Luethi Dino, Durmus Selvi, Schinkel Alfred H, Schellens Jan H M, Beijnen Jos H, Sparidans Rolf W
Utrecht University, Faculty of Science, Department of Pharmaceutical Sciences, Division of Pharmacoepidemiology and Clinical Pharmacology, Universiteitsweg 99, 3584 CG, Utrecht, The Netherlands.
Biomed Chromatogr. 2014 Oct;28(10):1366-70. doi: 10.1002/bmc.3176. Epub 2014 Mar 12.
Regorafenib has recently been approved for the treatment of colorectal cancer. A bioanalytical liquid chromatography-tandem mass spectrometric assay for this multikinase inhibitor was developed and validated in plasma. The concentration range of the assay was 25-25,000 ng/mL. Protein precipitation with acetonitrile was used as sample pre-treatment with sorafenib as internal standard. The extract was diluted with methanol (25%, v/v) and then injected onto the sub-2 µm particle, bridged ethylsilicia hybrid trifunctional bonded C18 column. Isocratic elution using 0.02% (v/v) formic acid in a methanol-water mixture was used. Compounds were monitored by a triple quadrupole mass spectrometer in the selected reaction monitoring mode after positive electrospray ionization. Double logarithmic calibration was used; within-day precisions, between-day precisions, and accuracies were 3.2-9.2, 4.1-12.3 and 94.8-103.0%, respectively. High drug stability was observed under all relevant storage conditions. The assay was used to measure drug concentrations in a pharmacokinetic study in wild-type FVB mice.
瑞戈非尼最近已被批准用于治疗结直肠癌。为此多激酶抑制剂开发了一种生物分析液相色谱 - 串联质谱法,并在血浆中进行了验证。该分析方法的浓度范围为25 - 25,000 ng/mL。以索拉非尼为内标,用乙腈进行蛋白沉淀作为样品预处理。提取物用甲醇(25%,v/v)稀释,然后注入粒径小于2 µm的桥接乙基硅杂化三官能键合C18柱。使用在甲醇 - 水混合物中含0.02%(v/v)甲酸的等度洗脱。在正电喷雾电离后,通过三重四极杆质谱仪在选择反应监测模式下监测化合物。采用双对数校准;日内精密度、日间精密度和准确度分别为3.2 - 9.2%、4.1 - 12.3%和94.8 - 103.0%。在所有相关储存条件下均观察到高药物稳定性。该分析方法用于在野生型FVB小鼠的药代动力学研究中测量药物浓度。