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
相关论文
共 50 条
  • [1] In vitro assessment of antitumor activities of the PI3K/mTOR inhibitor GSK2126458
    Albawardi, Alia
    Al Ayyan, Muna
    Al Bashir, Mohamed
    Souid, Abdul-Kader
    Almarzooqi, Saeeda
    CANCER CELL INTERNATIONAL, 2014, 14
  • [2] In vitro assessment of antitumor activities of the PI3K/mTOR inhibitor GSK2126458
    Alia Albawardi
    Muna Al Ayyan
    Mohamed Al Bashir
    Abdul-Kader Souid
    Saeeda Almarzooqi
    Cancer Cell International, 14
  • [3] The Pi3K inhibitor GSK2126458 is highly toxic in ovarian dysgerminoma
    Almarzooqi, Saeeda
    Albawardi, Alia
    Souid, Abdul-Kader
    CLINICAL CANCER RESEARCH, 2012, 18 (10)
  • [4] [11C]GSK2126458 and [18F]GSK2126458 as new PET agents for imaging of PI3K and mTOR in cancer
    Wang, Min
    Gao, Mingzhang
    Miller, Kathy
    Zheng, Qi-Huang
    JOURNAL OF NUCLEAR MEDICINE, 2012, 53
  • [5] Liquid chromatography-tandem mass spectrometric assay for the ALK inhibitor crizotinib in mouse plasma
    Sparidans, Rolf W.
    Tang, Seng Chuan
    Nguyen, Luan N.
    Schinkel, Alfred H.
    Schellens, Jan H. M.
    Beijnen, Jos H.
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2012, 905 : 150 - 154
  • [6] The Pi3K inhibitor GSK2126458 is highly toxic in breast ductal carcinoma
    Albawardi, Alia
    Almarzooqi, Saeeda
    Al Bashir, Mohamed
    Souid, Abdul-Kader
    CLINICAL CANCER RESEARCH, 2012, 18 (10)
  • [7] Discovery of GSK2126458, a Highly Potent Inhibitor of PI3K and the Mammalian Target of Rapamycin
    Knight, Steven D.
    Adams, Nicholas D.
    Burgess, JoeIle L.
    Chaudhari, Amita M.
    Darcy, Michael G.
    Donatelli, Carla A.
    Luengo, Juan I.
    Newlander, Ken A.
    Parrish, Cynthia A.
    Ridgers, Lance H.
    Sarpong, Martha A.
    Schmidt, Stanley J.
    Van Aller, Glenn S.
    Carson, Jeffrey D.
    Diamond, Melody A.
    Elkins, Patricia A.
    Gardiner, Christine M.
    Garver, Eric
    Gilbert, Seth A.
    Gontarek, Richard R.
    Jackson, Jeffrey R.
    Kershner, Kevin L.
    Luo, Lusong
    Raha, Kaushik
    Sherk, Christian S.
    Sung, Chiu-Mei
    Sutton, David
    Tummino, Peter J.
    Wegrzyn, Ronald J.
    Auger, Kurt R.
    Dhanak, Dashyant
    ACS MEDICINAL CHEMISTRY LETTERS, 2010, 1 (01): : 39 - 43
  • [8] Liquid chromatography-tandem mass spectrometric assay for the mutated BRAF inhibitor dabrafenib in mouse plasma
    Sparidans, Rolf W.
    Durmus, Selvi
    Schinkel, Alfred H.
    Schellens, Jan H. M.
    Beijnen, Jos H.
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2013, 925 : 124 - 128
  • [9] Liquid chromatography-tandem mass spectrometric assay for the multikinase inhibitor regorafenib in plasma
    Luethi, Dino
    Durmus, Selvi
    Schinkel, Alfred H.
    Schellens, Jan H. M.
    Beijnen, Jos H.
    Sparidans, Rolf W.
    BIOMEDICAL CHROMATOGRAPHY, 2014, 28 (10) : 1366 - 1370
  • [10] Liquid chromatography-tandem mass spectrometric assay for the PARP inhibitor rucaparib in plasma
    Sparidans, Rolf W.
    Durmus, Selvi
    Schinkel, Alfred H.
    Schellens, Jan H. M.
    Beijnen, Jos H.
    JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2014, 88 : 626 - 629