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中国精品科技期刊2020

硒蛋白微胶囊的制备、结构表征及体外消化特性研究

徐威, 张碟, 蔡杰, 程水源, 丁文平, 祝振洲

徐威, 张碟, 蔡杰, 程水源, 丁文平, 祝振洲. 硒蛋白微胶囊的制备、结构表征及体外消化特性研究[J]. 食品工业科技, 2020, 41(14): 29-35. DOI: 10.13386/j.issn1002-0306.2020.14.005
引用本文: 徐威, 张碟, 蔡杰, 程水源, 丁文平, 祝振洲. 硒蛋白微胶囊的制备、结构表征及体外消化特性研究[J]. 食品工业科技, 2020, 41(14): 29-35. DOI: 10.13386/j.issn1002-0306.2020.14.005
XU Wei, ZHANG Die, CAI Jie, CHENG Shui-yuan, DING Wen-ping, ZHU Zhen-zhou. Preparation, Structural Characterization, and in Vitro Digestibility of Selenoprotein Microcapsules[J]. Science and Technology of Food Industry, 2020, 41(14): 29-35. DOI: 10.13386/j.issn1002-0306.2020.14.005
Citation: XU Wei, ZHANG Die, CAI Jie, CHENG Shui-yuan, DING Wen-ping, ZHU Zhen-zhou. Preparation, Structural Characterization, and in Vitro Digestibility of Selenoprotein Microcapsules[J]. Science and Technology of Food Industry, 2020, 41(14): 29-35. DOI: 10.13386/j.issn1002-0306.2020.14.005

硒蛋白微胶囊的制备、结构表征及体外消化特性研究

基金项目: 

武汉轻工大学引进(培养)人才科研启动项目(2016RZ22)

湖北省技术创新专项(重大项目)(2019ABA113)

中国科协"青年人才托举工程"项目(2018QNRC001)

农业农村富硒产品开发与质量控制重点实验室/富硒食品开发国家地方联合工程实验室开放课题资助项目(Se-2019A01)

湖北省"楚天学者计划"人才项目

恩施州公共检验检测中心标准化研究项目和恩施市科技支撑项目。

恩施州科技计划项目(D20170041,I20180002,D20190003)

武汉轻工大学杰出青年科学基金项目(2018J01)

详细信息
    作者简介:

    徐威(1996-),男,硕士研究生,研究方向:农产品加工,E-mail:xwismvp@163.com。

    通讯作者:

    蔡杰(1987-),男,博士,副教授,研究方向:碳水化合物结构与功能特性研究及富硒农产品精深加工与高效利用,E-mail:caijievip@hotmail.com

    程水源(1965-),男,博士,教授,研究方向:精加工富硒产品标准化和硒与大健康的应用,E-mail:s_y_cheng@sina.com。

  • 中图分类号: TS201.2

Preparation, Structural Characterization, and in Vitro Digestibility of Selenoprotein Microcapsules

  • 摘要: 为了提高植物硒蛋白的生物利用度,拓展其在富硒食品开发中的应用,本研究以海藻酸钠为壁材,CaCl2溶液为固化液,采用锐孔凝固浴法微囊化硒蛋白,并以硒蛋白包埋率为响应值,通过响应面试验优化硒蛋白微胶囊的制备工艺。进一步通过扫描电子显微镜(SEM)、傅里叶变换红外光谱仪(FTIR)、热重分析仪(TGA)以及体外模拟消化试验对硒蛋白微胶囊的微观形态、分子结构、热稳定性及胃肠道消化特性进行了研究。最佳工艺条件为海藻酸钠浓度1.6%(w/v)、CaCl2浓度2%(w/v)以及包埋操作温度49 ℃,此时硒蛋白包埋率可达87.4%。表征测试证实了海藻酸钠组成的微胶囊结构能高效且紧实包裹硒蛋白,硒蛋白微胶囊平均粒径为(848.1±60.2) μm,且热稳定性能得到了改善。在模拟胃液体系中,硒蛋白的释放量仅为8.9%,而模拟肠液体系中13 h后累计释放达88.2%,表明微胶囊化能有效保护硒蛋白、提高稳定性和缓释性。本研究相关结论有望为硒蛋白的高值化利用以及富硒食品的开发提供新方法。
    Abstract: This study aimed to improve the bioavailability of plant-derived selenoprotein and extend its application for the development of Se-enriched food. Microencapsulated selenoprotein was prepared by piercing-solidifying method with sodium alginate as wall material and CaCl2 aqueous solution as curing solution, respectively. The technology process was further optimized by response surface methodology using the embedding rate of selenoprotein as response value. The micro morphology, molecular structure, thermal stability, and in vitro digestibility of products was characterized by scanning electron microscope (SEM), Fourier transform infrared spectrum (FTIR), thermogravimetric analysis (TGA), and simulating digestion experiments, respectively. The results showed that the optimal conditions were sodium alginate concentration 1.6% (w/v), CaCl2 concentration 2% (w/v), and embedding operation temperature 49℃. The selenoprotein embedding rate could reach 87.4%. The related characterization further confirmed that selenoprotein with average diameter of (848.1±60.2) μm was effectively and tightly wrapped, and its thermal stability was also improved. The in vitro digestion trial indicated that the release rate of the selenoprotein in the gastric juice system was only 8.9%, while the cumulative release rate in the intestinal system after 13 hours was 88.2% because microcapsules could effectively protect selenoproteins and improve its stability and slow release capacity. Related research of this work may provide a new route for the high-value utilization of selenoprotein and the development of Se-enriched food.
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出版历程
  • 收稿日期:  2019-09-22
  • 网络出版日期:  2020-11-12
  • 刊出日期:  2020-07-14

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