A routine feasible HPLC analysis for the anti-angiogenic tyrosine kinase inhibitor, sunitinib, and its main metabolite, SU12662, in plasma

被引:35
|
作者
Etienne-Grimaldi, Marie-Christine [1 ]
Renee, Nicole [1 ]
Izzedine, Hassan [2 ]
Milano, Gerard [1 ]
机构
[1] Ctr Antoine Lacassagne, Oncopharmacol Unit, F-06189 Nice 2, France
[2] Hop La Pitie Salpetriere, Dept Med Oncol, Paris, France
关键词
Sunitinib; HPLC; Pharmacokinetics; ENDOTHELIAL GROWTH-FACTOR; ANTITUMOR-ACTIVITY; SU11248; RECEPTOR; MALATE;
D O I
10.1016/j.jchromb.2009.09.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Sunitinib is an oral inhibitor of multiple tyrosine kinase receptors with antitumor activity in metastatic renal cell carcinoma. SO far, published methods for analysis of sunitinib and its active metabolite (SUI 2662) in plasma are exclusively based on mass spectrometry. In the context of a large-scale feasibility pharmacokinetic analysis, we developed an original, simple, high-performance liquid chromatography (HPLC) assay with UV detection. A stability Study Of sunitinib and SU12662 in different light exposure conditions is presented. Due to photo-instability of the Compounds, blood sampling and the whole handling procedure have to be performed quickly and with minimal light exposure (6-7 lx). Following single organic extraction with tert-butyl methyl ether, HPLC analysis was performed on an ODS Column and UV detection was monitored at 369 nm (run time 15 min). This assay was selective and sensitive enough (limit of detection approximately 1 ng/ml) to quantify minimal concentrations at steady state (Css min) of sunitinib and SU12662 in treated patients. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:3757 / 3761
页数:5
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