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在模拟小肠的细胞培养模型存在的情况下,牛奶消化过程中的纳米结构生成。

Nanostructure generation during milk digestion in presence of a cell culture model simulating the small intestine.

机构信息

Laboratory for Particles-Biology Interactions, Empa, Swiss Federal Laboratories for Materials Science and Technology, Lerchenfeldstrasse 5, 9014 St. Gallen, Switzerland; Department of Health Sciences and Technology, ETH Zürich, Zürich, Switzerland.

Laboratory for Biointerfaces, Empa, Swiss Federal Laboratories for Materials Science and Technology, Lerchenfeldstrasse 5, 9014 St. Gallen, Switzerland.

出版信息

J Colloid Interface Sci. 2020 Aug 15;574:430-440. doi: 10.1016/j.jcis.2020.04.059. Epub 2020 Apr 18.

Abstract

HYPOTHESIS

The development of advanced oral delivery systems for bioactive compounds requires the fundamental understanding of the digestion process within the gastrointestinal tract. Towards this goal, dynamic invitro digestion models, capable of characterising the molecular as well as colloidal aspects of food, together with their biological interactions with relevant invitro cell culture models, are essential.

EXPERIMENTS

In this study, we demonstrate a novel digestion model that combines flow-through time resolved small angle X-ray scattering (SAXS) with an invitro Caco-2/HT-29 cell co-culture model that also contained a mucus layer. This set-up allows the dynamic insitu characterisation of colloidal structures and their transport across a viable intestinal cell layer during simulated digestion.

FINDINGS

An integrated online SAXS - invitro cell co-culture model was developed and applied to study the digestion of nature's own emulsion, milk. The impact of the invitro cell culture on the digestion-triggered formation and evolution of highly ordered nanostructures in milk is demonstrated. Reported is also the crucial role of the mucus layer on top of the cell layer, protecting the cells from degradation by digestive juice components such as lipase. The novel model can open unique possibilities for the dynamic investigation of colloidal structure formation during lipid digestion and their effect on the uptake of bioactive molecules by the cells.

摘要

假设

为了开发用于生物活性化合物的先进口服递药系统,需要从根本上了解胃肠道内的消化过程。为此,能够对食物的分子和胶体特性进行特征描述的动态体外消化模型,以及它们与相关的体外细胞培养模型的生物相互作用,是至关重要的。

实验

在这项研究中,我们展示了一种新的消化模型,它结合了流动式时间分辨小角 X 射线散射(SAXS)和体外 Caco-2/HT-29 细胞共培养模型,其中还包含一层黏液层。这种设置允许在模拟消化过程中对胶体结构及其在有活力的肠细胞层中的传输进行原位动态特性描述。

发现

开发并应用了一种集成的在线 SAXS-体外细胞共培养模型,以研究天然乳液(牛奶)的消化。证明了体外细胞培养对消化触发的牛奶中高度有序纳米结构的形成和演变的影响。还报告了细胞层顶部黏液层的关键作用,它可以防止细胞被消化液成分(如脂肪酶)降解。这种新模型可以为脂质消化过程中胶体结构形成的动态研究及其对细胞吸收生物活性分子的影响提供独特的可能性。

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