...
首页> 外文期刊>Journal of liquid chromatography and related technologies >A Rapid Hydrophilic Interaction Liquid Chromatographic Method for Simultaneous Determination of Three Ephedrine Alkaloids in Ephedra Herb and Its Preparations
【24h】

A Rapid Hydrophilic Interaction Liquid Chromatographic Method for Simultaneous Determination of Three Ephedrine Alkaloids in Ephedra Herb and Its Preparations

机译:快速亲水相互作用色谱法同时测定麻黄中三种麻黄碱及其制备方法

获取原文
获取原文并翻译 | 示例
           

摘要

A rapid hydrophilic interaction liquid chromatographic method has been developed and validated for simultaneous quantitative analysis of methylephedrine, ephedrine, and pseudoephedrine in Ephedra Herb and its preparations. The chromatographic method was performed using a mobile phase consisted of acetonitrile-ammonium acetate (pH 5.0; 0.195M) (95:5, v/v), running at 1.5mL min(-1) on a Pinnacle II Cyano column (5 mu m, 150x4.6mm) at 30 degrees C. The detector wavelength was set at 208nm. The chromatographic method was validated for specificity, linearity and range, limit of detection and quantification, precision, stability, repeatability, and accuracy. The main parameters were specificity (peak purity match factors were >980), linearity (r>0.9996), intra- and inter-day precisions (RSD %, 0.48 similar to 1.70, and RSD %, 0.81 similar to 1.86, respectively), limit of detections and quantifications (29.49 and 98.31ngmL(-1) for methylephedrine; 47.74 and 159.1ngmL(-1) for ephedrine; 121.8 and 406.0ngmL(-1) for pseudoephedrine). The standard addition recoveries were in the range of 86.84 similar to 102.1% and the RSDs of them were <5.23% in samples. The main mechanism was discussed from properties of analytes and optimized process. The results indicated the developed method was rapid (8min), sensitive, and accurate for simultaneous determination of the analytes in Ephedra Herb and its three preparations.
机译:已开发出一种快速亲水相互作用液相色谱方法,并已验证了该方法可同时定量分析麻黄及其制剂中的甲基麻黄碱,麻黄碱和伪麻黄碱。使用由乙腈-乙酸铵(pH 5.0; 0.195M)(95:5,v / v)组成的流动相进行色谱法,在Pinnacle II Cyano色谱柱(5 mu m,150x4.6mm)在30摄氏度。检测器波长设置为208nm。对色谱方法的特异性,线性和范围,检测和定量限,精度,稳定性,可重复性和准确性进行了验证。主要参数是特异性(峰纯度匹配因子> 980),线性(r> 0.9996),日内和日间精度(RSD%,0.48类似于1.70,RSD%,0.81类似于1.86),检测和定量限(甲基麻黄碱为29.49和98.31ngmL(-1);麻黄碱为47.74和159.1ngmL(-1);伪麻黄碱为121.8和406.0ngmL(-1))。标准加样回收率在86.84的范围内,与102.1%相似,并且样品的RSD小于<5.23%。从分析物的性质和优化工艺上讨论了其主要机理。结果表明,所开发的方法快速(8分钟),灵敏且准确,可同时测定麻黄及其三种制剂中的分析物。

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