首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Determination of flavonoids in Houttuynia cordata Thunb.and Saururus chinensis (Lour.)Bail.by capillary electrophoresis with electrochemical detection
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Determination of flavonoids in Houttuynia cordata Thunb.and Saururus chinensis (Lour.)Bail.by capillary electrophoresis with electrochemical detection

机译:毛细管电泳-电化学检测法测定鱼腥草和uru鱼中的黄酮类化合物。

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摘要

Four flavonoids (rutin, hyperoside, quercitrin and quercetin)in Houttuynia cordata Thunb.and Saururus chinensis (Lour.)Bail, were determined by capillary electrophoresis with wall-jet amperometric detection.The working electrode was a 500 mum diameter carbon disc electrode and the detection potential was +0.95 V (versus Ag/AgCl).Effects of several important factors, such as the running buffer and its corresponding pH and concentration, separation voltage, injection time were investigated to acquire the optimum conditions for separation of these four flavonoids.Baseline separation for the four flavonoids was obtained within 21 min in a 60 cm length capillary at a separation voltage of 15 kV with a 60mmoL/L Na_2B_4O_7-120mmoL/L NaH_2PO_4 buffer (pH 8.8)as running buffer.The relationship between peak currents and analyte concentrations was linear over about two orders of magnitude with detection limits (defined as S/N = 3)ranging from 0.02 to 0.05 mug/mL for all analytes.This method was applied for the determination of the above four flavonoids in H.cordata Thunb.and S.chinensis (Lour.)Bail, with simple extraction procedures, and the assay results were satisfactory.
机译:采用毛细管电泳-壁流-安培检测法测定鱼腥草和中山金银花中的四种类黄酮(芦丁,高甙,槲皮素和槲皮素),工作电极为直径500μm的碳圆盘电极。检测电位为+0.95 V(相对于Ag / AgCl)。研究了几个重要因素的影响,例如运行缓冲液及其相应的pH和浓度,分离电压,进样时间,以获取分离这四种类黄酮的最佳条件。使用60mmoL / L Na_2B_4O_7-120mmoL / L NaH_2PO_4缓冲液(pH 8.8)作为运行缓冲液,在15 kV分离电压下,在60厘米长的毛细管中于21分钟内获得了四种类黄酮的基线分离。分析物浓度在大约两个数量级上呈线性,所有分析物的检出限(定义为S / N = 3)为0.02至0.05杯/毫升。用该方法可简单地进行提取,同时测定金丝桃和中药材中的上述四种类黄酮,测定结果令人满意。

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