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Extraction and Purification of Flavonoids from Radix Puerariae

机译:葛根中黄酮类化合物的提取与纯化

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Purpose: To develop an efficient method for the purification of flavonoids from Radix puerariae Methods: Optimal extraction technology was obtained using orthogonal test. Through adsorption and desorption tests, 8 resins with different polarity, diameter, and surface area were studied. Finally, a novel macroporous resin, HPD200A, was applied in the work. Desorption tests were performed in a glass column packed with HPD200A resin, and several parameters of purification were studied. The content of puerarin and flavonoids in the samples were tested by a HPLC and a UV-Vis Spectrophotometer, respectively. Results: Optimum extraction technology was confirmed as follows: extraction time is 1.5 h; ratio of solvent to material 12; and repetition of extraction 3 times. Optimum purification technology was confirmed as follows: decoction is concentrated into 1.05 ~ 1.10 g/ml; 95 % ethanol is added to remove the impurities and the volume ratio is 1.5 : 1; the concentration of loading sample is 0.25 g/ml (based on the weight of the crude drug), the volume of loading sample is 2 BV (bed volume). The mobile phases of desorption are water (2BV) and 30 % ethanol (4BV) in succession. The contents of puerarin and flavonoids in the extract were improved greatly after the purification procedure, by up to 32 and 75 %, respectively. Conclusion: This efficient method has potential for purification and preparation of flavonoids in the future.
机译:目的:建立有效的葛根中黄酮类化合物的纯化方法。方法:采用正交试验获得最佳提取工艺。通过吸附和解吸测试,研究了8种极性,直径和表面积不同的树脂。最后,一种新的大孔树脂HPD200A被用于该工作。在装有HPD200A树脂的玻璃柱中进行解吸测试,并研究了几个纯化参数。样品中的葛根素和类黄酮含量分别通过HPLC和UV-Vis分光光度计进行测试。结果:确定最佳提取工艺如下:提取时间为1.5 h;提取时间为1.5 h。溶剂与材料12的比例;并重复提取3次。确定最佳纯化工艺如下:将汤浓缩至1.05〜1.10 g / ml;加入95%乙醇以除去杂质,体积比为1.5∶1。上样量为0.25 g / ml(基于原料药的重量),上样量为2 BV(床体积)。解吸的流动相依次是水(2BV)和30%乙醇(4BV)。纯化后,提取物中的葛根素和类黄酮含量大大提高,分别提高了32%和75%。结论:该高效方法在将来有可能纯化和制备类黄酮。

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