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作 者:张雪莹[1] 张杨 张建逵[3] 韩荣春[3] 康廷国[3] 王冰[3]
机构地区:[1]沈阳佰佳安医疗健康用品有限公司,辽宁沈阳110031 [2]大连华立金港药业有限公司,辽宁大连116100 [3]辽宁中医药大学,辽宁大连116600
出 处:《中华中医药学刊》2011年第9期1987-1989,共3页Chinese Archives of Traditional Chinese Medicine
基 金:国家科技基础条件平台项目(2005DKA21000)
摘 要:目的:建立同时测定山楂叶中芦丁、金丝桃苷及槲皮素的分析方法。方法:采用多波长RP-HPLC法,色谱柱为Agilent Eclipse XDB-C18柱(4.6mm×150mm,5μm);流动相:乙腈(A)-0.025mol/L磷酸水(B),梯度洗脱依次为0~15min(18%A~18%A),15~30min(18%A~40%A);检测波长为363nm(0~18min),371nm(18~30min);流速:0.9mL/min;柱温:28℃。结果:芦丁、金丝桃苷及槲皮素的线性范围分别为0.3148~1.5740μg、0.4205~2.1024μg、0.0261~0.1305μg。平均加样回收率分别为100.29%、99.42%、98.86%,RSD分别为1.79%、1.46%、1.50%。结论:该方法简便、快速、准确,重现性好,可用于山楂叶中芦丁、金丝桃苷及槲皮素的同时测定。AIM: To establish a method for simultaneous determination of rutin, hyperoside, quercetin in Folium Cra- taegi. Methods: A multiple wavelength RP- HPLC method was developed. The analysis was performed on an Agilent E- clipse XDB - C18column (4.6mm 150mm, 5μm). A mixture of acetonitrile (A) - 0. 025mol/L phosphoric acid (B) with gradient elution as the mobile phase was adopted. The gradient elution program was 0 ~ 15min (18% A ~ 18% A), 15 ~ 30min ( 18% A ~ 40% A) ; The wavelength was monitored 363nm (0 ~ 18min), 371nm( 18 - 30min). The flow rate was 0.9 mL/min. The column temperature was 28 ℃. Results:The linear response ranges of rutin, hyperoside, quercetin were 0. 3148 - 1. 57401xg, 0. 4205 ~ 2. 1024μg, 0. 0261 - 0. 1305txg respectively. The average recoveries were 100.29%, 99.42%, 98.86% with RSD of 1.79%, 1.46%, 1.50% respectively. Conclusion: The method is simple and reproducible for determining rutin, hyperoside, quercetin in Folium Crataegi.
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