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High performance liquid chromatographic assay of saikosaponins from radix Bupleuri in China.

机译:高效液相色谱法测定中国柴胡中总皂苷的含量。

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In this study, the quantitative analysis of saikosaponins from Radix Bupleuri in China was performed by high performance liquid chromatography. Saikosaponin-a and -d were converted completely into saikosaponin-b1 and -b2 by mild acid treatment. Distinctive measuring of these converted diene-saponins provided a rapid and selective method for the determination of saikosaponin-a and -d in commercial samples of Radix Bupleuri. The conditions of extraction and conversion of saikosaponins were optimized using orthogonal design L9(3(4)). The HPLC analysis was performed on ODS-C18 column with a flow rate of 1.0 ml/min and detection wavelength of 250 nm. Well resolved chromatograms of saikosaponin-b1 and -b2 were obtained with an isocratic elution of acetonitrile : 1% formic acid water (37.5 : 62.5). Calibration curves of saikosaponin-b1 and -b2 were linear in the range of 4.9-98.0 microg/ml and 3.5-71.0 microg/ml, respectively. The average recovery of saikosaponin-b1 and -b2 were 98.3% (RSD = 3.1%) and 96.4% (RSD = 1.8%), respectively. Seventeen samples of different species and habitats of Radix Bupleuri were analyzed by the developed HPLC method.
机译:本研究采用高效液相色谱法对中国柴胡中的皂苷进行了定量分析。通过温和的酸处理,将皂苷-a和-d完全转化为皂苷-b1和-b2。这些转化的二烯-皂苷的独特测量提供了一种快速,选择性的方法,用于测定柴胡商业样品中的皂苷-a和-d。使用正交设计L9(3(4))优化了皂苷的提取和转化条件。 HPLC分析在ODS-C18柱上以1.0ml / min的流速和250nm的检测波长进行。在乙腈:1%甲酸水(37.5:62.5)的等度洗脱下,获得了Saikosaponin-b1和-b2的色谱图。 saikosaponin-b1和-b2的校准曲线分别在4.9-98.0 microg / ml和3.5-71.0 microg / ml范围内呈线性。 saikosaponin-b1和-b2的平均回收率分别为98.3%(RSD = 3.1%)和96.4%(RSD = 1.8%)。通过开发的HPLC方法分析了柴胡不同物种和生境的17个样品。

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