...
首页> 外文期刊>Talanta: The International Journal of Pure and Applied Analytical Chemistry >Rapid analysis of pseudolaric acids in Cortex Pseudolaricis and related medicinal products by high performance liquid chromatography
【24h】

Rapid analysis of pseudolaric acids in Cortex Pseudolaricis and related medicinal products by high performance liquid chromatography

机译:高效液相色谱法快速分析伪皮层及相关药品中的伪laric acid

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

A simple,rapid,reverse-phase high performance liquid chromatographic method was developed for the quantitative analysis of pseudolaric acids in Cortex Pseudolaricis and its related medicinal products.With a C18 analytical column(4.6 mm x 150 mm i.d.),five pseudolaric acids,namely pseudolaric acids A-C,pseudolaric acid A-O-B-D-glucopyranoside and pseudolaric acid B-O-beta-D-glucopyranoside,were well separated within 7 min.Acetonitrile and 0.10% acetic acid were used as the mobile phase in a gradient program.The UV detection wavelength was set at 260 nm.The detection limits and quantification limits ranged in 8.26-16.66 ng/ml and 27.54-55.53 ng/ml,respectively.The intra-and inter-day variations were less than 1% for all five compounds.The recovery of all spiked pseudolaric acids ranged from 99.1% to 101.9%.Compared to existing analytical methods,this new method not only used two more important chemical markers but also provided a fivefold reduction in analysis time.In addition,the extraction method of herb sample was also modified by an orthogonal array experiment on three variable parameters:extraction time,solvent volume,and extraction cycles.The optimized extraction method was much simpler and could be efficiently used to analyse large set of herbal materials and related medicinal products.Nineteen herb samples collected from different regions of China and five related products were examined with this new analytical method.The results showed that this method is effective in distinguishing adulterants and unqualified products.
机译:建立了一种简便,快速,反相的高效液相色谱方法,用于定量分析伪皮层及其相关药品中的伪油酸。采用C18分析柱(4.6 mm x 150 mm内径),五种伪油酸在7分钟内将假laric酸AC,伪十二酸AOBD-吡喃葡萄糖苷和伪laric酸BO-β-D-吡喃葡萄糖苷很好地分离。在梯度程序中以乙腈和0.10%乙酸作为流动相。设置了UV检测波长在260 nm处,检测限和定量限分别为8.26-16.66 ng / ml和27.54-55.53 ng / ml。五种化合物的日内和日间变化均小于1%。加标的伪laric acid范围从99.1%到101.9%。与现有的分析方法相比,该新方法不仅使用了两个更重要的化学标记,而且分析时间缩短了五倍。还通过正交实验对提取时间,溶剂量和提取周期这三个变量参数进行了改进,优化了提取方法,简化了提取方法,可以有效地分析各种草药和相关药物。用这种新的分析方法对来自中国不同地区的19种草药样品和5种相关产品进行了检测,结果表明该方法可有效鉴别掺假品和不合格品。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号