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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 of phenolic acids by UPLC-MS/MS in rat plasma and its application in pharmacokinetic study after oral administration of Flos Lonicerae preparations
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Simultaneous determination of phenolic acids by UPLC-MS/MS in rat plasma and its application in pharmacokinetic study after oral administration of Flos Lonicerae preparations

机译:口服金银花制剂中UPLC-MS / MS同时测定大鼠血浆中酚酸的含量及其在药代动力学研究中的应用

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摘要

The current study aims to investigate the pharmacokinetic study of five phenolic acids (neochlorogenic acid, chlorogenic acid, cryptochlorogenic acid, 3,5-dicaffeoylquinic acid and 3,4-dicaffeoylquinic acid) following oral administration of Flos Lonicerae preparations in rats. A rapid and sensitive ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed to simultaneously determine the five phenolic acids in rat plasma. After mixing with the internal standard (IS) tinidazole, plasma samples were pretreated by liquid-liquid extraction with ethyl acetate-hexane (9:1, v/v). The separation was performed on an Acquity UPLC BEH C18 column (100mm×2.1mm, 1.7μm) at a flow rate of 0.4mlmin-1, and acetonitrile/methanol (4:1, v/v)-0.4% formic acid was used as mobile phase. The detection was performed on a triple quadrupole tandem mass spectrometer by multiple reaction monitoring (MRM) via electrospray ionization (ESI) source with positive ionization mode. All calibration curves had good linearity (r0.991) over the concentration ranges of 0.74-378ngml-1 for neochlorogenic acid, 0.50-1030ngml-1 for chlorogenic acid, 1.9-250ngml-1 for cryptochlorogenic acid, 0.74-380ngml-1 for 3,5-dicaffeoylquinic acid, and 5.1-328ngml-1 for 3,4-dicaffeoylquinic acid. The intra-and inter-day precision were within 15% and the accuracy ranged from 86.2% to 114.1%.
机译:本研究旨在研究在大鼠中口服金银花制剂后五种酚酸(新绿原酸,绿原酸,隐绿原酸,3,5-二咖啡酰奎尼酸和3,4-二咖啡酰奎尼酸)的药代动力学研究。建立了一种快速灵敏的超高效液相色谱-串联质谱(UPLC-MS / MS)方法,可同时测定大鼠血浆中的五种酚酸。与内标(IS)替硝唑混合后,血浆样品通过乙酸乙酯/正己烷(9:1,v / v)液-液萃取进行预处理。在Acquity UPLC BEH C18色谱柱(100mm×2.1mm,1.7μm)上以0.4mlmin-1的流速进行分离,使用乙腈/甲醇(4:1,v / v)-0.4%甲酸作为流动相。通过多反应监测(MRM)通过正电离模式下的电喷雾电离(ESI)源在三重四极杆串联质谱仪上进行检测。所有校准曲线在新绿原酸0.74-378ngml-1,绿原酸0.50-1030ngml-1,隐绿原酸1.9-250ngml-1、0.74-380ngml-1 3的浓度范围内均具有良好的线性(r> 0.991) ,5-二咖啡酰基奎宁酸和5.1-328ngml-1用于3,4-二咖啡酰基奎宁酸。日内和日间精度在15%以内,精度范围为86.2%至114.1%。

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