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芍药与甘草配伍协同增效作用的物质基础研究
引用本文:王君,戴丽,李鹏跃,霍海如,隋峰,张春凤,李兰芳,郭淑英,李沧海,姜廷良.芍药与甘草配伍协同增效作用的物质基础研究[J].中国实验方剂学杂志,2014,20(11):83-86.
作者姓名:王君  戴丽  李鹏跃  霍海如  隋峰  张春凤  李兰芳  郭淑英  李沧海  姜廷良
作者单位:中国药科大学, 南京 211198;中国药科大学, 南京 211198;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;中国中医科学院中药研究所, 北京 100700;中国药科大学, 南京 211198;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;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
基金项目:国家自然科学基金项目(30873393,81274112);北京市自然科学基金项目(7112098);中国中医科学院传承项目(CM20123002)
摘    要:目的:探讨芍药与甘草配伍增效的化学物质基础。方法:芍药和甘草中主要活性成分采用HPLC检测;对方法学进行了专属性、线性范围、精密度、稳定性、重复性、加样回收率等考察。结果:芍药单味药单煎后芍药苷检测到的含量为2.19 mg·g-1;甘草单味药单煎后甘草酸检测到的含量为17.13 mg·g-1;芍药和甘草分别单煎再按1∶1混合,芍药苷检测到的含量为5.45 mg·g-1,甘草酸检测到的含量为17.69 mg·g-1;芍药和甘草按1∶1混合煎煮,芍药苷检测到的含量为2.58 mg·g-1,甘草酸检测到的含量为18.14 mg·g-1。结论:芍药与甘草配伍,两药单煎混合芍药苷和甘草酸的含量均显著提高,但前者增高更为明显;两药混合煎煮,芍药苷和甘草酸的含量均明显提高,但以后者更为显著;芍药与甘草配伍止痛的科学基础可能与两药合用后的芍药苷和甘草酸的含量增高有关。

关 键 词:芍药  甘草  配伍  物质基础
收稿时间:2013/12/15 0:00:00

Study on Active Ingredients for Increased Efficacy of Compatibility of Penoy and Licorice
WANG Jun,DAI Li,LI Peng-yue,HUO Hai-ru,SUI Feng,ZHANG Chun-feng,LI Lan-fang,GUO Shu-ying,LI Cang-hai and JIANG Ting-liang.Study on Active Ingredients for Increased Efficacy of Compatibility of Penoy and Licorice[J].China Journal of Experimental Traditional Medical Formulae,2014,20(11):83-86.
Authors:WANG Jun  DAI Li  LI Peng-yue  HUO Hai-ru  SUI Feng  ZHANG Chun-feng  LI Lan-fang  GUO Shu-ying  LI Cang-hai and JIANG Ting-liang
Institution:College of Traditional Chinese Medicine, China Pharmaceutical University, Nanjing 211198, China;College of Traditional Chinese Medicine, China Pharmaceutical University, Nanjing 211198, China;Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China;Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China;Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China;College of Traditional Chinese Medicine, China Pharmaceutical University, Nanjing 211198, China;Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China;Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China;Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China;Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China
Abstract:Objective:To explore the chemical basis for co-application of Paeonia lactiflora and Glycyrrhizae uralensis. Method:The contents of peoniflorin and glycyrrhizin were detected by using the method of high-performance liquid chromatography (HPLC) and the test methods in terms of specificity, linear range, precision, stability, repeatability and sample recovery were performed to determine the optimum chromatographic conditions. Result:The content of peoniflorin in P. lactiflora decoction was 2.19 mg·g-1; the content of glycyrrhizin in G.uralensis was 17.13 mg·g-1; the contents of peoniflorin and glycyrrhizin were 5.45, 17.69 mg·g-1 respectively when P. lactiflora and G. uralensis were mixed together after decocting the component herbs singly; the contentsof peoniflorin and glycyrrhizin were 5.45, 17.69 mg·g-1 respectively when P. lactiflora and G. Uralensis were decocted together. Conclusion:The contents of peoniflorinand glycyrrhizinwere promoted significantly with the former more significant when the component herbs were decocted singly and the contents of peoniflorinand glycyrrhizin was elevated greatly with the latter more significant when the component herbs were decocted together; the increase in contents of peoniflorinand glycyrrhizin may compose one of important reasons behind the synegetic analgesic potency when P. lactiflora and G. uralensis are used together.
Keywords:Paeonia lactiflora  Glycyrrhizae uralensis  compatibility  material basis
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