HPLC同时测定枸骨叶中熊果酸和齐墩果酸的含量  被引量:4

Determination of Ursolic Acid and Oleanolic Acid in Ilicis Cornutae Folium by HPLC

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作  者:施之琪[1] 王洛临[1] 曾文雪[2] 付建武[3] 

机构地区:[1]广东省中医研究所,广州510095 [2]江西中医学院,南昌330006 [3]广州中医药大学,广州510405

出  处:《江西中医学院学报》2013年第1期58-60,共3页Journal of Jiangxi College of Traditional Chinese Medicine

摘  要:目的:建立枸骨叶药材中熊果酸、齐墩果酸的含量测定方法。方法:采用高效液相色谱法,色谱柱:Extend-C18(4.6mm×250mm,5μm),流动相:甲醇-0.1moL L-1醋酸铵溶液(83 17),流速为1.0mL min-1,柱温30℃,检测波长210nm。结果:熊果酸在23.6-236.0μg mL-1线性关系良好(r=0.999 9),平均回收率为98.84%,RSD为0.75%。齐墩果酸在10.42-104.20μg mL-1线性关系良好(r=0.999 9),平均回收率为98.87%,RSD为1.00%。结论:该方法简单,准确,且专属性强,可作为枸骨叶药材质量控制方法。Objective: HPLC method was established for determination of ursolic acid and oleanolic acid in Ilicis Cornutae Folium. Method: HPLC was carried out on Extend-C 18(4.6mm×250mm,5μm) at 30℃ using methanol-0.1 moL . L-1 ammonium acetate(83:17) as mobile phase with a flow rate of 1.0 mL . min^- and detection wavelength was at 210nm.Result: Linear correlation(r=0.9999) of the peak area and the concentration of ursolic acid over the concentration range 23.6-236.0μg . mL^-1 was obtained.Linear correlation(r=0.999 9)of the peak area and the concentration of oleanolic acid over the concentration range 10.42-104.20μg . mL^- was obtained. The average recovery was 98.84%,98.87% and RSD was 0.75%,1.00%.Conclusion: The method is simple,rapid and accurate. It can be used for the quality control of Ilicis Cornutae Folium.

关 键 词:枸骨叶 熊果酸 齐墩果酸 高效液相色谱法 

分 类 号:R284.1[医药卫生—中药学]

 

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