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机构地区:[1]甘肃省兰州大学药学院,兰州730000 [2]甘肃省药品检验研究院,甘肃省中药品质与安全评价工程技术研究中心,兰州730000
出 处:《中国实验方剂学杂志》2015年第8期81-85,共5页Chinese Journal of Experimental Traditional Medical Formulae
摘 要:目的:建立HPLC测定烈香杜鹃中芦丁、金丝桃苷、槲皮苷、槲皮素、山柰酚和异鼠李素6种黄酮成分的方法,同时应用主成分分析评价其质量。方法:样品经75%甲醇超声,采用C18色谱柱(4.6 mm×250 mm,5μm),乙腈-0.2%磷酸水为流动相梯度洗脱,流速1.0 m L·min^-1,检测波长365 nm。结果:芦丁,金丝桃苷,槲皮苷,槲皮素,山柰酚,异鼠李素在0.009 7-0.194 9,0.007 1-0.141 6,0.188 0-3.752,0.027 1-0.434 0,0.010 8-0.216 0,0.005 8-0.116 6μg线性范围良好,加样回收率均在100%-105%,RSD都〈3%。结论:HPLC操作简便、重复性好、结果准确。根据不同化学指标,采用主成分分析可以进行烈香杜鹃质量评价。Objective: To establish an HPLC method for the determination of rutin, hyperoside, quercitrin, quercetin, kaempferol and isorhamnetin in Rhododendron anthopogonoides, while using principal component analysis to evaluate its quality. Method: Samples were extracted with 75% methanol by ultrasound. The separation was performed on a C18 column (4.6 mm×250 mm,5μm) with acetonitrile-0.2% HaPO4 as mobile phase in a gradient elution. The flow rate was 1.0 mL ·min^-1, the wavelength was set at 365 nm. Result: Rutin, hyperoside, quercitrin, quercetin, kaempferol, and isorhamnetin have good linearity in the range of 0. 009- 0.1949, 0.007 1-0.141 6, 0.0.188 0-0.375 2, 0.027 1-0.434 0, 0.010 8-0.216 0, 0.005 8-0.116 6 μg, respectively. The recoveries were 100%-105% , RSD were 〈 3%. Conclusion: The established HPLC method was simple, accurate, reproducible, and reliable. Depending on the chemical indicators, using principal component analysis can be carried out quality assessment for R. anthopogonoides.
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