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机构地区:[1]中国医学科学院北京协和医学院药用植物研究所,北京100094 [2]卫生部北京医院药学部临床药理室,北京100730
出 处:《中国新药杂志》2008年第18期1600-1602,1621,共4页Chinese Journal of New Drugs
基 金:国家自然科学基金(30772711);公益性科研院所基本科研业务专项资金(YZ-1-26)
摘 要:目的:建立高效液相色谱法测定枳壳饮片中柚皮芸香苷、柚皮苷、橙皮苷和新橙皮苷的含量。方法:采用Sunfire C18色谱柱(150 mm×4.6 mm,5μm),以乙腈-0.1%磷酸溶液(20∶80)为流动相,流速为1 mL.min^-1,检测波长为283 nm,柱温为30℃。结果:柚皮芸香苷、柚皮苷、橙皮苷和新橙皮苷分别在0.074-123.7,0.60-999.0,0.072-120.3和0.59-982.0μg.mL^-1范围内线性良好,其平均回收率分别为96.6%,96.1%,96.0%和97.2%。结论:该方法简便、快速、准确、重复性好,可用于枳壳中柚皮芸香苷、柚皮苷、橙皮苷和新橙皮苷的同时测定。Objective:To establish a HPLC method for simultaneous determination of narirutin, naringin, hesperidin and neohesperidin in Citrus aurantium L. Methods:The HPLC analysis was performed on a Sunfire Cl8 (150 mm× 4.6 mm,5 μm)column. The column temperature was set at 30 ℃. A mixture of aeetonitrile-0. 1% phosphoric acid aqueous solution(20: 80)was used as the mobile phase with the flow rate at 1 mL-min^-1. The detection wavelength was set at 283 nm. Results:Good linearity was obtained in the ranges of 0. 074 -123.7 μg.mL^-1, 0.60 - 999.0 μg.mL^-1 , 0. 072 - 120.3 μg. mL^-1 , and 0.59 - 982.0 μg.mL^-1 with average recoveries of 96.6% ,96. 1% ,96.0% and 97.2% for narirutin, naringin, hesperidin and neohesperidin, respectively. Conclusion:The method is simple, rapid, accurate and reproducible for simultaneous determination of narirutin, naringin, hesperidin and neohesperidin in Citrus aurantium L.
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