首页 | 本学科首页   官方微博 | 高级检索  
检索        

麻黄标准汤剂质量评价体系的建立
引用本文:仝家羽,赵嵘,代云桃,范自全,王丹丹,秦雪梅,陈士林.麻黄标准汤剂质量评价体系的建立[J].中国中药杂志,2017,42(5):823-829.
作者姓名:仝家羽  赵嵘  代云桃  范自全  王丹丹  秦雪梅  陈士林
作者单位:中国中医科学院 中药研究所, 北京 100700;山西大学 中医药现代研究中心, 山西 太原 030006;山西大学 化学化工学院, 山西 太原 030006,中国中医科学院 中药研究所, 北京 100700,中国中医科学院 中药研究所, 北京 100700,沃特世科技(上海)有限公司, 上海 201206,沃特世科技(上海)有限公司, 上海 201206,山西大学 中医药现代研究中心, 山西 太原 030006,中国中医科学院 中药研究所, 北京 100700
基金项目:中国中医科学院综合性大平台项目(Z131100006513017-07)
摘    要:建立麻黄标准汤剂质量控制方法,为所有中药饮片标准汤剂质量评价方法的制定提供参考。制备麻黄标准汤剂,建立UPLC-UV指纹图谱并测定其麻黄碱和伪麻黄碱总含量;采用UPLC-QTOF/MS对主要色谱峰进行结构确认,明确汤剂中的主要化学成分;计算出膏率、指标成分转移率、pH,评价工艺的稳定性。结果麻黄汤剂中麻黄碱与伪麻黄碱的平均总浓度为(2.11±0.70)g·L~(-1);所有麻黄水煎液指纹图谱相似度均大于0.85;麻黄标准汤剂对照指纹图谱主要共有峰有10个,包括生物碱、有机酸类和黄酮;麻黄标准汤剂出膏率为(17±3.2)%、麻黄碱与伪麻黄碱的整体转移率为(32.4±8.1)%。该文建立了系统评价麻黄标准汤剂的质量评价方法,为所有源于麻黄水煎液的制剂的质量控制标准的制定提供参考。

关 键 词:麻黄  标准汤剂/标准煎液  指纹图谱  含量测定  出膏率  转移率
收稿时间:2016/10/17 0:00:00

Establish quality evaluation system for standard Ephedrae Herba decoction
TONG Jia-yu,CHAO Jung,DAI Yun-tao,FAN Zi-quan,WANG Dan-dan,QIN Xue-mei and CHEN Shi-lin.Establish quality evaluation system for standard Ephedrae Herba decoction[J].China Journal of Chinese Materia Medica,2017,42(5):823-829.
Authors:TONG Jia-yu  CHAO Jung  DAI Yun-tao  FAN Zi-quan  WANG Dan-dan  QIN Xue-mei and CHEN Shi-lin
Institution:Institute of Chinese Material Medica, China Academy of Chinese Medical Sciences, Beijng 100700, China;Shanxi University, Modern Research Center for Traditional Chinese Medicine, Taiyuan 030006, China;Shanxi University, College of Chemisrtry & Chemical Engineering, Taiyuan 030006, China,Institute of Chinese Material Medica, China Academy of Chinese Medical Sciences, Beijng 100700, China,Institute of Chinese Material Medica, China Academy of Chinese Medical Sciences, Beijng 100700, China,Waters Technologies(Shanghai) Limited, Shanghai 201206, China,Waters Technologies(Shanghai) Limited, Shanghai 201206, China,Shanxi University, Modern Research Center for Traditional Chinese Medicine, Taiyuan 030006, China and Institute of Chinese Material Medica, China Academy of Chinese Medical Sciences, Beijng 100700, China
Abstract:To establish the quality control methods for the standard decoction of Ephedrae Herba, and provide the reference for quality evaluation method of all Chinese herbal medicine decoction.Standard decoction of Ephedrae Herba was prepared, and UPLC-UV fingerprint was established to determine the total contents of ephedrine and pseudoephedrine. Then UPLC-QTOF/MS was used to confirm the major common peaks in the fingerprint to clarify the main chemical constituents in the decoction. In addition, the stability of the process was evaluated by calculating the parameters such as the extraction ratio, transfer rate of the index components and the pH values.In the decoction of Ephedrae Herba, the total average concentration of ephedrine and pseudoephedrine was (2.11±0.70) g·L-1; the similarities of all the fingerprints were more than 0.85; there were 10 major common peaks in the fingerprint, including alkaloids, flavonoids and organic acids; the extraction ratio was (17±3.2)%, and the overall transfer rate of ephedrine and pseudoephedrine was (32.4±8.1)%.The method for evaluating the quality of standard decoction of Ephedrae Herba was established in this article, providing reference for the quality control of products which were stemmed from the water extract of Ephedrae Herba.
Keywords:Ephedrae Herba  standard decoction  fingerprint  content determination  extraction ratio  transfer rate
本文献已被 CNKI 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号