Validated bioanalytical method for the quantification of RGB-286638, a novel multi-targeted protein kinase inhibitor, in human plasma and urine by liquid chromatography/tandem triple-quadrupole mass spectrometry

被引:11
作者
de Bruijn, Peter [1 ]
Moghaddam-Helmantel, Inge M. Ghobadi [1 ]
de Jonge, Maja J. A. [1 ]
Meyer, Thorsten [2 ]
Lam, Mei-Ho [1 ]
Verweij, Jaap [1 ]
Wiemer, Erik A. C. [1 ]
Loos, Walter J. [1 ]
机构
[1] Univ Med Ctr, Dept Med Oncol, Erasmus MC Daniel Hoed Canc Ctr, NL-3075 EA Rotterdam, Netherlands
[2] GPC Biotech AG, Martinsried, Germany
关键词
RGB-286638; Human; Plasma; Urine; Validated; LC-MS/MS; CANCER;
D O I
10.1016/j.jpba.2009.06.048
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A rapid and sensitive liquid chromatography/tandem mass spectrometry (LC-MS/MS) method has been developed and validated for the quantitative determination of RBG-286638, a novel multi-targeted protein kinase inhibitor, in 200 mu l aliquots of human potassium EDTA plasma with deuterated RGB-286638 as internal standard. The sample extraction and cleaning-up involved a simple liquid-liquid extraction with 100 mu l aliquots of acetonitrile and 1 ml aliquots of n-butylchloride. Urine was accurately 5- and 10-fold diluted in blank plasma prior to extraction. Chromatographic separations were achieved on a reversed phase C-18 column eluted at a flow-rate of 0.250 ml/min on a gradient of 0.2 mM ammonium formate and acetonitrile both acidified with 0.1% formic acid. The overall cycle time of the method was 7 min, with RGB-286638 eluting at 1.9 min. The multiple reaction monitoring transitions were set at 546 > 402 (m/z), and 549 > 402 (m/z) for RGB-286638 and the internal standard, respectively. The calibration curves were linear over the range of 2.00 to 1000 ng/ml with the lower limit of quantitation validated at 2.00 ng/ml. The within-run and between-run precisions were within 7.90%, while the accuracy ranged from 92.2% to 99.7%. The method was successfully applied to samples derived from a clinical study. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:977 / 982
页数:6
相关论文
共 12 条
[1]   Countering matrix effects in environmental liquid chromatography-electrospray ionization tandem mass spectrometry water analysis for endocrine disrupting chemicals [J].
Benijts, T ;
Dams, R ;
Lambert, W ;
De Leenheer, A .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1029 (1-2) :153-159
[2]  
CALIGIURI M, 2006, 97 ANN M AM ASS CANC
[3]  
CALIGIURI M, 2008, 20 EORTC NCI AACR S
[4]  
CIRSTEA D, 2008, 50 AM SOC HEM ASH AN
[5]   Mammalian cyclin-dependent kinases [J].
Malumbres, M ;
Barbacid, M .
TRENDS IN BIOCHEMICAL SCIENCES, 2005, 30 (11) :630-641
[6]   CDK inhibitors in cancer therapy: what is next? [J].
Malumbres, Marcos ;
Pevarello, Paolo ;
Barbacid, Mariano ;
Bischoff, James R. .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2008, 29 (01) :16-21
[7]   Cell cycle kinases in cancer [J].
Malumbres, Marcos ;
Barbacid, Mariano .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2007, 17 (01) :60-65
[8]   Strategies for the assessment of matrix effect in quantitative bioanalytical methods based on HPLC-MS/MS [J].
Matuszewski, BK ;
Constanzer, ML ;
Chavez-Eng, CM .
ANALYTICAL CHEMISTRY, 2003, 75 (13) :3019-3030
[9]   Cyclin-dependent kinase pathways as targets for cancer treatment [J].
Shapiro, GI .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (11) :1770-1783
[10]   Cancer cell cycles [J].
Sherr, CJ .
SCIENCE, 1996, 274 (5293) :1672-1677