首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Fast Analysis of Puerarin and Daidzein in Radix puerariae and It's Medicinal Preparation by Micellar Electrokinetic Capillary Chromatography
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Fast Analysis of Puerarin and Daidzein in Radix puerariae and It's Medicinal Preparation by Micellar Electrokinetic Capillary Chromatography

机译:胶束电动毛细管色谱法快速分析葛根中的葛根素和大豆苷元及其药物制备

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摘要

A method was developed to determine puerarin and daidzein in Radix puerariae and it's medicinal preparation Gegen qinlianpian by micellar eletrokinetic capillary chromatography. The analytical conditions were optimized by investigating the effects of buffer pH and concentration, sodium dodecyl sulfate concentration and β-cyclodextrin. Under the optimized conditions, the two analytes were well separated in 5 min. A good linear relationship between the peak height and concentration was found in the 0.02-1.20 and 0.02-1.00 mg mL~(-1) concentration range for puerarin and daidzein, respectively. The relative standard deviation based on migration time and peak height were 0.51 and 1.82 % for puerarin, 0.45 and 1.68 % for daidzein, respectively. The detection limits were 0.005 and 0.004 mg mL~(-1) for puerarin and daidzein, respectively.
机译:建立了一种以胶束电动毛细管色谱法测定葛根及其药用制剂葛根ll连片中葛根素和大豆苷元的方法。通过研究缓冲液pH和浓度,十二烷基硫酸钠浓度和β-环糊精的影响来优化分析条件。在优化的条件下,两种分析物在5分钟内可以很好地分离。葛根素和大豆苷元的峰高与浓度在0.02-1.20和0.02-1.00 mg mL〜(-1)浓度范围内具有良好的线性关系。葛根素基于迁移时间和峰高的相对标准偏差分别为0.51和1.82%,黄豆苷元为0.45和1.68%。葛根素和大豆苷元的检出限分别为0.005和0.004 mg mL〜(-1)。

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