文章摘要
高青山,袁 亮,王 彦,阎 超.超高效液相色谱法测定麻黄中l-麻黄碱和d-伪麻黄碱的含量[J].,2020,(5):832-837
超高效液相色谱法测定麻黄中l-麻黄碱和d-伪麻黄碱的含量
Determination of l-Ephedrine and d-Pseudoephedrine by Ultra Performance Liquid Chromatography
投稿时间:2019-07-28  修订日期:2019-08-23
DOI:10.13241/j.cnki.pmb.2020.05.007
中文关键词: 超高效液相色谱  l-麻黄碱  d-伪麻黄碱  非对映异构体  含量测定
英文关键词: Ultra high performance liquid chromatography (UPLC)  l-Ephedrine  d-Pseudoephedrine  Diastereomer  Content determination
基金项目:国家自然科学基金项目(21874088)
作者单位E-mail
高青山 1 上海交通大学药学院 上海 200240 2罗氏研发(中国)有限公司 上海 201203 qingshangao@163.com 
袁 亮 罗氏研发(中国)有限公司 上海 201203  
王 彦 上海交通大学药学院 上海 200240  
阎 超 上海交通大学药学院 上海 200240  
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中文摘要:
      摘要 目的:建立超高效液相色谱法(UPLC)测定麻黄中l-麻黄碱和d-伪麻黄碱含量的方法,为麻黄药材质量评价提供依据。方法:UPLC测定麻黄碱色谱柱为Waters Acquity BEH-C18 (2.1 mm × 50 mm, 1.7 μm);检测波长:214 nm;流动相为0.15%氨水水溶液(A)和乙腈( B ),梯度洗脱(0.0~4.0 min,5% B→55% B;4.0~ 4.1 min,55% B→95% B;4.1~4.7 min,95% B;4.7~4.8 min,95% B→5% B;4.8~5.0 min,5% B),流速:0.7 mL/min;柱温:25 ℃。结果:l-麻黄碱和d-伪麻黄碱分别在12.50~500.00 μg/mL和10.50~420.00 μg/mL范围内具有良好的线性关系,相关系数均为0.9999,UPLC方法测定l-麻黄碱和d-伪麻黄碱的回收率分别为101.99 %和98.68%。应用UPLC方法测定麻黄药材中的l-麻黄碱和d-伪麻黄碱的含量,麻黄药材两者含量分别为0.80%和0.18 %。结论:与常规HPLC测定l-麻黄碱和d-伪麻黄碱含量方法比较,本文所用方法测定结果更加准确、全面、且重复性好,能够快速测定麻黄药材中的l-麻黄碱和d-伪麻黄碱的实际含量;并且对麻黄碱及相关物质的测定有一定的指导意义。
英文摘要:
      ABSTRACT Objective: To establish a method based on ultra-high performance liquid chromatography (UPLC) for analysis of l-Ephedrine and d-Pseudoephedrine, providing the basis for their qualitative evaluation of Ephedra sinica. Methods: l-Ephedrine and d-Pseudoephedrine were separated on Waters Acquity BEH-C18 (2.1 mm × 50 mm, 1.7 μm). The detection wavelength was 214 nm. Mobile phase A was 0.15% ammonium in water and B was acetonitrile with gradient elution(0.0~4.0 min, 5% B→55% B; 4.0~4.1 min, 55% B→95% B; 4.1~4.7 min, 95% B; 4.7~4.8 min, 95% B→5% B; 4.8~5.0 min, 5% B). The flow rate was 0.7 mL/min. Column temperature was 25 ℃. Results: The developed method had good linearity in the range of 12.50~500.00 μg/mL for l-Ephedrine and 10.50~420.00 μg/mL for d-Pseudoephedrine respectively, and both of the correlation coefficients were 0.9999. The recoveries of UPLC method for l-Ephedrine and d-Pseudoephedrine were 101.99% and 98.68%, respectively. The content determination of l-Ephedrine and d-Pseudoephedrine from E. sinica was used by the UPLC method, the obtained results of l-Ephedrine and d-Pseudoephedrine were 0.80% and 0.18%, respectively. Conclusion: Compared with the commonly used content determination of l-Ephedrine and d-Pseudoephedrine by HPLC, the established method has been proven to be accurate, comprehensive and reproducible, and can be applied for rapid determination of l-Ephedrine and d-Pseudoephedrine for E. sinica. Furthermore, it might shed light on the determination of ephedrine and related substance.
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