Etienne-Grimaldi Marie-Christine, Renée Nicole, Izzedine Hassan, Milano Gérard
Oncopharmacology Unit, Centre Antoine Lacassagne, 33 Avenue de Valombrose, 06189 Nice Cedex 2, France.
J Chromatogr B Analyt Technol Biomed Life Sci. 2009 Nov 1;877(29):3757-61. doi: 10.1016/j.jchromb.2009.09.011. Epub 2009 Sep 17.
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 (SU12662) 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.
舒尼替尼是一种口服的多酪氨酸激酶受体抑制剂,对转移性肾细胞癌具有抗肿瘤活性。到目前为止,已发表的血浆中舒尼替尼及其活性代谢物(SU12662)的分析方法均仅基于质谱法。在大规模可行性药代动力学分析的背景下,我们开发了一种原创的、简单的、具有紫外检测的高效液相色谱(HPLC)测定法。本文介绍了舒尼替尼和SU12662在不同光照条件下的稳定性研究。由于这些化合物的光不稳定性,必须快速进行血样采集和整个处理过程,且光照最少(6 - 7勒克斯)。用叔丁基甲基醚进行单次有机萃取后,在ODS柱上进行HPLC分析,并在369 nm处监测紫外检测(运行时间15分钟)。该测定法具有足够的选择性和灵敏度(检测限约为1 ng/ml),能够定量治疗患者中舒尼替尼和SU12662稳态时的最低浓度(Css min)。