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四川紫金牛属药用植物的黄酮类活性组分的含量分析
引用本文:汤昊,何海洋,宋良科,董关涛,王小宁,王岩.四川紫金牛属药用植物的黄酮类活性组分的含量分析[J].特产研究,2011,33(3):48-51.
作者姓名:汤昊  何海洋  宋良科  董关涛  王小宁  王岩
作者单位:1. 西南交通大学生命科学与工程学院,成都,610031
2. 西安交通大学医学院,西安,710061
基金项目:国家科技部平台项目(2005DKA2100)
摘    要:用高效液相色谱法分析四川紫金牛属7种2变种药用植物的黄酮类活性组分,拟比较种与种间、同种不同入药部位之间的杨梅素、山奈酚和槲皮素的含量差异,探索紫金牛属植物的亲缘关系与药用组分含量的相关性,为紫金牛属不同药材质量控制标准的建立提供实验依据。色谱柱为Symmetry C18(4.6mm×250mm,5μm);流动相为甲醇:0.04%的磷酸溶液(50:50);体积流量:0.8mL/min;检测波长:368nm;柱温:30%;进样量10μL。杨梅素、槲皮素、山奈酚获得良好基线分离,线性回归方程分别为Y=36231X-133956,r=0.9996;Y=45758X-53050,r=0.9995;Y=27569X-7263.5,r=0.9996;线性范围分别为0.064μg-1.920μg,0.084μg-2.522μg,0.061μg~1.841μg;回收率分别为98.19%、97.88%、99.58%;RSD均小于1.6%;四川紫金牛属7种2变种药用植物均含有杨梅素、山奈酚、槲皮素。在相同条件下圆齿组植物的槲皮素含量均高于锯齿组植物;同种不同人药部位中,叶的黄酮类各组分含量远高于根、茎;百两金及其变种大叶百两金的山奈酚含量远高于其他种,其叶含量达6.42~9.13mg/g,可作为山奈酚资源植物加以利用。

关 键 词:紫金牛属  黄酮类  HPLC  分析

Analysis of the Active Components Flavonoid Content in Sichuan Ardisia Medicinal Plants
TANG Hao,HE Hai-yang,SONG Liang-ke,DONG Guan-tao,WANG Xiao-ning,WANG Yan.Analysis of the Active Components Flavonoid Content in Sichuan Ardisia Medicinal Plants[J].Special Wild Economic Animal and Plant Research,2011,33(3):48-51.
Authors:TANG Hao  HE Hai-yang  SONG Liang-ke  DONG Guan-tao  WANG Xiao-ning  WANG Yan
Institution:TANG Hao1,HE Hai-yang2,SONG Liang-ke1,DONG Guan-tao1,WANG Xiao-ning1,WANG Yan1(1.Life Science and Engineering College,Southwest Jiaotong University,Chengdu 610031,China,2.Medical College,Xi-an Jiaotong University,Xi-an 710061,China)
Abstract:Based on analyzing results of the active components flavonoid content in Sichuan Ardisia medicinal plants,to compare the flavonoid content differences among species and different part of the same plant;to explore the relativity of genetic relationship among species in Ardisia and the content of three types of flavonoid;and to offer some experimental evidences for establishing quality control standard of medical herbs from Ardisia.The HPLC was performed using Symmetry C18 column(4.6mm×250mm,5μm) and methanol-water(50:50) as the mobile phase.The flow rate was 0.8mL/min,the detection wavelength was 368nm,and the column temperature was 30℃.The external standard method was used to carrying out quantitative analysis.The regression equation of myricetin,quercetin and kaempferol was separately Y=36 231X-133 956,r=0.999 6;Y=45 758X-53 050,r=0.999 5;Y=27 569X-7 263.5,r=0.999 6.The linear range was 0.064~1.920,0.084~2.522,0.061~1.841μg respectively;the average recovery was 98.19%,97.88%,99.58% respectively.RSD was all less than 1.6%.And there are myricetin,quercetin and kaempferol in all these 7 species and 2 subspecies.Under the same condition,the amount of quercetin in plants of Ardisia sect.Crispardisia is higher than that of sect.Bladhia;the amount of myricetin,quercetin and kaempferol in leaves was much higher than those in stems and roots.The amount of kaempferol of A.crispa and A.crispa var.amplifolia,which was up to 6.42~9.13mg/g,was much higher than all other species;so it is recommended that these two species should be used as the resource plants of kaempferol.
Keywords:Ardisia  Flavonoid  HPLC  Analysis  
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