HPLC测定野马追中野马追内酯A,B和金丝桃苷的含量  被引量:2

Determination of Eupalinolide A,B and Hyperin in Eupatorium Lindleyanum DC by HPLC

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作  者:罗敏敏[1] 李春华[1] 王易芬[2] 

机构地区:[1]中南大学化学化工学院,长沙410083 [2]中国科学院昆明植物所,昆明650201

出  处:《中国现代应用药学》2012年第11期1018-1022,共5页Chinese Journal of Modern Applied Pharmacy

摘  要:目的采用高效液相色谱法对不同产地的6批野马追药材中野马追内酯A,B和金丝桃苷进行了定性定量分析。方法野马追内酯A,B的测定采用AgilentExtend.C18(4.6mm×150mm,5μm)为分析柱,乙腈-水(27:73)为流动相,流速为1.0mL·min-1,等度洗脱,检测波长为220nm,柱温为30℃。金丝桃苷的测定以SB—C18为分析柱,乙腈-1%醋酸水溶液(12:88)为流动相,流速为1.0mL·min-1,等度洗脱,检测波长为255nm。结果野马追内酯A在0.02-1.88μg,野马追内酯B在0.44~4.44μg内与峰面积呈良好的线性关系。金丝桃苷在0.101~1.414μg内与峰面积呈良好的线性关系。结论本实验方法准确、快速、灵敏、重复性好,在该色谱条件及样品处理方法下,可以准确测定野马追中野马追内酯A,B和金丝桃苷的含量。OBJECTIVE To establish a method for the determination of the content of eupalinolide A, B and hyperin in Eupatorium lindleyanum DC from 6 different areas by HPLC. METHODS For eupalinolide A, B, Agilent Extend-Cl8 column (4.6 mm×150 mm, 5μm) was used under the mobile phase of acetonitrile-water(27 : 73) at the flow rate of 1.0 mL min-1. The detection wavelength was 220 nm and the column temperature was maintained at 30 ℃. For hyperin, SB-CI8 column was used under the mobile phase of acetonitrile-1% Acetic acid(12 : 88) at a flow of 1.0 mL,min-L The detection wavelength was 255 nm and the column temperature was maintained at 30 ℃. RESULTS The standard curve of eupalinolide A was linear in the range of 0.02-1.88 μg and eupalinolide B was linear in the range of 0.44-4.44 μg. The standard curve of hyperin was linear in the range of 0.101-1.414 μg. CONCLUSION This method was simple, accurate and reproducible for the determination of eupalinolide A, B and hyperin in Eupatorium lindleyanum DC.

关 键 词:野马追 野马追内酯A 野马追内酯B 金丝桃苷 高效液相色谱法 

分 类 号:R917.101[医药卫生—药物分析学]

 

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