Determination of GDC-0449, a small-molecule inhibitor of the Hedgehog signaling pathway, in human plasma by solid phase extraction-liquid chromatographic-tandem mass spectrometry

被引:36
作者
Ding, X. [1 ]
Chou, B. [1 ]
Graham, R. A. [2 ]
Cheeti, S. [2 ]
Percey, S. [2 ]
Matassa, L. C. [3 ]
Reuschel, S. A. [3 ]
Meng, M. [3 ]
Liu, S. [3 ]
Voelker, T. [3 ]
Lum, B. L. [2 ]
Rudewicz, P. J. [1 ]
Hop, C. E. C. A. [1 ]
机构
[1] Genentech Inc, Drug Metab & Pharmacokinet, San Francisco, CA 94080 USA
[2] Genentech Inc, Dev Sci, Clin Pharmacokinet, San Francisco, CA 94080 USA
[3] Tandem Labs, Salt Lake City, UT 84124 USA
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2010年 / 878卷 / 9-10期
关键词
GDC-0449; Hedgehog pathway inhibitor; HPI; LC-MS/MS; 96-Well SPE; Human plasma;
D O I
10.1016/j.jchromb.2010.01.039
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
To support clinical development, a solid phase extraction (SPE) liquid chromatographic-tandem mass spectrometry (LC-MS/MS) method for the determination of GDC-0449 concentrations in human plasma has been developed and validated. Samples (200 mu l) were extracted using an Oasis MCX 10 mg 96-well SPE plate and the resulting extracts were analyzed using reverse-phase chromatography coupled with a turbo-ionspray interface. The method was validated over calibration curve range 5-5000 ng/mL. Quadratic regression and 1/x(2) weighing were used. Within-run relative standard deviation (%RSD) was within 10.1% and accuracy ranged from 88.6% to 109.0% of nominal. Between-run %RSD was within 8.6% and accuracy ranged from 92.4% to 105.3% of nominal. Extraction recovery of GDC-0449 was between 88.3% and 91.2% as assessed using quality control sample concentrations. GDC-0449 was stable in plasma for 315 days when stored at 70 C and stable in reconstituted sample extracts for 117 h when stored at room temperature. Quantitative matrix effect/ion suppression experiment was performed and no significant matrix ion suppression was observed. This assay allows for the determination of GDC-0449 plasma concentrations over a sufficient time period to determine pharmacokinetic parameters at relevant clinical doses. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:785 / 790
页数:6
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