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超高效液相色谱-串联质谱法测定大鼠血浆中扁蓄苷及其在药代动力学研究中的应用

UPLC-MS/MS method for determination of avicularin in rat plasma and its application to a pharmacokinetic study.

作者信息

Zhang Wei-Min, Li Rui-Fang, Sun Ming, Hu Da-Ming, Qiu Jian-Fei, Yan Yun-Hao

机构信息

The First Affiliated Hospital of Henan University of Science and Technology, Luoyang, Henan 471003, PR China.

Medical College of Henan University of Science and Technology, Luoyang, Henan 471003, PR China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2014 Aug 15;965:107-11. doi: 10.1016/j.jchromb.2014.06.015. Epub 2014 Jun 20.

Abstract

A rapid, sensitive and selective ultra-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS) was developed and validated for the determination and pharmacokinetic investigation of avicularin in rat plasma. Sample preparation was accomplished through a simple one-step deproteinization procedure with 0.2 mL of acetonitrile-methanol (9:1, v/v) to a 0.1 mL plasma sample. Plasma samples were separated by UPLC on an Acquity UPLC BEH C18 column using a mobile phase consisting of acetonitrile-0.1% formic acid in water with gradient elution. The total run time was 1.60 min and the elution of avicularin was at 1.20 min. The detection was performed on a triple quadrupole tandem mass spectrometer in the multiple reaction-monitoring (MRM) mode using the respective transitions m/z 434.1→301.3 for avicularin and m/z 237.2→194.3 for carbamazepine (IS), respectively. The calibration curve was linear over the range of 10-3000 ng/mL with a lower limit of quantitation (LLOQ) of 10 ng/mL. Mean recovery of avicularin in plasma was in the range of 84.2-89.5%. Intra-day and inter-day precision were both <12%. This method was successfully applied in pharmacokinetic study after intravenous administration of 5.0mg/kg avicularin in rats.

摘要

建立了一种快速、灵敏且选择性高的超高效液相色谱串联质谱法(UPLC-MS/MS),用于测定大鼠血浆中扁蓄苷并进行药代动力学研究。通过向0.1 mL血浆样品中加入0.2 mL乙腈-甲醇(9:1,v/v)进行简单的一步脱蛋白程序来完成样品制备。血浆样品在Acquity UPLC BEH C18柱上通过UPLC分离,流动相由乙腈-0.1%甲酸水溶液组成并进行梯度洗脱。总运行时间为1.60分钟,扁蓄苷在1.20分钟洗脱。在三重四极杆串联质谱仪上采用多反应监测(MRM)模式进行检测,扁蓄苷的相应跃迁为m/z 434.1→301.3,卡马西平(内标物,IS)的跃迁为m/z 237.2→194.3。校准曲线在10 - 3000 ng/mL范围内呈线性,定量下限(LLOQ)为10 ng/mL。扁蓄苷在血浆中的平均回收率在84.2 - 89.5%范围内。日内和日间精密度均<12%。该方法成功应用于大鼠静脉注射5.0mg/kg扁蓄苷后的药代动力学研究。

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