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中国精品科技期刊2020
张子豪,徐硕,逄格雨,等. 玉米醇溶蛋白纳米颗粒的体外消化特性[J]. 食品工业科技,2023,44(13):1−8. doi: 10.13386/j.issn1002-0306.2022110187.
引用本文: 张子豪,徐硕,逄格雨,等. 玉米醇溶蛋白纳米颗粒的体外消化特性[J]. 食品工业科技,2023,44(13):1−8. doi: 10.13386/j.issn1002-0306.2022110187.
ZHANG Zihao, XU Shuo, PANG Geyu, et al. In Vitro Digestive Properties of Zein Nanoparticles[J]. Science and Technology of Food Industry, 2023, 44(13): 1−8. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022110187.
Citation: ZHANG Zihao, XU Shuo, PANG Geyu, et al. In Vitro Digestive Properties of Zein Nanoparticles[J]. Science and Technology of Food Industry, 2023, 44(13): 1−8. (in Chinese with English abstract). doi: 10.13386/j.issn1002-0306.2022110187.

玉米醇溶蛋白纳米颗粒的体外消化特性

In Vitro Digestive Properties of Zein Nanoparticles

  • 摘要: 为了研究基于天然生物大分子的纳米递送体系在消化过程中物理化学性质的变化,本研究以姜黄素(Curcumin)为芯材,玉米醇溶蛋白(Zein)为壁材,通过反溶剂沉淀法制备了包埋姜黄素的玉米醇溶蛋白纳米颗粒(CZNPs),通过光谱学方法和电子显微镜对CZNPs的物化性质进行了表征,并在体外模拟消化模型中对CZNPs的消化特性进行了研究。结果表明,当姜黄素与Zein的质量比为1:40时,姜黄素的包埋率最高,为99%±1%,制得的CZNPs为球形纳米颗粒,平均粒径为118.6±0.7 nm、Zeta电位为19.9±3.79 mV,且颗粒之间出现轻微粘连。在体外模拟胃消化过程中,随着消化时间的延长,CZNPs出现明显聚集,其平均粒径增至8000 nm;且部分Zein发生降解,生成小分子量的氨基酸,同时缓慢释放出姜黄素。在后续的模拟肠消化过程中,CZNPs的聚集程度随着消化时间的延长而明显减弱,但Zein没有继续降解,姜黄素的释放也没有明显增大。因此,玉米醇溶蛋白纳米颗粒是一种比较有效的口服递送体系,可能应用于功能性食品和口服药物的开发中。

     

    Abstract: To investigate changes in the physicochemical properties of nano delivery systems that were fabricated by native biomacromolecules during digestion, curcumin and zein were separately used as the core and shell materials in this study, and curcumin-loaded zein nanoparticles (CZNPs) were prepared by the way of inverse solvent precipitation. Firstly, the physicochemical properties of CZNPs were characterized by various spectroscopy and electron microscopy methods. Then, the digestive properties of CZNPs in an in vitro simulated digestion model were investigated. Results showed that the encapsulation efficiency of Cur (99%±1%) was the largest when the mass ratio of Cur and zein was 1:40. Moreover, the obtained CZNPs were spherical nanoparticles with an average particle size of 118.6±0.7 nm and zeta potential of 19.9±3.79 mV. Slight adhesion between CZNPs was also noticed. During in vitro simulated gastric digestion, with the increase of digestive time, significant aggregation occurred and the average particle size of CZNPs increased to 8000 nm. Meanwhile, part of zein degraded into amino acids and Cur was released slightly. During the subsequent simulated intestinal digestion, the aggregation of CZNPs reduced with time. However, zein kept stable without continue degradation and the release of Cur didn’t change significantly. Therefore, zein nanoparticles may be an effective oral delivery system with possible applications in the development of functional foods and orally administered drugs.

     

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