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中国精品科技期刊2020
高林晓,马文升,石慧丽,等. Box-Behnken模型优化水麻叶总黄酮提取工艺及抗氧化活性分析[J]. 食品工业科技,2021,42(12):184−190. doi: 10.13386/j.issn1002-0306.2020080230.
引用本文: 高林晓,马文升,石慧丽,等. Box-Behnken模型优化水麻叶总黄酮提取工艺及抗氧化活性分析[J]. 食品工业科技,2021,42(12):184−190. doi: 10.13386/j.issn1002-0306.2020080230.
GAO Linxiao, MA Wensheng, SHI Huili, et al. Optimization of the Ultrasound Extraction Technology and Antioxidant Activity Analysis of the Total Flavonoids from Debregeasia orientalis Leaves by Box-Behnken Method[J]. Science and Technology of Food Industry, 2021, 42(12): 184−190. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2020080230.
Citation: GAO Linxiao, MA Wensheng, SHI Huili, et al. Optimization of the Ultrasound Extraction Technology and Antioxidant Activity Analysis of the Total Flavonoids from Debregeasia orientalis Leaves by Box-Behnken Method[J]. Science and Technology of Food Industry, 2021, 42(12): 184−190. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2020080230.

Box-Behnken模型优化水麻叶总黄酮提取工艺及抗氧化活性分析

Optimization of the Ultrasound Extraction Technology and Antioxidant Activity Analysis of the Total Flavonoids from Debregeasia orientalis Leaves by Box-Behnken Method

  • 摘要: 本文以水麻叶为原料,通过单因素实验设计Box-Behnken模型,优选出提取水麻叶总黄酮最佳工艺条件,并评价了其体外抗氧化活性。结果表明:乙醇浓度、液料比、超声时间、超声温度分别为35%、42 mL/g、47 min、70 ℃时,与Box-Behnken模型的预测值相符。验证试验得到水麻叶总黄酮得率为3.15%±1.82%。在此条件下,提取液的总抗氧化能力为1.969 mmol/L(FeSO4当量值),DPPH自由基清除能力IC50为0.075 mg/mL。表明水麻叶提取液中的总黄酮可展现出良好的抗氧化活性,为进一步研究开发水麻野生资源提供一定的理论数据支撑。

     

    Abstract: Using Debregeasia orientalis leaves as raw materials, the Box-Behnken model was designed by single factor experiments and the optimal technological conditions for extracting total flavonoids from Debregeasia orientalis leaves were optimized, and the antioxidant activity in vitro was evaluated. The results showed that the ethanol concentration, liquid-material ratio, ultrasonic time and ultrasonic temperature were 35%, 42 mL/g, 47 min and 70 ℃, respectively, which were consistent with the predicted values of Box-Behnken model. The average extraction rate of total flavonoids from Debregeasia orientalis leaves was 3.15%±1.82%. Under these conditions, the total antioxidant capacity of extract was equivalent to 1.969 mmol/L (FeSO4 equivalent value), and the IC50 of DPPH free radical scavenging rate was 0.075 mg/mL, which indicated that the total flavonoids of the extract from Debregeasia orientalis leaves could exhibit good antioxidant activity, and provide certain theoretical data support for further research and development of wild resources of Debregeasia orientalis.

     

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