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中国精品科技期刊2020
晏武,黄冬成,戈丹,等. 枳椇果梗皂苷提取工艺优化及抗氧化活性分析J. 食品工业科技,2026,47(18):1−10. doi: 10.13386/j.issn1002-0306.2025100130.
引用本文: 晏武,黄冬成,戈丹,等. 枳椇果梗皂苷提取工艺优化及抗氧化活性分析J. 食品工业科技,2026,47(18):1−10. doi: 10.13386/j.issn1002-0306.2025100130.
YAN Wu, HUANG Dongcheng, GE Dan, et al. Extraction Optimization and Antioxidant Activity of Saponins from Hovenia dulcis PedicelsJ. Science and Technology of Food Industry, 2026, 47(18): 1−10. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025100130.
Citation: YAN Wu, HUANG Dongcheng, GE Dan, et al. Extraction Optimization and Antioxidant Activity of Saponins from Hovenia dulcis PedicelsJ. Science and Technology of Food Industry, 2026, 47(18): 1−10. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2025100130.

枳椇果梗皂苷提取工艺优化及抗氧化活性分析

Extraction Optimization and Antioxidant Activity of Saponins from Hovenia dulcis Pedicels

  • 摘要: 为提高枳椇果梗的资源化利用率,本研究旨在优化其皂苷提取工艺并评价其抗氧化活性。采用匀浆辅助超声法提取HDPS,在单因素实验基础上,利用响应面法优化提取工艺参数,并采用D101大孔树脂对粗提物进行纯化。通过傅里叶变换红外光谱(FT-IR)和超高效液相色谱-串联质谱(UPLC-MS/MS)对纯化产物进行结构表征与成分鉴定,最后通过体外抗氧化模型验证HDPS对DPPH·、ABTS+·、羟自由基清除率及铁还原力测定。结果表明,最佳提取工艺条件为:乙醇浓度49%、液料比30:1 mL/g、匀浆超声时间21 min、超声功率400 W、匀浆功率500 W,在此条件下HDPS得率为4.41%±0.13%。经D101大孔树脂纯化后,HDPS纯度由34.37%显著提高至67.12%。UPLC-MS/MS分析表明HDPS主要含有棘孢苷B、酸枣仁皂苷、拐枣皂苷B等皂苷类成分。体外抗氧化实验显示,HDPS对DPPH·、ABTS+·和羟自由基具有显著的清除能力,其IC50值分别为165.3、56.2和168.7 μg/mL,同时具有一定的铁还原力。本研究为枳椇果梗的综合开发利用及其在功能性食品领域的应用提供了理论依据和技术支持。

     

    Abstract: In order to improve the resource utilization rate of Hovenia dulcis pedicels (HDPS), the purpose of this study was to optimize the extraction process of saponins and evaluate their antioxidant activity. HDPS was extracted by the homogenization-assisted ultrasonic extraction. On the basis of a single-factor experiment, the extraction process parameters were optimized by the response surface methodology, and the crude extract was purified by D101 macroporous resin. The structure and composition of the purified product were characterized by Fourier transform infrared spectroscopy (FT-IR) and ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). Finally, the DPPH·, ABTS+·, ·OH radicals, and the ferric reducing power of HDPS were verified by an in vitro antioxidant model. The results showed that the optimum extraction conditions were as follows: ethanol concentration 49%, liquid-to-solid ratio 30:1 mL/g, homogenization ultrasonic time 21 min, ultrasonic power 400 W, homogenization power 500 W. Under these conditions, the yield of HDPS was 4.41%±0.13%. After purification by D101 macroporous resin, the purity of HDPS was significantly increased from 34.37% to 67.12%. UPLC-MS/MS analysis showed that HDPS mainly contained saponins such as echinacoside B, jujuboside B, and so on. In vitro antioxidant experiments showed that HDPS had significant scavenging ability to DPPH·, ABTS+·, and ·OH radicals, and its IC50 values were 165.3, 56.2, and 168.7 μg/mL, respectively, and had a certain iron reducing power. This study provides a theoretical basis and technical support for the comprehensive development and utilization of Hovenia dulcis fruit stem and its application in the field of functional food.

     

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