今天是:   返回主页   |   加入收藏   |   联系我们
引用本文:
【打印本页】   【HTML】   【下载PDF全文】   查看/发表评论  下载PDF阅读器  关闭
←前一篇|后一篇→ 过刊浏览    高级检索
本文已被:浏览 1532次   下载 1105 本文二维码信息
码上扫一扫!
分享到: 微信 更多
芍药-甘草不同配伍比例提取物中有效成分溶出规律的研究
刘秀琨1, 陈颖1, 冉棋1, 赵卓卓1, 李纳纳1, 丁辉2, 余河水1, 李薇1, 孟凡英1, 宋新波1,2
1.天津中医药大学, 中药制药工程市级实验教学示范中心, 天津 301617;2.天津中一制药有限公司, 天津 300193
摘要:
[目的]通过测定不同比例芍药-甘草药对提取液的pH值、密度、出膏率和6种有效成分的含量综合探讨相关指标随芍药-甘草药对配伍变化规律,探究芍药-甘草药对的质量标志物。[方法]分别测定出膏率、pH值、密度;采用Kromasil 100-5-C18色谱柱(250 mm×4.6 mm,5 μm),流动相为乙腈(B)-0.1%磷酸水溶液(A),梯度洗脱(0~8 min,14%~19% B;8~20 min,19%~28% B;20~25 min,28%~35% B;25~30 min,35%~45% B;30~40 min,45%~95% B,流速1.0 mL/min,检测波长为254 nm,柱温30℃。[结果]芍药-甘草不同比例(1∶0、10∶1、10∶2、10∶3、10∶4、10∶5、10∶6、10∶7、10∶8、1∶1、1∶2、1∶3、1∶4、1∶6、1∶8、0∶1)提取液的密度和pH值与比例大小没有明显关系,密度变化范围为1.003±0.002,pH密度变化范围为4.94±0.11,出膏率变化范围为15.39±1.70。芍药-甘草不同比例组煎煮过程中,芍药中芍药内酯苷和芍药苷的变化趋势较为接近,甘草中甘草苷和甘草酸的变化趋势相近。[结论]综合不同比例芍药-甘草药对提取液的pH值、密度、出膏率和6种有效成分的含量结果,从化学成分层面上,选择芍药内酯苷、芍药苷、甘草苷和甘草酸作为芍药-甘草药对的质量标志物科学合理。
关键词:  芍药-甘草  配伍比例  有效成分溶出率
DOI:10.11656/j.issn.1673-9043.2019.05.18
分类号:R283
基金项目:天津市科技计划项目(17JCTPJC49700,18JCT-PJC64600)。
Study on the dissolution rules and quality markers of active components in the extracts of paeonia-liquorice with different compatibility ratios
LIU Xiukun1, CHEN Ying1, RAN Qi1, ZHAO Zhuozhuo1, LI Nana1, DING Hui2, YU Heshui1, LI Wei1, MENG Fanying1, SONG Xinbo1,2
1.Tianjin University of Traditional Chinese Medicine, Municipal Experimental Teaching Demonstration Center of Traditional Chinese Medicine Pharmaceutical Engineering, Tianjian 301617, China;2.Tianjin Zhongyi Pharmaceutical Co. Ltd., Tianjin 300193, China
Abstract:
[Objective] By measuring the ratio of pH value,density,ointment rate,polysaccharide content and content of six active ingredients in different proportions of shaoyao-gancao decoction,the related indexes were studied with the variation of the compatibility change law,and exploring the quality markers of shaoyao-gancao pairs.[Methods] To determinate the paste rate,the ratio of pH value and density,separately. The determination was carried out with Kromasil 100-5-C18 column (250 mm×4.6 mm,5 μm). The mobile phase consisted of acetonitrile (B)-0.1% phosphoric acid aqueous solution (A) with gradient elution manner (0~8 min,14%~19%B,8~20 min, 19%~28% B,20~25 min,28%~35% B,25~30 min,35%~45% B,30~40 min,45%~95% B). The flow rate was 1.0 mL/min,the detection wavelength was 254 nm and the column temperature was 30℃.[Results] There was no significant relationship between the density and the pH value of the extract and the ratio (1:0,10:1,10:2,10:3,10:4, 10:5,10:6,10:7,10:8,1:1,1:2,1:3,1:4,1:6,1:8,0:1). The range of density change was 1.003±0.002,the range of pH change was 4.94±0.11,and the range of paste rate change was 15.39±1.70. In the decoction process of different proportions of shaoyao-gancao,the change trend of albiflorin and paeoniflorin in shaoyao was similar,and the change trend of liquiritin and glycyrrhizic acid in gancao was similar.[Conclusion] According to the results of different ratios of shaoyao-gancao extract pH,density,paste rate and content of six active ingredients. From the chemical composition level,it is scientific and reasonable to choose albiflorin,paeoniflorin,liquiritin and glycyrrhizic acid as the quality marker of shaoyao-gancao.
Key words:  shaoyao-gancao  compatibility ratio  active ingredient dissolution rate
关注公众号二维码