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作 者:卫阳飞[1] 戚欢阳[2] 宋海[1] 岳国仁[1]
机构地区:[1]河西学院甘肃省河西走廊特色资源利用重点实验室,甘肃张掖734000 [2]中国科学院兰州化学物理研究所,兰州730000
出 处:《中国实验方剂学杂志》2015年第12期36-39,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家自然科学基金项目(21462016);河西学院青年教师科研基金项目(QN2014-15)
摘 要:目的:建立双波长HPLC同时测定金刚藤软胶囊中绿原酸、白藜芦醇、芦丁、槲皮素和山柰酚含量的方法。方法:采用Agilent ZORBAX SB-C18色谱柱(4.6 mm×150 mm,5μm),流动相乙腈-0.1%磷酸水溶液梯度洗脱,流速1.0 m L·min^-1,柱温25℃,检测波长306 nm(绿原酸、白藜芦醇)和365 nm(芦丁、槲皮素、山柰酚)。结果:绿原酸、白藜芦醇、芦丁、槲皮素、山柰酚分别在0.058 5~2.34μg(r=0.999 8),0.025 3~1.01μg(r=0.999 9),0.042 2~0.844μg(r=0.999 6),0.018 1~0.722μg(r=0.999 9),0.0165~0.660μg(r=0.999 9)呈现良好的线性关系,平均回收率分别为98.0%,100.6%,96.0%,102.7%,98.5%,RSD分别为1.2%,2.2%,1.8%,2.9%,1.3%。结论:该方法操作简便、重复性好,可作为金刚藤软胶囊中5个活性成分的含量测定方法。Objective: To establish a dual-wavelength HPLC method for simultaneous determination of five constituents (chlorogenic acid, resveratrol, rutin, quercetin, kaempferol) in Jingangteng soft capsule. Method: The Agilent ZORBAX SB-Cls column (4.6 mm× 150 mm, 5μm) with a column temperature of 25℃ was used; the mobile phase was acetonitrile-0. 1% phosphoric acid at gradient elution program and with a flow rate of 1.0 mL· min^-1, and the detection wavelengths were set at 306 nm ( chlorogenic acid and resveratrol) and 365 nm (rutin, quercetin and kaempferol). Result: The linear response ranges of chlorogenic acid, resveratrol, rutin, quercetin, and kaempferol were 0. 058 5-2.34μg (r = 0. 999 8) , 0. 025 3-1.01μg (r = 0. 999 9) , 0. 042 2- 0.844 μg (r = 0.999 6), 0.018 1-0.722μg (r = 0.999 9), and 0.016 5-0. 660 μg (r = 0.999 9), respectively. The average recoveries were 98.0% , 100.6% , 96.0% , 102.7% , and 98.5% with RSDs of 1.2% , 2.2% , 1.8% , 2.9% , and 1.3% , respectively. Conclusion: The developed method was convenient and reliable, which could be applied to determination of five effective constituents in Jinggangteng soft capsule.
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