天然产物研究与开发 ›› 2017, Vol. 29 ›› Issue (5): 810-814.doi: 10.16333/j.1001-6880.2017.5.016

• 研究简报 • 上一篇    下一篇

甘草干姜汤中8种药效组分的含量测定

杨颜芳1,张贵君1,2*,王晶娟1,孙启玉2,刘亮2,彭慧2,向丽1   

  1. 1 北京中医药大学,北京100102;2淄博万杰中医药研究所,淄博 255000
  • 出版日期:2017-05-31 发布日期:2017-06-09

Determination of 8 Active Components in Gancao-Ganjiang-Tang by High-Performance Liquid Chromatography

YANG Yan-fang1,ZHANG Gui-jun1,2*,WANG Jing-juan1,SUN Qi-yu2,LIU Liang2,PENG Hui2,XIANG Li1   

  1. 1 Department of Pharmacognosy,Beijing University of Chinese Medicine,Beijing 100102,China;  2 Zibo Wanjie Institute of Chinese medicine,Zibo 255000,China
  • Online:2017-05-31 Published:2017-06-09

摘要: 分析测定不同本草所载甘草干姜汤中的8种药效组分,为其建立与临床疗效相对应的质量标准提供技术和思路。甘草干姜汤按照传统煎煮方法制备,用高效液相色谱(HPLC)对其药效组分进行测定。流动相(A)0.1%磷酸水溶液-(B)乙腈,梯度洗脱(0~5 min,5%~15%B;5~10 min,15%~22%B;10~15 min,22%~26%B;15~30 min,26%~28%B;30~32 min,28%~55%B;32~35 min,55%~60%B;35~40 min,60%~63%B;40~45 min,63%~65%B),流速0.6 mL/min,柱温30 ℃。所得不同甘草干姜汤中的8种药效组分(甘草苷、异甘草苷、甘草素、甘草酸、异甘草素、6-姜酚、8-姜酚、6-姜烯酚)含量分别为175.68、20.23、10.87、367.79、1.99、2948、9.93、4.88 μg/mL(炙甘草12 g干姜6 g);243.14、29.87、14.97、624.53、3.29、22.42、14.97、3.14 μg/mL(炙甘草12 g-炮干姜6 g);151.42、17.45、8.92、344.03、1.52、24.2、7.17、0.84 μg/mL(炙甘草9 g-炮干姜9 g)。本实验所采用的HPLC法快速、可靠,所测得的8种药效组分可作为甘草干姜汤质量控制的科学指标,也为建立与临床疗效相对应、安全、有效、稳定的中药质量评价体系提供一个新方向。

关键词: 甘草干姜汤, 临床疗效, 质量控制, 药效组分

Abstract: Gancao-Gangjiang-Tang(GGT) is a Traditional Chinese medicine(TCM) Prescription and is a representative prescription for recuperating depleted Yang in Treatise on Febrile Diseases. The TCM theory believes that the efficacy of medicinal herbs is decided by the multicompounds which consist of different kinds of chemical constituents with bioactivities,but not by a monomeric constituent. To determine 8 active compositions alignment in GGT so as to provide technology and ideas for the establishment of quality standard in accordance with its therapeutic effects,a new TCM(including single herb and prescription) quality control method is proposed. A high-performance liquid chromatography(HPLC) was established for the simultaneous determination of 8 compounds in GGT. The analysis was performed on a Hypersil Gold-C18 (4.6 mm×250 mm,5 μm) column at a flow rate of 0.6 mL/min. The mobile phase consisted of acetonitrile(A) and 0.1% H3PO4 aqueous(B) using a gradient elution of 5%-15%A at 0-5 min,15%-22%A at 5-10 min,22%-26%A at 10-15 min,26%-28%A at 15-30 min,28%-55%A at 30-32 min,55%-60%A at 32-35 min,60%-63%A at 35-40 min,and 63%-65%A at 40-45 min. The column temperature was holding on 30 ℃. The total contents of the 8 compounds in different GGT varied from 555.56 to 956.33 μg/mL,and the composition of them were also varied. The results showed that the dosage and compatibility of medicinal herbs have influenced the content of chemical compounds of TCM Prescription while the content of chemical compounds have act on clinical efficacy. Quality evaluation and active essence screening of TCM should be based on the TCM theory and clinical effectiveness. The method was applied to the simultaneous determination of eight compounds in GGT and was proven to be suitable for quality evaluation of GGT.

Key words: Gancao-Gangjiang-Tang, clinical effectiveness, TCM quality control, multicompounds