首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Simultaneous determination and pharmacokinetic study of stachydrine and leonurine in rat plasma after oral administration of Herba Leonuri extract by LC-MS/MS
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Simultaneous determination and pharmacokinetic study of stachydrine and leonurine in rat plasma after oral administration of Herba Leonuri extract by LC-MS/MS

机译:LC-MS / MS同时测定益母草提取物口服后大鼠血浆中水苏碱和利尿平的含量及药代动力学研究

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A simple, sensitive and specific method was developed for simultaneous determination of stachydrine and leonurine in rat plasma using diphenhydramine as an internal standard (IS). The separation was performed on an Agilent ZORBAX Eclipse XDB-C18 column (150mm??4.6mm, i.d., 5??m) at a flow rate of 0.6mL/min, and the mixture of methanol-water containing 0.1% formic acid was used as the mobile phase. The lower limits of quantitation (LLOQs) in rat plasma were 0.895 and 0.287ng/mL for stachydrine and leonurine, respectively. Intra- and inter-day precisions were within 14.4% and accuracies were not more than 3.0%. After single oral administration of 14.5g/kg Herba Leonuri extract, Cmax of stachydrine and leonurine in rat plasma were respectively 1608??267 and 43.3??8.2ng/mL, while Tmax values were respectively 0.75??0.27 and 0.83??0.26h. The results demonstrated that the present LC-MS/MS method was sensitive enough for pharmacokinetic study of stachydrine and leonurine following oral administration of Herba Leonuri extract. ? 2013 Elsevier B.V.
机译:建立了一种简单,灵敏,特异的方法,以苯海拉明为内标(IS)同时测定大鼠血浆中的水苏碱和利尿平。分离是在Agilent ZORBAX Eclipse XDB-C18色谱柱(150mm×4.6mm,内径,5μm)上以0.6mL / min的流速进行的,甲醇和水的混合物含0.1%的甲酸为用作流动相。水苏碱和利尿尿酸的血浆定量下限(LLOQs)分别为0.895和0.287ng / mL。日内和日间精度在14.4%以内,准确度不超过3.0%。单次口服14.5g / kg益母草提取物后,大鼠血浆中水苏碱和莱诺宁的Cmax分别为1608 ?? 267和43.3 ?? 8.2ng / mL,Tmax分别为0.75 ?? 0.27和0.83 ?? 0.26。 H。结果表明,目前的LC-MS / MS方法对于口服莱昂努里提取物后的水苏碱和利尿尿酸的药代动力学研究足够灵敏。 ? 2013年Elsevier B.V.

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