中药蒲公英花中总黄酮的分离纯化研究  

Separation and purification of total flavonoids from taraxacum mongolicum inflorescences

作　　者：卫建琮[1] 李华峰[2] 乔华[1] 弓辉[1] 孙体健[1] 

机构地区：[1]山西医科大学化学教研室,太原030001 [2]山西医学科学院 山西大医院药剂科

出　　处：《中国药物与临床》2014年第1期19-21,共3页Chinese Remedies & Clinics

基　　金：山西省科技攻关项目(20090311057-1)

摘　　要：目的 从中药蒲公英花中分离纯化总黄酮.方法 用超声波助提法得到蒲公英花黄酮粗提液,采用D-101 大孔吸附树脂对其进行纯化,并研究影响动态吸附与解吸的各种因素.结果 最佳分离纯化条件为：在D-101 树脂柱中,上样液浓度为1.238 mg/ml,pH 值为3,上样量为2 树脂床体积倍数（BV）,室温下以流速2.0BV/h 吸附饱和,用4 BV 的50%～70% 乙醇以2 BV/h 的流速洗脱,在此条件下,测得黄酮纯度为92.56%,吸附率为80.65%,解吸率为53.44%,回收率为42.8%.结论 在所确定的条件下,D-101 大孔吸附树脂分离纯化蒲公英花总黄酮效果良好,为蒲公英花总黄酮的开发利用提供了新途径.Objective To separate and purify the total flavonoids from Taraxaeum mongolicum infloreseences （TMI）. Methods The crude flavonoid extracts of TMI was prepared by ultrasonic extraction and purified with D-101 resin, which entailed the analysis on various factors contributing to dynamic absorption and desorption. Results The optimal technical conditions for purification was to supplement the maeroporous D-101 resins with 2 BV of crude flavonoid samples （pH： 3.0） at a velocity of 1.238 mg/ml at room temperature till saturation （2.0 BV/h）, followed by an elution with 4 BV 50%-70% ethanol at the rate of 2.0 BV/h. This gave a purity of 92.56%, an adsorption rate of 80.65%, a desorption rate of 53.44% and a recovery rate of 42.8%. Conclusion The D-101 macroporous adsorption resin confers a satisfactory capacity for purifying the total flavonoids from TMI under an optimal condition, which of-fers a new approach for developing and utilizing the total flavonoids.

关 键 词：蒲公英 黄酮 分离和提纯 

分 类 号：R284[医药卫生—中药学]