首页> 外文期刊>Analytical and Bioanalytical Chemistry >Simultaneous determination of p-hydroxyacetophenone, chlorogenic acid, and caffeic acid in Herba Artemisiae Scopariae by capillary electrophoresis with electrochemical detection
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Simultaneous determination of p-hydroxyacetophenone, chlorogenic acid, and caffeic acid in Herba Artemisiae Scopariae by capillary electrophoresis with electrochemical detection

机译:毛细管电泳-电化学检测法同时测定青蒿中对羟基苯乙酮,绿原酸和咖啡酸

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摘要

Capillary electrophoresis with electrochemical detection has been employed for the determination of p-hydroxyacetophenone, chlorogenic acid, and caffeic acid in Herba Artemisiae Scopariae (the dried sprout of Artemisia scoparia Waldst. et Kit.). The effects of several important factors, such as the concentration and the acidity of the running buffer, separation voltage, injection time, and detection potential, were investigated to acquire the optimum conditions. The detection electrode was a 300-μm-diameter carbon disc electrode at a working potential of +0.90 V (relative to the saturated calomel electrode). The three analytes can be well separated within 11 min in a 40-cm-long fused-silica capillary at a separation voltage of 15 kV in 50 mM borate buffer (pH 9.2). The relation between peak current and analyte concentration was linear over about 3 orders of magnitude, with detection limits (signal-to-noise ratio of 3) of 0.31, 0.39, and 0.50 μM for p-hydroxyacetophenone, chlorogenic acid, and caffeic acid, respectively. The proposed method has been successfully applied to monitor the three bioactive constituents in real plant samples and to differentiate between different herbal drugs with satisfactory assay results.
机译:带有电化学检测功能的毛细管电泳已用于测定中草药蒿(干蒿的干芽)中对羟基苯乙酮,绿原酸和咖啡酸的含量。研究了几个重要因素的影响,例如运行缓冲液的浓度和酸度,分离电压,进样时间和检测电位,以获取最佳条件。检测电极是直径为300μm的碳盘电极,工作电位为+0.90 V(相对于饱和甘汞电极)。在50 mM硼酸盐缓冲液(pH 9.2)中,在15 kV的分离电压下,可以在40 cm长的熔融石英毛细管中在11分钟内将三种分析物很好地分离。峰值电流与分析物浓度之间的关系在大约3个数量级上呈线性关系,对羟基苯乙酮,绿原酸和咖啡酸的检出限(信噪比为3)为0.31、0.39和0.50μM,分别。所提出的方法已成功应用于监测真实植物样品中的三种生物活性成分,并以令人满意的测定结果区分不同草药。

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