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HPLC法同时测定升麻葛根汤中3个有效成分的含量
姚少姿1,2, 常梦春1,2, 卢鹏1,2, 王金艳1,2, 陈世彬3, 刘静静1,2, 刘志东1,2
1.天津中医药大学, 现代中药发现与制剂技术教育部工程研究中心, 天津 300193;2.天津中医药大学, 天津市现代中药重点实验室-省部共建国家重点实验室培育基地, 天津 300193;3.华润三九医药股份有限公司, 深圳 518110
摘要:
[目的]用高效液相色谱(HPLC)法,建立一种能同时测定升麻葛根汤汤剂中异阿魏酸、葛根素和芍药苷含量的分析方法。[方法]Waters XBridge® Shield RP18色谱柱(250 mm×4.6 mm,5 μm),流动相:甲醇-0.05 mol/L磷酸二氢钾为流动相,梯度洗脱,体积流量为0.8 mL/min,双波长检测,检测波长分别为230 nm、317nm,柱温30℃。[结果]芍药苷、葛根素和异阿魏酸在该色谱条件下能分离良好,且阴性无干扰。其中芍药苷、葛根素和异阿魏酸的线性范围分别为0.382~6.118 μg、1.602~25.626 μg和0.081~1.303 μg;平均回收率(n=6)分别为101.5%、102.9%和98.1%,RSD均小于3.0%。[结论]本方法操作简便、准确、重复性好,可同时测定升麻葛根汤中芍药苷、葛根素和异阿魏酸的含量,为升麻葛根汤的质量评价提供科学依据。
关键词:  升麻葛根汤  高效液相色谱法  异阿魏酸  葛根素  芍药苷
DOI:10.11656/j.issn.1672-1519.2017.05.18
分类号:
基金项目:“十二五”重大新药创制项目(2013ZX09508-105)。
Simultaneous determination of three active components in decoction of rhizoma cimicifugae and radix puerariae by HPLC
YAO Shao-zi1,2, CHANG Meng-chun1,2, LU Peng1,2, WANG Jin-yan1,2, CHEN Shi-bin3, LIU Jing-jing1,2, LIU Zhi-dong1,2
1.Engineering Research Center of Modern Chinese Medicine Discovery and Preparation Technique, Ministry of Education, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China;2.Tianjin State Key Laboratory of Modern Chinese Medicine-Province and Mimstry Co-established state Key Laboratory Cultivation Base, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China;3.China Resources of Sanjiu Medical & Pharmaceutical Co. Ltd. Shenzhen 518110, China
Abstract:
[Objective] To develop an analytical method for simultaneously determining the contents of paeoniflorin, puerarin and isoferulic acid in decoction of rhizoma cimicifugae and radix puerariae by HPLC.[Methods] The separation of three active components were performed on a Waters XBridge column (250 mm×4.6 mm, 5 μm) by using an gradient mobile phase composed of CH3OH-0.05 mol/L KH2PO4, at acolumn temperature of 30℃, the flow rate was 0.8 mL/min, the detection wavelength was 230 nm and 317 nm.[Results] The peaks of paeoniflorin, puerarin and isoferulic acidcompletely resolved very well. The linear ranges of paeoniflorin, puerarin and isoferulic acid were 0.382~6.118 μg, 1.602~25.626 μg and 0.081~1.303 μg, the average recoveries(n=6) were 101.5%, 102.9% and 98.1% respectively, and the RSD was less than 3.0%.[Conclusion] This method is simple, accurate and repeatable. It can be used to simultaneously determine the content of the above three active compounds, as well as to provide a scientific basis for the quality evaluation of the decoction.
Key words:  decoction of rhizome cimicifugae and radix  HPLC  isoferulic acid  puerarin  paeoniflorin
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