首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Simultaneous determination of paeoniflorin from total glucosides of paeony in Sprague-Dawley rats and spontaneously hypertensive rats by high-performance liquid chromatography-tandem mass spectrometry: in vivo and in vitro studies
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Simultaneous determination of paeoniflorin from total glucosides of paeony in Sprague-Dawley rats and spontaneously hypertensive rats by high-performance liquid chromatography-tandem mass spectrometry: in vivo and in vitro studies

机译:通过高效液相色谱 - 串联质谱法同时测定Spraue-Dawley大鼠的芍药苷和自发性高血压大鼠中的芍药苷:体内和体外研究

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摘要

Paeoniflorin is a well-known monoterpene glucoside in the herbal drug that exhibits a number of biological activities. The pharmacokinetic characteristics of paeoniflorin from total glucosides of paeony in spontaneously hypertensive rats (SHR) are still unclear. It is essential to investigate the in vivo and in vitro pharmacokinetic differences of paeoniflorin from total glucosides of paeony in Sprague-Dawley (SD) and SHR. The in vivo pharmacokinetic data were analyzed using DAS 2.0 software and the in vitro metabolic characteristics were measured using rat hepatic microsomes. The concentration of paeoniflorin in biological samples was determined using high-performance liquid chromatography-electrospray ionization tandem mass spectrometry method, which showed good precision and stability. The plasma concentration-time profiles of paeoniflorin following oral administration of total glucosides of paeony showed a single peak and there were significant differences in the mean values of AUC((0-t)), AUC((0-)), CLz/F and T-max between SD and SHR (p<0.05). The metabolic rate of paeoniflorin from total glucosides of paeony was slower in SHR than in SD rats (p<0.05). The results might be useful in further applications of paeoniflorin and total glucosides of paeony. Copyright (c) 2016 John Wiley & Sons, Ltd.
机译:Paeoniflorin是在草药中的众所周知的单萜葡萄糖苷,其具有许多生物活性。从自发性高血压大鼠(SHR)中Paeony的总葡萄糖苷从芍药苷的药代动力学特征仍然尚不清楚。在Sprague-Dawley(SD)和ShR中,探讨Paeoniflorin的体内和体外药代动力学差异。使用DAS 2.0软件分析体内药代动力学数据,使用大鼠肝微粒体测量体外代谢特性。使用高效液相色谱 - 电喷雾电离串联质谱法测定生物样品中芍药蛋白的浓度,显示出良好的精度和稳定性。芍药蛋白在口服施氮后芍药蛋白酶的血浆浓度 - 时间谱表现出单峰,AUC((0-T)),AUC((0-)),CLZ / F的平均值存在显着差异SD和SHR之间的T-MAX(P <0.05)。来自芍药磷的芍药蛋白的代谢率比SD大鼠较慢(P <0.05)。结果对于芍药苷和芍药的总葡萄糖苷的进一步应用可能是有用的。版权所有(c)2016 John Wiley&Sons,Ltd。

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