Liquid chromatography-tandem mass spectrometric assay for the PI3K/mTOR inhibitor GSK2126458 in mouse plasma and tumor homogenate

被引:4
|
作者
Dolman, M. Emmy M. [1 ]
Westerhout, Ellen M. [1 ]
Hamdi, Mohamed [1 ]
Schellens, Jan H. M. [2 ,3 ]
Beijnen, Jos H. [2 ,3 ,4 ]
Sparidans, Rolf W. [2 ]
机构
[1] Univ Amsterdam, Dept Oncogen, Amsterdam Med Ctr, NL-1105 AZ Amsterdam, Netherlands
[2] Univ Utrecht, Fac Sci, Dept Pharmaceut Sci, Div Pharmacoepidemiol & Clin Pharmacol, NL-3584 CG Utrecht, Netherlands
[3] Netherlands Canc Inst, Dept Clin Pharmacol, NL-1066 CX Amsterdam, Netherlands
[4] Slotervaart Hosp, Dept Pharm & Pharmacol, NL-1066 EC Amsterdam, Netherlands
关键词
GSK2126458; LC-MS/MS; Mouse; Plasma; Tumor homogenate; TARGET;
D O I
10.1016/j.jpba.2015.01.026
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A quantitative bioanalytical liquid chromatography-tandem mass spectrometric (LC-MS/MS) assay for GSK2126458, a dual PI3K/mTOR inhibitor, was developed and validated. Plasma and tumor homogenate samples were pre-treated using protein precipitation with acetonitrile containing dabrafenib as internal standard. After dilution with water, the extract was directly injected into the reversed-phase liquid chromatographic system. The eluate was transferred into the electrospray interface with positive ionization and compounds were detected in the selected reaction monitoring mode of a triple quadrupole mass spectrometer. The assay was completely validated for plasma in a 4-4000 ng/ml calibration range with r(2) = 0.9996 +/- 0.0003 using double logarithmic calibration (n = 5). Within-run precisions (n = 6) were 2.0-5.3% and between-run (3 runs; n =18) precisions 2.7-5.8%. Accuracies were between 101 and 105% for the whole calibration range. The drug was sufficiently stable under all relevant analytical conditions. Finally, the assay was successfully applied to determine plasma and tumor drug levels after oral administration of GSK2126458 to mice with AMC711T neuroblastoma xenografts. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:403 / 408
页数:6
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