首页> 外文期刊>Journal of separation science. >Development and validation of a UHPLC-MS/MS method for the simultaneous determination of five bioactive flavonoids in rat plasma and comparative pharmacokinetic study after oral administration of Xiaochaihu Tang and three compatibilities
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Development and validation of a UHPLC-MS/MS method for the simultaneous determination of five bioactive flavonoids in rat plasma and comparative pharmacokinetic study after oral administration of Xiaochaihu Tang and three compatibilities

机译:UHPLC-MS / MS法同时测定大鼠血浆和比较药代动力学研究的UHPLC-MS / MS方法的开发和验证,少晶堂口服给药及三种兼容性

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摘要

An accurate, rapid, and reliable ultra high performance liquid chromatography with tandem mass spectrometry method was developed and validated for the simultaneous determination of baicalin, wogonoside, baicalein, wogonin, and oroxylin A in rat plasma. Then, the stability of baicalin and baicalein in the preparation of plasma sample was systematically investigated. The Waters BEH C-18 column was used with a gradient mobile phase system of acetonitrile and water containing 0.1% formic acid. The analytes were detected in the multiple reaction monitoring mode with positive electrospray ionization. 100 mu L fresh plasma was added with 50 mu L antioxidant reagent (1 mol/L HCl containing 0.5% Vitamin C), and liquid-liquid extraction with ethyl acetate was used to extract the analytes from plasma. Lower limits of quantification of baicalin, wogonoside, baicalein, wogonin, and oroxylin A were 21.9, 4.80, 1.20, 0.848, and 0.800 ng/mL, respectively. The mean extract recoveries of five flavonoids were 69.1 similar to 89.2%, and the precision and accuracy were within the acceptable limits. This method was further successfully applied to the comparative pharmacokinetic study of these five flavonoids in rats after oral administration of Xiaochaihutang and three compatibilities. The obtained results may be helpful to reveal the mechanism of Xiaochaihutang formula compatibility.
机译:开发并验证了具有串联质谱法的精确,快速和可靠的超高效液相色谱法,用于同时测定大鼠等离子体中的黄芩苷,Wogonoside,Baicalin,Wogonin和oroxylina。然后,系统地研究了在制备等离子体样品中的黄芩苷和Baicalin的稳定性。 Waters BH C-18柱与乙腈和含有0.1%甲酸的水的梯度流动相系统一起使用。在具有正电喷雾电离的多反应监测模式中检测分析物。加入100μl新鲜等离子体加入50μl抗氧化剂试剂(含有0.5%维生素C的1mol / L HCl),用乙酸乙酯的液 - 液提取从血浆中提取分析物。较低的量化黄芩苷,Wogonoside,BaciCalind,Wogonin和Oroxylin A的限制分别为21.9,4.80,1.20,0.848和0.800ng / ml。五种黄酮类化合物的平均提取物回收率为69.1,类似于89.2%,精度和精度在可接受的限度范围内。该方法进一步成功地应用于小昌塘和三种兼容性后大鼠该五种类黄酮的对比药代动力学研究。获得的结果可能有助于揭示小昌塘配方相容性的机制。

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