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机构地区:[1]桂林医学院,广西桂林541004 [2]桂林医学院附属医院,广西桂林541004
出 处:《中国实验方剂学杂志》2014年第22期29-32,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:广西自然科学基金项目(2012GXNSFAA053148)
摘 要:目的:优选D101型大孔树脂纯化九龙藤总黄酮的工艺条件,为该成分的工业制剂开发提供参考。方法:以总黄酮纯度及回收率为评价指标,在单因素试验基础上,采用正交试验考察上样液质量浓度、洗脱剂浓度、洗脱速度及上样液p H对九龙藤总黄酮大孔树脂纯化工艺的影响。采用UV测定黄芩苷含量,检测波长278.5 nm。结果:最佳纯化工艺为上样液质量浓度15.5 g·L^-1,上样液pH 2-3,最大上样量16.85 mg·g^-1,上样速度0.125 BV·h^-1,径高比1∶6,加60%乙醇4 BV以1 BV·h^-1洗脱。总黄酮纯度48.95%,回收率96.08%。结论:优选的纯化工艺稳定可行,有效提高了九龙藤总黄酮纯度及回收率,适用于九龙藤总黄酮的纯化。Objective: To optimize purification process of total flavonoids from Bauhinia championii by D101 macroporous resin and provide a reference for preparations development of these components. Method: With purity and recovery of total flavonoids as indexes, based on single factor tests, orthogonal design was used to optimize purification process by taking eluent concentration,elution rate,p H and concentration of sample solution as factors. UV was employed to determine the content of baicalin with detection wavelength at 278. 5 nm. Result:Optimal purification process was as following: the concentration of sample solution 15. 5 g·L^-1,p H of sample solution 2-3,the maximum sample volume of 16. 85 mg·g^- 1,sampling rate of 0. 125 BV·h^-1,diameter and height ratio of 1∶ 6,eluted by 4 BV of 60% ethanol with elution speed of 1 BV·h^-1. Under this process,purity and recovery were 48. 95% and 96. 08%, respectively. Conclusion: This optimized purification process is stable,feasible and suitable for purifying total flavonoids from B. championii,which can effectively improve its purity and recovery.
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