期刊文献+

大孔树脂纯化菊米总黄酮的工艺研究 被引量:1

Purification technology of total flavonoids from buds of Chrysanthemum indicum with macroporous resin
原文传递
导出
摘要 目的探究一种有效分离纯化菊米黄酮的大孔树脂并对纯化工艺条件进行优化。方法以树脂的饱和吸附容量、吸附速率和解吸附率为参考指标,从10种不同的大孔吸附树脂中筛选出综合性能较佳的树脂,并进一步考察此树脂纯化菊米总黄酮的影响因素和分离纯化效果。结果 HPD-100树脂的综合性能较好,饱和吸附容量达到60.2 mg/g(以湿重计),且吸附迅速,解吸附完全。较理想的吸附工艺:在树脂径高比为1∶10的条件下,质量浓度为4.3 mg/mL供试液以15 mL/min上柱时,最佳上样量为5倍柱床体积(BV),静态吸附时间为2 h;较理想的洗脱工艺:先用6 BV的纯水洗杂质,再以60%的乙醇为洗脱剂,洗脱体积流量为8 mL/min时,用量为3 BV,所得菊米总黄酮质量分数为(81.6±0.9)%。结论 HPD-100是一种分离纯化菊米黄酮较佳的树脂,其工艺简单,具有较好的工业化生产前景。 Objective To screen a macroporous resin for effective separating and purifying the total flavonoids from the buds of Chrysanthemum indicum(TFBCI) and to further optimize the process conditions.Methods Through critical evaluating the absorption and desorption properties of macroporous resins including the absorption capacity,absorption velocity,and desorption rate,a preferable resin was selected from 10 kinds of macroporous resins,and the influence factors and purification effect on TFBCI were investigated further.Results HPD-100 resin had outstanding comprehensive performance,maximum static adsorption capacity was60.2 mg/g(wet resin),and the adsorption was rapid and desorption complete.The optimum adsorption process was:under the condition of the resin's diameter height ratio of 1:10,the sample solution concentration 4.3mg/mL and flow rate 7mL/min,the best processing volume was 5 BV,and static adsorption time was 2h;The optimum elution process was:wash the impurities with 6 BV of pure water,elute product with 60% ethanol at the speed of 8 mL/min.The purity of the final product reached to(81.6±0.9)%.Conclusion HPD-100 is an ideal resin for separating and purifying the TFBCI,and its process is simple and has preferable industrialization prospect.
出处 《药物评价研究》 CAS 2013年第6期455-459,共5页 Drug Evaluation Research
基金 国家自然科学基金资助项目(21076191 21006097 21276237)
关键词 菊米 总黄酮 大孔树脂 吸附 纯化 buds of Chrysanthemum indicum L. total flavonoids macroporous resins adsorption purification
  • 相关文献

参考文献16

二级参考文献78

共引文献170

同被引文献12

引证文献1

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部