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作 者:杨月娥[1] 朱恩焕[1] 胡文[1] 袁云[1] 马兴芬[1] 刘德举[1]
出 处:《中国实验方剂学杂志》2013年第5期120-122,共3页Chinese Journal of Experimental Traditional Medical Formulae
基 金:大理市科技局科研基金资助项目(2008SF11)
摘 要:目的:建立同时测定鸡肉参中芦丁、槲皮苷、槲皮素含量的HPLC-DAD方法。方法:采用Diamonsil-C18色谱柱(150 mm×4.6 mm,5.0μm),柱温30℃,以甲醇(A)-0.5%磷酸水溶液(B)为流动相,进行梯度洗脱(0~5 min,48%~52%A;6~10 min,70%~30%A),检测波长254 nm,流速1.0 mL.min-1。结果:3种黄酮类成分在10 min内达到良好分离,芦丁、槲皮苷、槲皮素的线性范围分别为0.3~1.0 mg(r=0.999 8),0.030~0.10 mg(r=0.999 8),0.010~0.033 mg(r=0.999 5);平均加样回收率分别为100.95%(RSD 0.98%),99.51%(RSD 1.54%),102.84%(RSD 3.53%)。结论:该方法简便,快速,精确,可同时测定鸡肉参中芦丁、槲皮苷、槲皮素的含量,具有较好的重复性和稳定性,可作为鸡肉参药材的质量控制方法。Objective:To establish an HPLC-DAD method for simultaneous determination of rutin, quercetin and quercitroside in Incarvillea mairei. Method: A Dikma Diamonsil C18column (4.6 mm×150 mm, 5 μm) was used. The column temperature was set at 30 ℃; the investigated compounds were separated with gradient mobile phase consisting of methanol (A)-0.5% phosphoric acid (B); the flow rate was 1.0 mL·min-1 and the detection wavelength was kept at 254 nm. Result: The good separation of three flavonoids was achieved within 10 min. The linearity was achieved in the range of 0.30-1.0 mg (r=0.999 8) for rutin, 0.030-0.10 mg (r=0.999 8) for quercetin and 0.010-0.033 mg (r=0.999 5) for quercitrosid. The average recoveries were 100.95% (RSD 0.98%), 99.51% (RSD 1.54%) and 102.84% (RSD 3.53%) respectively. Conclusion: The method is simple, rapid and accurate, which can be able to detect rutin, quercetin and quercitroside simultaneously, and can be used for quality control of I. mairei.
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