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一种用于测定大鼠血浆中曲格列汀的快速灵敏的超高效液相色谱-串联质谱法及其在药代动力学研究中的应用。

A rapid and sensitive UHPLC-MS/MS assay for the determination of trelagliptin in rat plasma and its application to a pharmacokinetic study.

作者信息

Hu Xiao-Xia, Lan Tian, Chen Zhe, Yang Cheng-Cheng, Tang Peng-Fei, Yuan Ling-Jing, Hu Guo-Xin, Cai Jian-Ping

机构信息

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.

出版信息

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.

Abstract

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.

摘要

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。

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