Department of Pharmacological and Pharmaceutical Sciences, College of Pharmacy, University of Houston, 1441 Moursund Street, Houston, TX 77030, United States.
College of Traditional Chinese Medicine, Shenyang Pharmaceutical University, 103 Wenhua Street, Shenyang, Liaoning 110016, China.
J Pharm Biomed Anal. 2018 Jan 30;148:65-72. doi: 10.1016/j.jpba.2017.09.013. Epub 2017 Sep 11.
The purpose of this study was to develop and validate a robust and sensitive LC-MS/MS method for simultaneous determinations of various tyrosine kinase inhibitors (TKIs) in biological samples and to apply the method to their pharmacokinetic studies. Processed samples were injected into the UHPLC system coupled to an ESI-triple quadrupole mass spectrometer. The compounds were separated on an AcQuity UHPLC BEH C18 column (50mm×2.1mm ID, 1.7μm) using a gradient elution of acetonitrile/0.1% formic acid in water. The mass analysis was performed in an API 3200 Qtrap mass spectrometer via selective reaction monitoring operated under a positive scanning mode. The method was validated over a linear range of 3.13-800nM for erlotinib; 6.25-1600nM for sunitinib, pazopanib, and axitinib; and 12.5-3200nM for sorafenib, dasatinib, lapatinib, and nilotinib, respectively. The intra-day and inter-day precision were <16.7% for quality control samples of the analytes at the low concentration level and <13.7% for all other concentrations. The accuracy (bias) for all analytes at three different concentration levels ranged from -12.2% to 15.0%. The recovery, matrix effect, and stability were all in the range of acceptance. Only 10μl of blood were needed, demonstrating the method's high sensitivity. The presented method was shown to be suitable for the analysis of serial blood samples collected from each mouse in a pharmacokinetic study, after the oral administration of 11 TKIs (each at 1mg/kg) as a mixture.
本研究旨在开发和验证一种灵敏、稳健的 LC-MS/MS 方法,用于同时测定生物样品中的各种酪氨酸激酶抑制剂(TKI),并将该方法应用于它们的药代动力学研究。处理后的样品注入 UHPLC 系统,与 ESI-三重四极杆质谱仪相连。采用梯度洗脱的方式,在 AcQuity UHPLC BEH C18 柱(50mm×2.1mm ID,1.7μm)上分离各化合物,流动相为乙腈/水中 0.1%甲酸。在正扫描模式下,通过选择反应监测(SRM),在 API 3200 Qtrap 质谱仪上进行质量分析。该方法在以下线性范围内进行验证:厄洛替尼为 3.13-800nM;舒尼替尼、帕唑帕尼和阿昔替尼为 6.25-1600nM;索拉非尼、达沙替尼、拉帕替尼和尼洛替尼分别为 12.5-3200nM。对于低浓度水平的分析物质控样品,日内和日间精密度均<16.7%;所有其他浓度的精密度均<13.7%。在三个不同浓度水平下,所有分析物的准确度(偏差)均在-12.2%至 15.0%之间。回收率、基质效应和稳定性均在可接受范围内。该方法仅需 10μl 血液,显示出高灵敏度。该方法适用于在口服 11 种 TKI(每种 1mg/kg)混合物后,从药代动力学研究中每只小鼠采集的一系列血样的分析。