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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Simultaneous determination determination of ten bioactive constituents of Sanjie Zhentong Capsule in rat plasma by ultra-high-performance liquid chromatography tandem mass spectrometry and its application to a pharmacokinetic study
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Simultaneous determination determination of ten bioactive constituents of Sanjie Zhentong Capsule in rat plasma by ultra-high-performance liquid chromatography tandem mass spectrometry and its application to a pharmacokinetic study

机译:用超高效液相色谱串联质谱法同时测定三杰震孔胶囊中的10种生物活性成分胶囊中的大鼠血浆中的生物活性成分及其在药代动力学研究中的应用

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摘要

Sanjie Zhentong capsule, a well-known traditional Chinese medicine prescription, are used for the treatment of endometriosis-related diseases. In this study, a simple, rapid and sensitive ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method was developed for the simultaneous determination of ten bioactive constituents, including peimine, peiminine, peimisine, loureirin A, loureirin B, 7,4'-dihydroxyflavone, pterostilbene, ginsenoside Rgl, ginsenoside Rb1, and notoginsenoside R1 in rat plasma after oral administration of Sanjie Zhentong capsule. The sample preparations for protein removal was accomplished using a simple methanol precipitation method. The analytes were completely separated from the endogenous compounds on an Agilent Poroshell 120 SB-C18 column (4.6 mm x 150 mm, 2.7 mu m) using an isocratic elution with methanol - 0.1% formic acid aqueous (4/1, v/v) as a mobile phase. The single-run analysis time was as short as 14.0 min. The inter-day and intra-day precision of the quality control samples exhibited relative standard deviations (RSD) <9.5% and the accuracy values ranged from -8.6% to 15.0%. The lower limits of quantification (LLOQ) were 10, 10, 10, 10, 10, 10, 5, 10, 10 and 20 ng/mL for peimine, peiminine, peimisine, loureirin A, loureirin B, 7,4'-dihydroxyflavone, pterostilbene, ginsenoside Rgl, ginsenoside Rb1, notoginsenoside RI, respectively. The analytical method was successfully applied to a pharmacokinetic study of the multi-components after oral administration of Sanjie Zhentong Capsule in rats. (C) 2017 Published by Elsevier B.V.
机译:散结止痛胶囊是一种著名的中药处方,用于治疗子宫内膜异位症相关疾病。本研究建立了一种简便、快速、灵敏的超高效液相色谱-串联质谱(UHPLC-MS/MS)方法,用于同时测定十种生物活性成分,包括贝母碱、贝母碱、贝母碱、罗勒素a、罗勒素B、7,4'-二羟基黄酮、紫檀烯、人参皂苷Rgl、人参皂苷Rb1、,口服三节镇痛胶囊后大鼠血浆中三七皂苷R1的含量。使用简单的甲醇沉淀法完成蛋白质去除的样品制备。在安捷伦Poroshell 120 SB-C18柱(4.6 mm x 150 mm,2.7μm)上,使用甲醇-0.1%甲酸水溶液(4/1,v/v)作为流动相的等度洗脱,将分析物与内源性化合物完全分离。单次分析时间短至14.0分钟。质控样品的日间和日间精密度显示相对标准偏差(RSD)<9.5%,准确度值范围为-8.6%至15.0%。培亚胺、培亚胺、培亚胺、罗瑞林A、罗瑞林B、7,4'-二羟基黄酮、紫檀烯、人参皂甙Rgl、人参皂甙Rb1、三七皂甙RI的定量下限(LLOQ)分别为10、10、10、10、10、5、10、10和20 ng/mL。该分析方法已成功应用于大鼠口服三节镇痛胶囊后多组分的药代动力学研究。(C) 2017年由爱思唯尔B.V.出版。

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