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首页> 外文期刊>Bulletin of the Korean Chemical Society >Quantitative Determination of Marker Compounds and Pattern Recognition Analysis for Quality Control of Alismatis Rhizoma by HPLC
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Quantitative Determination of Marker Compounds and Pattern Recognition Analysis for Quality Control of Alismatis Rhizoma by HPLC

机译:HPLC法定量测定樟子菊中的标记化合物含量及模式识别分析。

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摘要

A quantitative method for determining levels of three bioactive compounds based on pattern recognition was developed and fully validated for the quality control of Alismatis Rhizoma (AR) by HPLC. Separation conditions were optimised using an Optimapak C18 column (250 mm × 4.6 mm, 5 μm) with a mobile phase of acetonitrile and 0.1% aqueous phosphoric acid and detection wavelengths of 205 and 245 nm. Method validation yielded acceptable linearity (r2 0.9998) and percent recovery (98.06%-101.71%). Limits of detection ranged from 0.08 to 0.15 μg/mL. Levels of the three bioactive compounds, alisol C acetate, alisol B, and alisol B acetate, in AR were 0.07-0.45, 0.38-10.32, and 1.13-8.59 mg/g dried weight, respectively. Pattern analyses based on these three compounds were able to differentiate Chinese and Korean samples accurately. The results demonstrate that alisol B and its acetate may be used as marker compounds for AR quality and can be regulated to no less than 0.36 and 1.29 mg/g of dried sample, respectively. The method described here is suitable for quantitative analyses and quality control of multiple components in AR.
机译:建立了一种基于模式识别的测定三种生物活性化合物含量的定量方法,并通过HPLC对其进行了质量控制,充分验证了该方法的质量。使用Optimapak C18色谱柱(250 mm×4.6 mm,5μm)优化分离条件,该色谱柱的流动相为乙腈和0.1%磷酸水溶液,检测波长为205和245 nm。方法验证产生了可接受的线性(r2> 0.9998)和回收率(98.06%-101.71%)。检测限范围为0.08至0.15μg/ mL。在AR中,三种生物活性化合物的水平分别为0.07-0.45、0.38-10.32和1.13-8.59 mg / g干重。基于这三种化合物的模式分析能够准确地区分中国和韩国样品。结果表明,alisol B及其乙酸盐可用作AR品质的标记化合物,并可分别控制在干燥样品中不低于0.36和1.29 mg / g。此处描述的方法适用于AR中多个组件的定量分析和质量控制。

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