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UHPLC-MS 同时测定大鼠口服芍药甘草汤后血浆中三种芳香酸和一种单萜的含量及药代动力学研究。

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

机构信息

Jiangsu Key Laboratory for TCM Formulae Research, Nanjing University of Chinese Medicine, Nanjing 210046, P. R. China.

出版信息

Am J Chin Med. 2013;41(3):697-715. doi: 10.1142/S0192415X13500481.

Abstract

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).

摘要

我们建立了一种灵敏、快速的超高效液相色谱-串联质谱法(UHPLC-MS/MS)测定大鼠血浆中阿魏酸、咖啡酸、香草酸和芍药苷的方法。四种化合物在 AcQuity UHPLC™ BEH C18 柱上,以乙腈和水(含 0.1%甲酸)为流动相进行分离。采用电喷雾离子化正、负离子模式和多反应监测对活性成分进行鉴定和定量。所有校准曲线的浓度范围为 4.24-2875 ngmL(-1),均具有良好的线性(r > 0.991)。体内研究的精密度通过日内和日间测定进行评估,RSD 的百分比均在 10.6%以内。回收率在 60.2%至 77.9%之间。该方法成功应用于大鼠血浆中三种芳香酸和一种单萜类化合物的药代动力学研究。此外,我们比较了口服芍药甘草汤(SFZYD)及其醇上清液提取物(SFE)后正常和原发性痛经大鼠血浆中四种化合物的药代动力学特征。

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