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作 者:龚健[1] 卢帅[1] 索菲娅[1] 王傲立[1] 叶星[1]
机构地区:[1]新疆大学生命科学与技术学院,乌鲁木齐830046
出 处:《中国实验方剂学杂志》2014年第11期50-52,共3页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家自然科学基金项目(31160073);新疆维吾尔自治区教育厅项目(XJEDU2010I12);新疆维吾尔自治区科技厅项目(201091245)
摘 要:目的:建立HPLC测定新疆产短星火绒草中绿原酸和咖啡酸含量的方法,并用于短星火绒草中绿原酸和咖啡酸含量的测定。方法:采用Diamonsil“(钻石)C18色谱柱(4.6mm×250mm,5μm),流动相乙腈-0.5%磷酸溶液(10:90),流速1.0mL·min^-1,柱温40℃,检测波长280nm。结果:绿原酸线性范围0.08~0.76μg(r=0.9999),平均加样回收率99.48%,RSD2.82%。咖啡酸线性范围0.051~0.459μg(r=0.9999),平均加样回收率100.31%,RSD0.96%。结论:该法简单、准确、重复性好,可用于测定短星火绒草中绿原酸和咖啡酸含量。Objective: To establish high performance liquid chromatography (HPLC) method for the determination of chlorogenic acid and caffeic acid in Leontopodium brachyactis from Xinjiang for the first time. Method: The stationary phase was DiamonsilTM Cls (4.6 mm× 250 mm, 5μm)column and the mobile phase was acetonitrile-0. 5% phosphoric acid ( 10: 90). The flow rate was maintained at 1.0 mL ·min^-1 and the column temperature was set at 40 ℃. The detective wavelength was set at 280 nm. Result: The liner range of chlorogenic acid was 0.08-0. 76 μg (r = 0. 999 9). The average recovery was 99.48% ( RSD 2.82% ). The liner range of caffeic acid was 0.051-0.459 μg (r = 0.999 9). The average recovery was 100.31% ( RSD 0.96%). Conclusion: The method is simple, accurate and sensible, and can be used to determine the content of the chlorogenic acid and caffeic acid in L. brachyactis.
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