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Micro- and nano-encapsulation and controlled-release of phenolic compounds and other food ingredients.

机译:酚类化合物和其他食品成分的微囊和纳米囊化以及控释。

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摘要

The health promotive properties of phenolic compounds attracted a lot of attention in recent years because of their biological and pharmacological effects including antioxidative and cytoprotective functions. Green tea catechins and curcumin have been extensively studied and they both show strong anti-oxidant and anti-inflammatory properties, but low bioavailability is always a problem. Therefore, effective delivery systems could be a solution to enhance their oral bioavailability.In this study tea catechins were encapsulated in two W/O/W double emulsion systems, protein-polysaccharide complex coacervates and emulsifiers/polysaccharide stabilized double emulsion. Physicochemical characteristics were determined for both systems. The coacervate encapsulation achieved 90.5% encapsulation efficiency, and the other double emulsion reached 94.5% efficiency. Coacervate-encapsulated catechins were stable in artificial gastric juice, and could target-release catechins in small intestinal juice triggered by pH.Curcumin was dissolved in medium chain triglyceride (MCT) and further emulsified in water. Curcumin nano-emulsions had average particle sizes of 150.5nm and 148.4nm for 1% and 1.5% curcumin, respectively. The encapsulation efficiencies were 77.5% for 1% curcumin emulsion and 71.5% for 1.5% emulsion. Oral administration of nano-emulsified curcumin could inhibit TPA-induced edema on mouse ears by 100%, and significantly inhibited pro-inflammatory factors IL-1beta, IL-6, MMP-9, and cyclin D1 dose-responsively. The anti-inflammatory effects directly indicated enhanced bioavailability of curcumin.Protein-polysaccharide coacervation was further applied to enzyme encapsulation. alpha-Amylase can form coacervate with kappa-carrageenan under optimized conditions, and reach 99.3% encapsulation efficiency. Enzyme kinetics showed that encapsulation could strongly protect alpha-Amylase from acid denaturation, suggesting that the stoichiometric complexation of alpha-amylase did not alter the active binding sites of enzyme.In summary, low cost, convenient and highly efficient encapsulation methods using food grade natural biopolymers have been developed to encapsulate nutraceuticals or enzyme. The encapsulation systems have protective, target-releasing, and bioavailability enhancing functions.
机译:近年来,由于酚类化合物的生物学和药理作用(包括抗氧化和细胞保护功能),其促进健康的特性引起了很多关注。绿茶儿茶素和姜黄素已被广泛研究,它们均显示出强大的抗氧化和抗炎特性,但生物利用度低始终是一个问题。因此,有效的递送系统可能是提高其口服生物利用度的解决方案。在这项研究中,茶儿茶素被包裹在两种W / O / W双乳剂体系中,即蛋白质-多糖复合物凝聚层和乳化剂/多糖稳定的双乳剂。确定了两个系统的理化特性。凝聚层的包封率达到了90.5%,另一种双重乳液的效率达到了94.5%。凝聚包封的儿茶素在人造胃液中是稳定的,并且可以在pH触发的小肠汁中靶向释放儿茶素。姜黄素溶解在中链甘油三酸酯(MCT)中并在水中进一步乳化。姜黄素纳米乳剂的姜黄素含量分别为1%和1.5%,平均粒径分别为150.5nm和148.4nm。对于1%姜黄素乳液,包封效率为77.5%,对于1.5%乳液,包封效率为71.5%。口服纳米乳化姜黄素可以100%抑制TPA诱导的小鼠耳部水肿,并显着抑制促炎因子IL-1beta,IL-6,MMP-9和cyclin D1的剂量反应性。抗炎作用直接表明姜黄素具有更高的生物利用度。蛋白-多糖凝聚进一步应用于酶包囊。在最佳条件下,α-淀粉酶可与κ-角叉菜胶形成凝聚层,包封效率达到99.3%。酶动力学表明,包囊可以强烈保护α-淀粉酶免于酸变性,这表明α-淀粉酶的化学计量配合不会改变酶的活性结合位点。总之,使用食品级天然食品的低成本,方便,高效的包囊方法生物聚合物已经被开发来封装营养品或酶。封装系统具有保护,释放目标和提高生物利用度的功能。

著录项

  • 作者

    Jiang, Yan.;

  • 作者单位

    Rutgers The State University of New Jersey - New Brunswick.;

  • 授予单位 Rutgers The State University of New Jersey - New Brunswick.;
  • 学科 Agriculture Food Science and Technology.Health Sciences Nutrition.
  • 学位 Ph.D.
  • 年度 2009
  • 页码 146 p.
  • 总页数 146
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-17 11:38:11

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