四川农业大学学报 ›› 2014, Vol. 32 ›› Issue (02): 154-159.doi: 10.3969/j.issn.1000-2650.2014.02.006

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金银花药材的HPLC指纹图谱及绿原酸、木犀草苷含量的同时测定

张芳1, 孙希芳1, 张永清1, 崔清华1, 于晓2,3   

  1. 1. 山东中医药大学药学院, 济南 250355;
    2. 山东大学药学院, 济南 250014;
    3. 山东医药技师学院, 山东 泰安 271016
  • 收稿日期:2014-03-17 出版日期:2014-06-30 发布日期:2017-02-28
  • 通讯作者: 张永清,教授,博士生导师,从事中药资源及其质量控制研究,E-mail:zyq622003@126.com。 E-mail:zyq622003@126.com
  • 作者简介:张芳,讲师,博士,从事中药资源及中药质量控制研究,E-mail:zfang_819@163.com。
  • 基金资助:
    国家十二五科技支撑计划课题(2011BAI06B01);山东省青年基金项目(ZR2011HQ057)

HPLC Fingerprints of Lonicerae japonica Flos and Determining the Chlorogenic Acid and Galuteolin Contents from Different Areas

ZHANG Fang1, SUN Xi-fang1, ZHANG Yong-qing1, CUI Qing-hua1, YU Xiao2,3   

  1. 1. College of Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan 250355, China;
    2. College of Pharmacy, Shandong University, Jinan 250014, China;
    3. Shandong Medicine Technician College, Taian 271016, Shandong, China
  • Received:2014-03-17 Online:2014-06-30 Published:2017-02-28

摘要: [目的] 建立金银花药材的HPLC指纹图谱,并同时测定不同产地商品中绿原酸和木犀草苷的含量,全面评价金银花药材质量。[方法] 采用Aglient TC-C18(4.6 mm×250 mm,5 μm)色谱柱。采用梯度洗脱,流动相A为1% HAC,流动相B为乙腈,洗脱程序为:0~5 min,A为95%→92%;5~7 min,A为92%→87%;7~28 min,A为87→85%;28~38 min,A为85→84%;38~43 min,A为84→82%;43~53 min,A为82→72%;53~63 min,A为72→50%;63~65 min,A为50→5%;75 min,A为5%。流速为0.8 mL/min;检测波长250 nm;柱温30℃。指纹图谱共有模式的建立采用国家药典委员会"中药色谱指纹图谱相似度评价系统2004A版"进行处理分析。[结果] 在指纹图谱研究中,标定了15个共有峰,建立了对照指纹图谱,10批药材与共有模式之间相似性良好,相似度均在0.9以上;在所建立的分析条件下,绿原酸、木犀草苷均达到了基线分离,且两者在线性范围内线性关系良好,两种成分的加样回收率分别为99.2%、99.4%。[结论] 本法灵敏、准确、简便,可用于金银花药材的综合质量评价。

关键词: 金银花, 指纹图谱, 绿原酸, 木犀草苷

Abstract: [Objective] This study established HPLC chromatographic fingerprint of Lonicerae japonica and measured the contents of chlorogenic acid and galuteolin from different areas.The objective was to comprehensively evaluate L. japonica quality. [Method] The Aglient TC-C18 column (4.6 mm×250 mm,5 μm) and gradient elution was used in this study.The mobile phase was composed of 1% HAC (A) and acetonitrile (B).The elution processes were shown as followed:0-5 mins,A 95%→92%;5-7 mins,A 92%→87%;7-28 mins,A 87→85%;28-38 mins,A 85→84%;38-43 mins,A 84→82%;43-53 mins,A 82→72%;53-63 mins,A 72→50%;63-65 mins,A 50→5%;75 min,A 5%.The flow rate was 0.8 mL/min.The detection wavelength was 250 nm and column temperature of 30℃.Data analysis was performed using professional software named Similarity Evaluation System for Chromatographic Fingerprint of Traditional Chinese Medicine composed by Chinese Pharmacopoeia Committee (Version 2004A). [Results] Fifteen common peaks were selected as fingerprints of L. japonica there were good similarities (>0.9)between standard fingerprint and the fingerprint from 10 medicinal materials.Underthe established conditions,the chlorogenic acid and galuteolin were separated well.Additionally,all calibration curves showed good linear regression and their recovery were 99.2% and 99.4%,respectively. [Conclusion] The method is sensitive,accurate and convenient and it can be used to evaluate L. japonica quality.

Key words: Lonicerae japonica, fingerprint, chlorogenic acid, galuteolin

中图分类号: 

  • R284.1