首页> 外文期刊>Medicinal chemistry research: an international journal for rapid communications on design and mechanisms of action of biologically active agents >Simultaneous determination of seven active ingredients in rat plasma by UPLC-MS/MS and application in pharmacokinetic studies after oral administration of scutellaria-coptis herb couple
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Simultaneous determination of seven active ingredients in rat plasma by UPLC-MS/MS and application in pharmacokinetic studies after oral administration of scutellaria-coptis herb couple

机译:用黄-药复方口服UPLC-MS / MS同时测定大鼠血浆中的7种活性成分并在药代动力学研究中应用

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摘要

A sensitive and rapid method for simultaneous determination of baicalin, baicalein, wogonoside, wogonin, berberine, copstisine and palmatine of Scutellaria baicalensis, and Coptidis rhizoma extract in rat plasma based on ultra high-performance liquid chromatography coupled with tandem mass spectrometry (UPLC-MS/MS) was developed. Plasma samples were processed by protein precipitation with methanol. Chromatographic analysis was performed on an Acquity BEH C18 column (100 mm x 2.1 mm, 1.7 A mu m) using a mobile phase consisting of acetonitrile and water (containing 0.1 % formic acid). Electrospray ionization in positive ion mode and multiple reaction monitoring were used to identify and quantify active components. All calibration curves gave good linearity (r > 0.991) over the concentration range from 0.72 to 375 ng/mL for all components. Recovery was 58.11-102.83 % depending on the analyte, and inter-day variability was less than 13 %. The lower limit of quantification for all compounds was between 0.82 and 1.33 ng/mL. The intra- and inter-day precision and accuracy of the quality control samples at three concentrations showed a parts per thousand currency sign14.7 % relative standard deviation and 86.6-105.5 % accuracy. The validated method was successfully applied to determine the concentrations of seven bioactive components in rat plasma after oral administration of Radix scutellariae and Coptidis rhizoma extract.
机译:基于高效液相色谱-串联质谱(UPLC-MS)的灵敏,快速的方法同时测定黄S中黄ical苷,黄e苷,wogonoside,wogonin,小ber碱,copstisine和棕榈黄素以及黄连提取物的含量/ MS)。血浆样品通过甲醇蛋白沉淀处理。在Acquity BEH C18色谱柱(100 mm x 2.1 mm,1.7 Aμm)上,使用由乙腈和水(含0.1%甲酸)组成的流动相进行色谱分析。正离子模式下的电喷雾电离和多反应监测用于鉴定和定量活性成分。所有组分的浓度范围为0.72至375 ng / mL,所有校准曲线均具有良好的线性(r> 0.991)。取决于分析物,回收率为58.11-102.83%,并且日间变化小于13%。所有化合物的定量下限在0.82和1.33 ng / mL之间。在三个浓度下,质量控制样品的日内和日间精度和准确度显示出千分之一货币符号相对标准偏差的14.7%和准确度的86.6-105.5%。经验证的方法已成功应用于口服黄和黄连提取物后测定大鼠血浆中七种生物活性成分的浓度。

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