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黏液与包载生物活性物的脂质体相互作用:Caco-2 细胞和 Caco-2/HT29-MTX 共培养物上的界面张力测定法和细胞摄取。

Mucus interactions with liposomes encapsulating bioactives: Interfacial tensiometry and cellular uptake on Caco-2 and cocultures of Caco-2/HT29-MTX.

机构信息

University of Guelph, Department of Food Science, Stone Rd 50, N1G 2W1 Guelph, ON, Canada.

University of Guelph, Department of Food Science, Stone Rd 50, N1G 2W1 Guelph, ON, Canada.

出版信息

Food Res Int. 2017 Feb;92:128-137. doi: 10.1016/j.foodres.2016.12.010. Epub 2016 Dec 29.

Abstract

Structuring of delivery matrices in foods aquires careful designing for optimal delivery and subsiquent absorption of the beneficial compounds in the gut. There has been quite improvement in mimicking digestion and absorption in vitro but as of yet little is understood on mucus interference in nutrient absorption Therefore in this study interactions of human intestinal mucus with milk and soy phospholipids liposomes carring hydrophilic (epigallocatechin-3-gallate) or hydrophobic (β-carotene) bioactive molecules were investigated. Liposomes of about 100nm were obtained using microfluidization and their behaviour with the human intestinal mucus were evaluated using drop shape tensiometry. The chemistry of the liposomes (milk or soy) and the encapsulated bioactive structure can affect the viscoelastic behaviour of the complex itself. Empty or loaded liposomes were differently interacting with the mucus at the interface. Mucus-liposomes interactions were also studied using cell cultures, Caco-2 (without mucus) and cocultures Caco-2/HT29-MTX (mucus producing). The interaction of mucus layer with liposomes was at some extent aligned with rheological studies. This work demonstrated that delivery systems may interact with the mucosal surface of intestinal cells, and in vitro approaches allow for screening of such interactions. These highlights could help us in carefully designing the delivery systems and moreover choosing the right carrier and/or bioactive that does not jeopardize the optimal delivery of the bioactive structure.

摘要

在食品中构建输送矩阵需要精心设计,以实现有益化合物在肠道中的最佳输送和随后的吸收。在模拟消化和吸收方面已经取得了相当大的进展,但对于粘液对营养吸收的干扰知之甚少。因此,在这项研究中,研究了人肠道粘液与携带亲水性(表没食子儿茶素-3-没食子酸酯)或疏水性(β-胡萝卜素)生物活性分子的牛奶和大豆磷脂脂质体的相互作用。使用微流化法获得了约 100nm 的脂质体,并使用滴形张力计评估了它们与人肠道粘液的相互作用。脂质体的化学性质(牛奶或大豆)和包封的生物活性结构可以影响复合物本身的粘弹性行为。空脂质体或负载脂质体在界面上与粘液以不同的方式相互作用。还使用细胞培养物(无粘液的 Caco-2 和产生粘液的 Caco-2/HT29-MTX 共培养物)研究了粘液-脂质体相互作用。粘液层与脂质体的相互作用在某种程度上与流变学研究一致。这项工作表明,输送系统可能与肠细胞的粘膜表面相互作用,并且体外方法允许筛选这种相互作用。这些要点可以帮助我们精心设计输送系统,并且可以选择不会危及生物活性结构最佳输送的正确载体和/或生物活性物质。

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