:17
作者
Cho, Robert [1 ]
Huang, Yingying [2 ]
Schwartz, Jae C. [2 ]
Chen, Yan [2 ]
Carlson, Timothy J. [1 ]
Ma, Ji [1 ]
机构
[1] Amgen Inc, Dept Pharmacokinet & Drug Metab, San Francisco, CA 94080 USA
[2] Thermo Fisher Sci, San Jose, CA 95134 USA
关键词
MSM; Wide isolation width HCD MS2; Accurate mass filter; Orbitrap; Metabolite identification; LC-MS; PHASE-II METABOLITES; DRUG DISCOVERY; VERAPAMIL; RAT; PHARMACOKINETICS; INSTRUMENTATION; REGIOCHEMISTRY; CULTURES;
D O I
10.1007/s13361-012-0351-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Identification of drug metabolites can often yield important information regarding clearance mechanism, pharmacologic activity, or toxicity for drug candidate molecules. Additionally, the identification of metabolites can provide beneficial structure-activity insight to help guide lead optimization efforts towards molecules with optimal metabolic profiles. There are challenges associated with detecting and identifying metabolites in the presence of complex biological matrices, and new LC-MS technologies have been developed to meet these challenges. In this report, we describe the development of an experimental approach that applies unique features of the hybrid linear ion trap Orbitrap mass spectrometer to streamline in vitro and in vivo metabolite identification experiments. The approach, referred to as MSM, utilizes multiple collision cells, dissociation methods, mass analyzers, and detectors. With multiple scan types and different dissociation modes built into one experimental method, along with flexible post-acquisition analysis options, the MSM workflow offers an attractive option to fast and reliable identification of metabolites in different kinds of in vitro and in vivo samples. The MSM workflow was successfully applied to metabolite identification analysis of verapamil in both in vitro rat hepatocyte incubations and in vivo rat bile samples.
引用
收藏
页码:880 / 888
页数:9
相关论文
共 28 条
[1]   MSE with mass defect filtering for in vitro and in vivo metabolite identification [J].
Bateman, Kevin P. ;
Castro-Perez, Jose ;
Wrona, Mark ;
Shockcor, John P. ;
Yu, Kate ;
Oballa, Renata ;
Nicoll-Griffith, Deborah A. .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2007, 21 (09) :1485-1496
[2]   Quantitative-Qualitative Data Acquisition Using a Benchtop Orbitrap Mass Spectrometer [J].
Bateman, Kevin P. ;
Kellmann, Markus ;
Muenster, Helmut ;
Papp, Robert ;
Taylor, Lester .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2009, 20 (08) :1441-1450
[3]   Metabolism of verapamil in cultures of rat alveolar epithelial cells and pharmacokinetics after administration by intravenous and inhalation routes [J].
Borlak, J ;
Blickwede, M ;
Hansen, T ;
Koch, W ;
Walles, M ;
Levsen, K .
DRUG METABOLISM AND DISPOSITION, 2005, 33 (08) :1108-1114
[4]  
EICHELBAUM M, 1979, DRUG METAB DISPOS, V7, P145
[5]  
Food and Drug Administration Center for Drug Evaluation and Research (CDER), 2008, GUID IND SAF TEST DR
[6]   Role of pharmacologically active metabolites in drug discovery and development [J].
Fura, A .
DRUG DISCOVERY TODAY, 2006, 11 (3-4) :133-142
[7]  
Gibson G.G., 1986, INTRO DRUG METABOLIS, DOI [10.1007/978-1-4899-3188-7, DOI 10.1007/978-1-4899-3188-7, 10.1007/978-1-4899-3188-7.]
[8]   Cytochrome P450s and other enzymes in drug metabolism and toxicity [J].
Guengerich, FP .
AAPS JOURNAL, 2006, 8 (01) :E101-E111
[9]   Common and uncommon cytochrome P450 reactions related to metabolism and chemical toxicity [J].
Guengerich, FP .
CHEMICAL RESEARCH IN TOXICOLOGY, 2001, 14 (06) :611-650
[10]   Structure elucidation of phase II metabolites by tandem mass spectrometry:: an overview [J].
Levsen, K ;
Schiebel, HM ;
Behnke, B ;
Dötzer, R ;
Dreher, W ;
Elend, M ;
Thiele, H .
JOURNAL OF CHROMATOGRAPHY A, 2005, 1067 (1-2) :55-72