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中国精品科技期刊2020
王清,贾蕾,刘涛,等. 右旋糖酐纳米硒的制备表征及其稳定性和体外抗氧化活性分析J. 食品工业科技,2025,46(18):74−81. doi: 10.13386/j.issn1002-0306.2024090224.
引用本文: 王清,贾蕾,刘涛,等. 右旋糖酐纳米硒的制备表征及其稳定性和体外抗氧化活性分析J. 食品工业科技,2025,46(18):74−81. doi: 10.13386/j.issn1002-0306.2024090224.
WANG Qing, JIA Lei, LIU Tao, et al. Preparation and Characterization of DEX-SeNPs and Analysis of Its Stability and Antioxidant Activity in VitroJ. Science and Technology of Food Industry, 2025, 46(18): 74−81. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2024090224.
Citation: WANG Qing, JIA Lei, LIU Tao, et al. Preparation and Characterization of DEX-SeNPs and Analysis of Its Stability and Antioxidant Activity in VitroJ. Science and Technology of Food Industry, 2025, 46(18): 74−81. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2024090224.

右旋糖酐纳米硒的制备表征及其稳定性和体外抗氧化活性分析

Preparation and Characterization of DEX-SeNPs and Analysis of Its Stability and Antioxidant Activity in Vitro

  • 摘要: 目的:优化右旋糖酐纳米硒(Dextran-Selenium nanoparticles,DEX-SeNPs)的制备工艺,检测其形态特征及评价体外抗氧化能力,并探究右旋糖酐(Dextran,DEX)稳定纳米硒(Selenium nanoparticles,SeNPs)的机制。方法:以DXE为分散剂和稳定剂,通过化学还原法制备DEX-SeNPs,通过单因素实验对其制备工艺进行探究,采用粒度仪、紫外光谱、红外光谱、X射线衍射等对其结构进行表征,之后进一步讨论其稳定性机制,探究其羟基自由基清除能力。结果:DEX-SeNPs制备的最优条件是抗坏血酸与亚硒酸钠摩尔比4:1,反应温度40 ℃,反应时间1 h。确定了DEX-SeNPs为无定型态零价硒,呈均匀规则的球形,平均尺寸114 nm,多分散性指数为0.038,在4 ℃存储条件下可保持稳定的胶体溶液状态30 d,并具有较好的羟基自由基清除能力。DEX稳定SeNPs的可能机制为:SeNPs表面的硒原子与DEX的羟基基团结合,形成Se···HO氢键以防止SeNPs聚集。结论:DEX-SeNPs的制备为多糖基SeNPs补硒制剂的研发与其生物活性应用研究提供了理论数据支撑。

     

    Abstract: Objective: To optimize the preparation process of dextran nano-selenium (DEX-SeNPs), detect its morphological characteristics, and evaluate its antioxidant capacity in vitro, while exploring the mechanism of dextran (DEX) stabilizing nano-selenium (SeNPs). Methods: DEX-SeNPs were prepared using DXE as a dispersant and stabilizer through a chemical reduction method. The preparation process was investigated using single-factor tests. The structure was characterized using particle size analyzers, UV spectroscopy, IR spectroscopy, and X-ray photoelectron spectroscopy. The stability mechanism was further discussed, and the hydroxyl radical scavenging ability was explored. Results: The optimal conditions for preparing DEX-SeNPs were a molar ratio of ascorbic acid to sodium selenite of 4:1, a reaction temperature of 40 ℃, and a reaction time of 1 hour. DEX-SeNPs were identified as amorphous zero-valent selenium, uniformly spherical in shape, with an average size of 114 nm and a polydispersity index of 0.038. They maintained a stable colloidal solution state at 4 ℃ for 30 days and exhibited good hydroxyl radical scavenging ability. The possible mechanism for DEX stabilizing SeNPs was the combination of selenium atoms on the surface of SeNPs with hydroxyl groups of DEX, forming Se···HO hydrogen bonds to prevent aggregation of SeNPs. Conclusion: The preparation of DEX-SeNPs provided theoretical data support for the development of polysaccharide-based SeNPs selenium supplements and research on their biological activity applications.

     

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