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Orthogonal test design for optimizing the extraction of total flavonoids from Flos pueraria

机译:正交试验设计优化葛根中总黄酮的提取

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The conditions for extraction of the total flavonoids from Flos pueraria was optimized and the purification and separation process were conducted to identify the main constituents of the total flavonoids as well. The solvent for extraction and its concentration, the solid-to-liquid ratio, extraction duration, temperature and ultrasonic frequency were investigated through a single-factor experiment. An orthogonal design (L9 (34) was constructed to achieve the best extraction conditions. The crude extract was then purified sequentially by petroleum ether, ethanol and chloroform, n-butyl alcohol, and eluted gradually with mixed mobile phase of methanol-chloroform solution in the silica gel column system. The ingredients were further separated by color reaction, ultraviolet spectrophotometry, high performance liquid chromatography, infrared and mass spectral analysis. The optimum extraction condition for the total flavonoids from F. pueraria was as follows: extraction? by 50% (v/v) methanol solution, the solid-to-liquid ratio at 1:30, extraction duration 2.0 h, the temperature of 70°C, ultrasound 3 times and 30 min each time. Five isoflavones were separated and identified as irisolidone, genistein, daidzein, kakkalide and puerarin, respectively. Under these optimal conditions, the yield of total flavonoids in the extracts was up to 17.5%, while the output rate previously reported is about 8% in general. Our study provided means for further development and utilization of the bioactive components from F. pueraria.
机译:优化了从葛根中提取总黄酮的条件,并进行了纯化和分离工艺以鉴定总黄酮的主要成分。通过单因素实验研究了萃取溶剂及其浓度,固液比,萃取时间,温度和超声频率。构建正交设计(L9(34))以达到最佳提取条件,然后将粗提取物依次用石油醚,乙醇和氯仿,正丁醇纯化,并用甲醇-氯仿溶液的混合流动相逐渐洗脱。通过颜色反应,紫外分光光度法,高效液相色谱,红外和质谱分析进一步分离成分,从葛根中提取总黄酮的最佳提取条件为:提取率50%。 (v / v)甲醇溶液,固液比为1:30,萃取时间为2.0 h,温度为70°C,超声3次,每次30 min,分离出5种异黄酮,鉴定为伊立替酮在最佳条件下,提取物中总黄酮的收率高达17.5%,而先前报道的产量为一般约8%。我们的研究为进一步开发和利用葛根生物活性成分提供了手段。

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