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UHPLC-MS simultaneous determination and pharmacokinetic study of three aromatic acids and one monoterpene in rat plasma after oral administration of shaofu zhuyu decoction

机译:少付逐瘀汤口服液中UHPLC-MS同时测定大鼠血浆中三种芳香酸和一种单萜的药动学

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摘要

We developed a sensitive and rapid method for determination of ferulic acid, caffeic acid, vanillic acid, and paeoniflorin in rat plasma based on ultra high performance liquid chromatography coupled with tandem mass spectrometry (UHPLC-MS/MS). The separation of the four compounds was carried out on an AcQuity UHPLC? BEH C18 column using a mobile phase consisting of acetonitrile and water (containing 0.1% formic acid). Electrospray ionization in positive and negative ion mode and multiple reaction monitoring was used to identify and quantify active components. All calibration curves gave good linearity (r 0.991) over the concentration range from 4.24-2875 ngmL -1 for all components. The precision of the in vivo study was evaluated by intraday and interday assays and the percentages of RSD were all within 10.6%. The recovery ranged from 60.2 to 77.9%. The method was successfully applied to pharmacokinetic study of all three aromatic acids and one monoterpene in rat plasma. Furthermore, we compared the pharmacokinetics profile of the four compounds in normal and primary dysmenorrhea rats' plasma following oral administration of Shaofu Zhuyu decoction (SFZYD) and its ethanol supernatant extract (SFE).
机译:我们开发了一种基于超高效液相色谱-串联质谱(UHPLC-MS / MS)的灵敏,快速的测定大鼠血浆中阿魏酸,咖啡酸,香草酸和pa药苷的方法。四种化合物的分离是在AcQuity UHPLC?上进行的。 BEH C18色谱柱,使用由乙腈和水(含0.1%甲酸)组成的流动相。正离子和负离子模式下的电喷雾电离以及多反应监测用于鉴定和定量活性成分。对于所有成分,所有浓度范围为4.24-2875 ngmL -1的校准曲线均具有良好的线性(r> 0.991)。通过日内和日间分析评估了体内研究的准确性,RSD的百分比均在10.6%以内。回收率从60.2%到77.9%。该方法已成功应用于大鼠血浆中所有三种芳香酸和一种单萜的药代动力学研究。此外,我们比较了口服少fu逐瘀汤(SFZYD)及其乙醇上清液提取物(SFE)后正常和原发性痛经大鼠血浆中这四种化合物的药代动力学。

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