4.6 Article

Detailed study of imatinib metabolization using high-resolution mass spectrometry

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1409, Issue -, Pages 173-181

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2015.07.033

Keywords

Drug metabolization; Tyrosine kinase inhibitor; Orbital ion trap; Fragmentation; Exact mass

Funding

  1. Internal Grant Agency of Ministry of Health, Czech Republic [NT12218-4/2011]
  2. European Social Fund [CZ.1.07/2.3.00/30.0004]
  3. Ministry of Education, Youth and Sports [MSMT-7778/2014, LO1304]

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Modern high resolution mass spectrometry offers unique identification capability in drug metabolism studies. In this work detailed imatinib metabolization in the plasma of patients with chronic myeloid leukemia is presented. The metabolites were separated by liquid chromatography on a C18 column with mass spectrometry detection via an Orbitrap Elite instrument (Thermo Scientific) based on exact mass measurement. A scan range of m/z 350-1200 resolution of 60,000 was applied (mass accuracy of 5 ppm). The data were evaluated using the advanced software for mass spectrometry Mass Frontier and Met-Works. In all plasma samples, studied 90 metabolites in the concentration range of 0.0001-1 mu mol/L were identified by m/z values and confirmed by exact mass measurement of the MS2 and MS3 fragmentations. In order to achieve optimal clinical response and avoid toxicity, current therapeutic monitoring of parent drug is a useful tool for the individualization of treatment. Current high-resolution mass spectrometry possesses the potential to broaden this approach by monitoring number of potentially clinically relevant drug metabolites. (C) 2015 Elsevier B.V. All rights reserved.

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