Liquid chromatographic-mass spectrometric assay for quantitation of imatinib and its main metabolite (CGP 74588) in plasma

被引:96
作者
Parise, RA
Ramanathan, RK
Hayes, MJ
Egorin, MJ
机构
[1] Univ Pittsburgh, Program Mol Therapeut & Drug Discovery, Inst Canc, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Div Hematol Oncol, Dept Med, Sch Med, Pittsburgh, PA 15213 USA
[3] Novartis Inst Biomed Res, Dept Preclin Safety, E Hanover, NJ 07936 USA
[4] Univ Pittsburgh, Sch Med, Dept Pharmacol, Pittsburgh, PA 15213 USA
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2003年 / 791卷 / 1-2期
关键词
imatinib; CGP; 74588;
D O I
10.1016/S1570-0232(03)00206-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Imatinib mesylate (Gleevec, Glivec, ST1571) is a targeted, small molecule inhibitor of the oncogenes, BCR/ABL and c-KIT, and has striking antitumor activity in patients with chronic myelogenous leukemia or gastrointestinal stromal tumors. We have developed a liquid chromatographic-electrospray ionization mass spectrometric (LC-MS) method for quantifying imatinib and its main metabolite (CGP 74588) in plasma. The assay uses deuterated imatinib as the internal standard; acetonitrile deproteination; a Phenomenex Luna C-18(2) (5 mum, 50X4.6 nun) reversed-phase analytical column; a gradient mobile phase of 0.1% formic acid in methanol and water; and mass spectrometric detection using electrospray positive mode electron ionization. The assay has a lower limit of quantitation (LLOQ) of 30 ng/ml and is linear between 30 and 10 000 ng/ml for both imatinib and CGP 74588. We demonstrated the suitability of this assay for imatinib using it to quantify the concentrations of imatinib and CGP 74588 in plasma of a patient given a 200-mg dose of imatinib orally. We believe that this LC-MS assay should be an important tool for future pharmacokinetic studies of imatinib. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:39 / 44
页数:6
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