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Use of a quadrupole linear ion trap mass spectrometer in metabolite identification and bioanalysis
Author(s) -
Xia YuanQing,
Miller Jeffrey D.,
Bakhtiar Ray,
Franklin Ronald B.,
Liu David Q.
Publication year - 2003
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.1037
Subject(s) - chemistry , quadrupole ion trap , ion trap , triple quadrupole mass spectrometer , mass spectrometry , selected reaction monitoring , ion , hybrid mass spectrometer , selected ion monitoring , analytical chemistry (journal) , quadrupole mass analyzer , top down proteomics , orbitrap , reproducibility , chromatography , tandem mass spectrometry , gas chromatography–mass spectrometry , organic chemistry
A new type of quadrupole linear ion trap mass spectrometer, Q TRAP™ LC/MS/MS system (Q TRAP™), was evaluated for its performance in two studies: firstly, the in vitro metabolism of gemfibrozil in human liver microsomes, and, secondly, the quantification of propranolol in rat plasma. With the built‐in information‐dependent‐acquisition (IDA) software, the instrument utilizes full scan MS in the ion trap mode and/or constant neutral loss scans as survey scans to trigger product ion scan (MS 2 ) and MS 3 experiments to obtain structural information of drug metabolites ‘on‐the‐fly’. Using this approach, five metabolites of gemfibrozil were detected in a single injection. This instrument combines some of the unique features of a triple quadrupole mass spectrometer, such as constant neutral loss scan, precursor ion scan and multiple reaction monitoring (MRM), together with the capability of a three‐dimensional ion trap. Therefore, it becomes a powerful instrument for metabolite identification. The fast duty cycle in the ion trap mode allows the use of full product ion scan for quantification. For the quantification of propranolol, both MRM mode and full product ion scan in the ion trap mode were employed. Similar sensitivity, reproducibility and linearity values were established using these two approaches. The use of the product ion scan mode for quantification provided a convenient tool in selecting transitions for improving selectivity during the method development stage. Copyright © 2003 John Wiley & Sons, Ltd.