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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Simultaneous determination of anthraquinones in radix Polygoni multiflori by capillary gas chromatography coupled with flame ionization and mass spectrometric detection
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Simultaneous determination of anthraquinones in radix Polygoni multiflori by capillary gas chromatography coupled with flame ionization and mass spectrometric detection

机译:毛细管气相色谱-火焰电离-质谱联用法同时测定何首乌中的蒽醌

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摘要

A rapid, accurate and reliable analytical method was developed for the simultaneous determination of five major anthraquinones, aloe-emodin, chrysophanol, emodin, physcion, and rhein, in radix Polygoni multiflori, a traditional Chinese herbal medicine. The method comprises a fast ultrasonic extraction with methanol and derivatization with N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA) + 1% trimethylchlorosilane (TMCS) followed by capillary gas chromatographic (GC) separation. The effect of reaction time on the derivatization of anthraquinones was examined. A baseline separation of the anthraquinone and internal standard derivatives was achieved in 15 min. The detection limits range from 0.22 to 0.60 mu g/mL for the five anthraquinones. The calibration curves are linear over the concentration range studied (from the detection limits to 40.0 mu g/mL) with the squares of correlation coefficients, R-2, greater than 0.998. The developed method was successfully applied to the simultaneous determination of anthraquinones in radix P. multiflori samples. The peak identification was confirmed using GC-MS. The contents of anthraquinones in radix P. multiflori samples studied were 27.41, 289.6, 64.22, 202.1, 288.6 mu g/g for chrysophanol, emodin, aloe-emodin, physcion, rhein, respectively. All relative standard deviations are less than 3.2%. The recoveries range from 80.2% to 119.3% for the five analytes. To the authors' best knowledge, this is the first GC method reported for the simultaneous determination of the five anthraquinones in radix P. multiflori. (c) 2008 Elsevier B.V. All rights reserved.
机译:建立了一种快速,准确,可靠的分析方法,可同时测定中草药何首乌中的五种主要蒽醌,芦荟大黄素,香豆酚,大黄素,physcion和大黄酸。该方法包括用甲醇快速超声提取并用N,O-双(三甲基甲硅烷基)三氟乙酰胺(BSTFA)+ 1%三甲基氯硅烷(TMCS)衍生化,然后进行毛细管气相色谱(GC)分离。考察了反应时间对蒽醌衍生化的影响。在15分钟内实现了蒽醌和内标衍生物的基线分离。五个蒽醌的检出限为0.22至0.60μg / mL。校正曲线在所研究的浓度范围内(从检测限到40.0μg / mL)是线性的,相关系数的平方R-2大于0.998。所开发的方法成功地用于同时测定何首乌样品中蒽醌的含量。使用GC-MS确认峰鉴定。对于多酚,大黄素,大黄素,芦荟大黄素,physcion和大黄酸,所研究的何首乌样品中蒽醌的含量分别为27.41、289.6、64.22、202.1、288.6μg / g。所有相对标准偏差均小于3.2%。五个分析物的回收率从80.2%到119.3%。据作者所知,这是首次报道的同时测定何首乌中五个蒽醌含量的气相色谱方法。 (c)2008 Elsevier B.V.保留所有权利。

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