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作 者:韩永成[1] 刘伟[1] 陈宁[1] 崔永霞[1] 黄丽杰[1]
出 处:《天然产物研究与开发》2015年第1期89-93,共5页Natural Product Research and Development
基 金:河南省教育厅自然科学研究计划项目(2010A360016)
摘 要:本实验建立了UHPLC同时测定不同产地金银花中绿原酸、芦丁、木犀草苷、异绿原酸A、异绿原酸B、异绿原酸C含量的分析方法。采用Agilent 1290超高效液相色谱系统,Agilent ZORBAX RH C18色谱柱(50 mm×2.1 mm,1.8μm),流动相为乙腈-0.2%磷酸水,以0.2 m L/min的流速进行梯度洗脱,柱温30℃,检测波长350nm。结果表明在该色谱条件下,金银花的6种有效成分在8 min内可达到基线分离。方法的加样回收率为96.88%~99.16%,相对标准偏差为0.23%~1.06%。UHPLC法分析速度快,重复性好,结果准确,可用于金银花中绿原酸、芦丁、木犀草苷、异绿原酸A、异绿原酸B、异绿原酸C的含量测定。To establish an UHPLC method for simultaneous determination of six compounds,namely chlorogenic acid,rutin,luteoloside,3,5-O-dicaffeoylquinic acid,3,4-O-dicaffeoylquinic acid and 4,5-O-dicaffeoylquinic acid in Lonicera japonica Thunb from different areas. The chromatographic separation was performed on an Agilent ZORBAX RH C18(50 mm × 2. 1 mm,1. 8 μm) column with gradient elution. The flow rate was 0. 2 m L/min. The column temperature was 30 oC. The detection wavelength was 350 nm. The recoveries of rutin,luteoloside and four kinds of organic acids were96. 88%-99. 16%,and the relative standard deviations were 0. 23%-1. 06%. The developed UHPLC method was reproducible,accurate and efficient. It can be used for the simultaneous detection and determination of chlorogenic acid,rutin,luteoloside,3,5-O-dicaffeoylquinic acid,3,4-O-dicaffeoylquinic acid,4,5-O-dicaffeoylquinic acid in L. japonica.
关 键 词:金银花 UHPLC 绿原酸 芦丁 木犀草苷 异绿原酸A 异绿原酸B 异绿原酸C
分 类 号:R917[医药卫生—药物分析学]
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