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作 者:贾米兰[1] 陈丽[1] 李学兰[2] 赵应红 邱明丰[1]
机构地区:[1]上海交通大学药学院,上海200240 [2]中国医学科学院药用植物研究所云南分所,云南景洪666100 [3]西双版纳傣族自治州傣医医院,云南景洪666100
出 处:《中国民族医药杂志》2011年第11期39-41,共3页Journal of Medicine and Pharmacy of Chinese Minorities
基 金:云南省科技厅项目(2008IF018;2009BC014);上海市科委项目(08DZ1971303)资助
摘 要:目的:建立HPLC测定傣药肾茶中熊果酸含量的方法,研究不同产地肾茶中熊果酸含量的差异。方法:色谱柱为EclipseXDB-C_(18)(250mm×4.6mm,5μm),流动相为甲醇-0.5%乙酸铵(88:12),体积流量1.0mL/min,柱温为25℃,检测波长210nm,图谱采集时间为20min。结果:熊果酸与其他成分分离良好,在0.14~1.40μg范围内线性关系良好,r=0.9996,平均回收率为99.82%,RSD为0.79%(n=6)。结论:该法简便、准确可行,可用于傣药肾茶中熊果酸的含量测定及肾茶的质量控制,不同产地熊果酸含量有较大差异。Objective:To establish a HPLC method for the determination of ursolic acid in Dai Medicine - Orthosiphonari Status (Shencha),and compare the contents of different regions.Methods:Analyses were performed on Eclipse XDB-C18(250 mm×4.6 mm, 5μm) column with methanol-0.5%ammonium acetate system(88:12) as mobile phase at a flow rate of 1.0ml·min^(-1).The detection wave length was 210 run,column temperature was 25℃.Results:There is a good linearity between the amount range of 0.14~1.40μg(r= 0.9996).The average recovery was 99.82%and the RSD was 0.79%(n=6).Conclusion:The method is simple and accurate,which can be used to determine the contents of ursolic acid in Dai Medicine- Orthosiphonari Status(Shencha) and can be used for its quality control.The content of ursolic acid in Orthosiphonari Status from different regions is quite different.
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