首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination of calycosin-7-O-beta-D-glucoside, ononin, astragaloside IV, astragaloside I and ferulic acid in rat plasma after oral administration of Danggui Buxue Tang extract for their pharmacokinetic studies by liquid chromatography-
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Simultaneous determination of calycosin-7-O-beta-D-glucoside, ononin, astragaloside IV, astragaloside I and ferulic acid in rat plasma after oral administration of Danggui Buxue Tang extract for their pharmacokinetic studies by liquid chromatography-

机译:口服当归补血汤提取物用于大鼠药动学的液相色谱法同时测定大鼠血浆中的calycosin-7-O-β-D-葡萄糖苷,ononin,黄芪甲苷IV,黄芪甲苷I和阿魏酸

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摘要

A sensitive and reliable high-performance liquid chromatography-mass spectrometry (HPLC-MS) was developed and validated for simultaneous quantification of five main bioactive components, i.e., calycosin-7-O-beta-D-glucoside, ononin, astragaloside IV, astragaloside I and ferulic acid in rat plasma after oral administration of Danggui Buxue Tang (DBT) extract. Plasma samples were extracted with solid-phase extraction (SPE) separated on an Inertsil ZORBAX C-18 column and detected by MS with electrospray ionization (ESI) interface in negative selective ion monitoring (SIM) mode. Calibration curves offered linear ranges of two orders of magnitude with r(2) > 0.99. The method had the lower limit quantification of 0.55, 0.46, 1.07, 1.12 and 4.6 ng/mL for calycosin-7-O-beta-D-glucoside, ononin, astragaloside IV, astragaloside I and ferulic acid, respectively, with precision less than 10%. The RSD of intra- and inter-day variations ranged from 2.10% to 6.19% and 2.37% to 6.72%. This developed method was subsequently applied to pharmacokinetic studies of the five compounds in rats successfully. (c) 2008 Elsevier B.V. All rights reserved.
机译:开发了灵敏可靠的高效液相色谱-质谱(HPLC-MS)并通过验证可同时定量五个主要生物活性成分,即calycosin-7-O-β-D-葡萄糖苷,ononin,黄芪甲苷IV,黄芪甲苷口服当归补血汤(DBT)提取物后,我和大鼠血浆中的阿魏酸。血浆样品采用在Inertsil ZORBAX C-18色谱柱上分离的固相萃取(SPE)进行萃取,并在负选择离子监测(SIM)模式下通过带有电喷雾电离(ESI)接口的MS进行检测。校准曲线提供两个数量级的线性范围,其中r(2)> 0.99。该方法对calycosin-7-O-β-D-葡萄糖苷,ononin,黄芪甲苷IV,黄芪甲苷I和阿魏酸的下限定量分别为0.55、0.46、1.07、1.12和4.6 ng / mL,其精密度小于10%。日内和日间变化的相对标准偏差范围为2.10%至6.19%和2.37%至6.72%。这种发达的方法随后成功地应用于大鼠中五种化合物的药代动力学研究。 (c)2008 Elsevier B.V.保留所有权利。

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