Hu Xiao-Xia, Lan Tian, Chen Zhe, Yang Cheng-Cheng, Tang Peng-Fei, Yuan Ling-Jing, Hu Guo-Xin, Cai Jian-Ping
Department of Pharmacology, School of Pharmacy of Wenzhou Medical University, Wenzhou, Zhejiang, China.
Department of Pharmacology, School of Pharmacy of Wenzhou Medical University, Wenzhou, Zhejiang, China.
J Chromatogr B Analyt Technol Biomed Life Sci. 2016 Oct 15;1033-1034:166-171. doi: 10.1016/j.jchromb.2016.08.024. Epub 2016 Aug 16.
This study aims to develop and validate a simple, rapid and sensitive ultra-performance liquid chromatography with tandem mass spectrometry (UHPLC-MS/MS) method for exploring pharmacokinetic characteristics of trelagliptin. Protein precipitation by acetonitrile was used to prepare plasma sample. A RRHD Eclipse Plus C18 (2.1×50mm, 1.8μ) column with gradient mobile phase (containing acetonitrile and 0.1% formic acid) help to achieve the separation of trelagliptin and carbamazepine (IS) with high selectivity. Detection of target fragment ions m/z 358.2→133.9 for trelagliptin, and m/z 237.1→194.0 for IS was performed in positive-ion electrospray ionization mass spectrometry by multiple reaction monitoring. Linear calibration plots were achieved in the range of 5-4000ng/mL for trelagliptin (R(2)=0.999) in rat plasma. The recovery of trelagliptin ranged from 87.8% to 93.7%. The method was showed to be accurate, precise and stable. No obvious matrix effect was found. It has been fully validated and successfully applied to pharmacokinetic study of trelagliptin.
本研究旨在开发并验证一种简单、快速且灵敏的超高效液相色谱-串联质谱法(UHPLC-MS/MS),用于探究曲格列汀的药代动力学特征。采用乙腈沉淀蛋白法制备血浆样本。使用RRHD Eclipse Plus C18(2.1×50mm,1.8μ)色谱柱,以含乙腈和0.1%甲酸的梯度流动相,有助于高选择性地分离曲格列汀和卡马西平(内标)。在正离子电喷雾电离质谱中,通过多反应监测对曲格列汀的目标碎片离子m/z 358.2→133.9以及内标的目标碎片离子m/z 237.1→194.0进行检测。曲格列汀在大鼠血浆中的线性校准曲线在5-4000ng/mL范围内获得(R(2)=0.999)。曲格列汀的回收率在87.8%至93.7%之间。该方法经证明准确、精密且稳定。未发现明显的基质效应。该方法已得到充分验证,并成功应用于曲格列汀的药代动力学研究。