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首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Development of rapid and simultaneous quantitative method for green tea catechins on the bioanalytical study using UPLC/ESI-MS
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Development of rapid and simultaneous quantitative method for green tea catechins on the bioanalytical study using UPLC/ESI-MS

机译:利用UPLC / ESI-MS进行生物分析研究的快速同步定量绿茶儿茶素的方法开发

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摘要

A rapid and quantitative analytical method for the simultaneous determination of green tea catechins using ultra-performance liquid chromatography/electrospray ionization-mass spectrometry was developed. Total analytical run time was 3.5min for the detection of (-)-epicatechin (EC), (-)-epicatechin-3-O-gallate (ECG), (-)-epigallocatechin (EGC), (-)-epigallocatechin-3-O-gallate (EGCG) and myricetin as the internal standard (IS) in rat plasma. The calibration curves were linear over the range of 10-5000ng/mL for all the catechins. The inter- and intra-day precision (relative standard deviation) and accuracy (percentage deviation) of the method were both lower than 10%. The average extraction recoveries in plasma ranged from 68.5 to 86.5%, and the lower limits of quantification of EC, EGC, ECG and EGCG were 10ng/mL with a signal-to-noise ratio of >10. The assay developed was successfully applied to a pharmacokinetic study of catechins following intravenous and intragastric administrations of green tea extract in rats. Plasma concentrations of four catechins were detected up to 5-24h after administration, and the pharmacokinetic parameters of catechins were in agreement with previous studies. From these findings, taken together with the high productivity and precision, the developed method could be a reliable and reproducible tool for the evaluation of pharmacokinetic properties of catechins.
机译:建立了一种超高效液相色谱/电喷雾电离质谱法同时测定绿茶儿茶素的快速定量分析方法。检测(-)-表儿茶素(EC),(-)-表儿茶素-3-O-没食子酸酯(ECG),(-)-表没食子儿茶素(EGC),(-)-表没食子儿茶素-的总分析运行时间为3.5分钟大鼠血浆中的3-O-没食子酸酯(EGCG)和杨梅素作为内标(IS)。所有儿茶素的校准曲线在10-5000ng / mL范围内是线性的。该方法的日间和日内精度(相对标准偏差)和精度(百分比偏差)均低于10%。血浆中的平均提取回收率在68.5%至86.5%之间,EC,EGC,ECG和EGCG的定量下限为10ng / mL,信噪比> 10。在大鼠静脉内和胃内给予绿茶提取物后,开发的测定方法已成功地应用于儿茶素的药代动力学研究。给药后至5-24h时检测到四种儿茶素的血浆浓度,儿茶素的药代动力学参数与以前的研究一致。从这些发现中,结合高生产率和高精度,所开发的方法可能是评估儿茶素药代动力学特性的可靠且可重复的工具。

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