首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Determination of honokiol and magnolol in cortex Magnoliae Officinalis by capillary electrophoresis with electrochemical detection.
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Determination of honokiol and magnolol in cortex Magnoliae Officinalis by capillary electrophoresis with electrochemical detection.

机译:毛细管电泳-电化学检测法测定厚朴中厚朴酚和厚朴酚的含量。

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摘要

Capillary electrophoresis with electrochemical detection has been employed for the determination of honokiol and magnolol in Cortex Magnoliae Officinalis (i.e. Magnolia Bark) for the first time. 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 microm diameter carbon disc electrode at a working potential of +0.90 V (versus saturated calomel electrode (SCE)). The two analytes can be well separated within 6 min in a 40 cm length fused silica capillary at a separation voltage of 18 kV in a 50mM borate buffer (pH 9.2). The relation between peak current and analyte concentration was linear over about three orders of magnitude with the detection limits (S/N=3) of 0.38 and 0.51 microM for honokiol and magnolol, respectively. The proposed method has been successfully applied to monitor the two bioactive constituents in the real plant samples with satisfactory assay results.
机译:带有电化学检测的毛细管电泳已首次用于测定厚朴中的厚朴酚和厚朴酚(即厚朴皮)。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。检测电极是工作电位为+0.90 V的直径为300微米的碳盘电极(相对于饱和甘汞电极(SCE))。在40m长的熔融石英毛细管中,在18mV的分离电压下,在50mM硼酸盐缓冲液(pH 9.2)中,可以在6分钟内将两种分析物很好地分离。峰值电流和分析物浓度之间的关系在大约三个数量级上呈线性关系,厚朴酚和厚朴酚的检出限(S / N = 3)分别为0.38和0.51 microM。所提出的方法已成功应用于监测真实植物样品中的两种生物活性成分,并获得令人满意的测定结果。

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