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不同产地金银花与山银花主要成分的含量比较
引用本文:李红霞,王雪芹,李振国,刘乃强,范頔. 不同产地金银花与山银花主要成分的含量比较[J]. 中国药房, 2011, 0(31): 2935-2937
作者姓名:李红霞  王雪芹  李振国  刘乃强  范頔
作者单位:郑州大学附属肿瘤医院;河南省肿瘤医院;河南省食品药品检验所;河南科技大学动物科技学院;
基金项目:河南省科技攻关计划项目(102102310017)
摘    要:目的:比较不同产地金银花与山银花中主要成分含量的差异。方法:采用高效液相色谱(HPLC)-紫外扫描(UV)法测定不同产地金银花和山银花中绿原酸和木犀草苷的含量;采用HPLC-蒸发光散射检测器(ELSD)法测定2种药材中灰毡毛忍冬皂苷乙和川续断皂苷乙的含量。色谱柱为Agilent ZORBAX SB-C18(250mm×4.6mm,5μm),测定木犀草苷的流动相为乙腈-0.2%磷酸(梯度洗脱),流速为1.0mL·min-1,检测波长为350nm;测定绿原酸、灰毡毛忍冬皂苷乙和川续断皂苷乙的流动相为0.4%冰醋酸-乙腈(梯度洗脱),流速为1.0mL·min-1,绿原酸检测波长为324nm,其余两成分采用ELSD。结果:不同产地金银花中绿原酸、木犀草苷含量分别为2.227%~2.931%、0.0389%~0.0739%,不含灰毡毛忍冬皂苷乙和川续断皂苷乙;不同产地山银花中绿原酸含量为3.039%~5.657%,灰毡毛忍冬皂苷乙和川续断皂苷乙的总含量为5.59%~9.29%,不含木犀草苷,均符合现行版药典规定。结论:本试验结果可为金银花人工培育和GAP基地建设提供依据,同时为有效鉴别制剂中的金银花和山银花提供依据。

关 键 词:金银花  山银花  绿原酸  木犀草苷  灰毡毛忍冬皂苷乙  川续断皂苷乙  含量测定  比较  高效液相色谱法

Content Comparison of Main Compounds in Lonicera japonica and Flos Lonicerae from Different Producing Areas
LI Hong-xia WANG Xue-qin,LI Zhen-guo,LIU Nai-qiang FAN Di. Content Comparison of Main Compounds in Lonicera japonica and Flos Lonicerae from Different Producing Areas[J]. China Pharmacy, 2011, 0(31): 2935-2937
Authors:LI Hong-xia WANG Xue-qin  LI Zhen-guo  LIU Nai-qiang FAN Di
Affiliation:LI Hong-xia(The Affiliated Cancer Hospital of Zhengzhou University&Henan Provincial Tumor Hospital,Zhengzhou 450003,China) WANG Xue-qin,LI Zhen-guo,LIU Nai-qiang(Henan Province Institute for Food and Drug Control,China) FAN Di(School of Animal Science and Technology,Henan University of Science and Technology,Luoyang 471003,China)
Abstract:OBJECTIVE:To compare the difference of main compounds in Lonicera japonica and Flos Lonicerae from producing areas.METHODS:The contents of chlorogenic acid and galuteolin in L.japonica and Flos Lonicerae from producing areas were determined by HPLC-UV.The contents of macranthoidin B and dipsacoside B were determined by HPLC-ELSD.The Agilent ZORBAX SB-C18(250 mm×4.6 mm,5 μm) was adopted.The mobile phase consisted of acetonitrile-0.2% phosphoric acid(gradient elution) for galuteolin at flow rate of 1.0 mL·min-1 with detection wavelength of 350 nm.The mobile phase consisted of 0.4% glacial acetic acid-acetonitrile(gradient elution) for chlorogenic acid,macranthoidin B and dipsacoside B at the flow rate of 1.0 mL·min-1.The detection wavelength was set at 324 nm for chlorogenic acid,and the other was determined by ELSD.RESULTS:The contents of chlorogenic acid and galuteolin in L.japonica were 2.227%~2.931% and 0.038 9%~0.073 9%,excluding macranthoidin B and dipsacoside B;The total contents of macranthoidin B and dipsacoside B in Flos Lonicerae were 5.59%~9.29%.Galuteolin was not found.They were all in line with the standards stated in current pharmacopeia.The contents of chlorogenic acid were 3.039%~5.657%.CONCLUSION:The study provides references for artificial cultivation of L.japonica and GAP base construction,and it also provides basis for the identification of L.japonica and Flos Lonicerae.
Keywords:Lonicera japonica  Flos Lonicerae  Chlorogenic acid  Galuteolin  Macranthoidin B  Dipsacoside B  Content determination  Comparison  HPLC  
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