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机构地区:[1]西南大学化学化工学院发光与实时分析教育部重点实验室,重庆400715
出 处:《中国中医药信息杂志》2013年第12期59-61,共3页Chinese Journal of Information on Traditional Chinese Medicine
基 金:国家自然科学基金(21277110)
摘 要:目的以离子液体1-丁基-3-甲基咪唑溴化盐([BMIM]Br)为萃取剂超声辅助萃取,高效液相色谱法同时分离测定芦荟中的芦荟苷和芦荟大黄素。方法采用PhenomenexC18色谱柱(250mm×4.6mm,5μm);流动相:甲醇-0.3%冰醋酸水溶液(65:35);流速:0.80mL/min;紫外检测波长:360nm;柱温:35℃。结果芦荟苷和芦荟大黄素分别在0.000336-1.68lag(r=0.99996)、0.000608-3.04μg(r=0.99976)范围内线性关系良好,检出限分别为0.0506、0.262ng/mL,平均加样回收率分别为95.99%、95.80%。结论本法操作简单快速、定量准确、灵敏度高、成本低,且对环境友好,是检测及分离芦荟中蒽醌类化合物的有效方法。Objective To isolate and determine Aloin and Aloeemodin in Barbodos Aloe by ionic liquid-based ultrasonic-assisted extraction coupled with high performance liquid chromatography, with 1-butyl-3-methylimidazolium chloride ([BMIM]Br) solution as the extraction solvent. Methods The separation was performed on Phenomenex C18 column (250 mm×4.6 mm, 5 μm) with detection wavelength of 360 nm. The mobile phase was consisted of methanol-0.3% acetic acid solution (65 : 35) with the flow rate of 0.80 mL/min, and the column temperature at 35 ℃. Results The calibration curves for Aloin and Aloeemodin were liner within 0.000 336-1.68μg (r=0.999 96) and 0.000 608-3.04 μg (r= 0.999 76), respectively. The limit of detection (LOD) was 0.05 06 ng/mL and 0.262 ng/mL, respectively. The average recovery was 95.99% and 95.80%, respectively. Conclusion The method is simple, rapid, accurate, sensitive, low cost and environment-friendly, thus it provides an effective means for assaying anthraquinones in Barbodos Aloe.
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