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基于果胶的分子结构和界面特性研究果胶基乳液在上消化道中的不稳定性。

The instability of pectin-based emulsions in the upper digestive tract investigated based on the molecular structure and interfacial properties of pectin.

机构信息

Institute of Food Science and Technology, Chinese Academy of Agricultural Sciences, Beijing 100193, China.

Institute of Food Science and Technology, Chinese Academy of Agricultural Sciences, Beijing 100193, China; College of Food Science and Engineering, Qingdao Agricultural University, Qingdao 266109, China.

出版信息

Carbohydr Polym. 2025 Jan 15;348(Pt A):122852. doi: 10.1016/j.carbpol.2024.122852. Epub 2024 Oct 9.

Abstract

Pectin is a widely used natural emulsifier that is thought to stabilize emulsions in the upper gastrointestinal tract (GIT). However, changes in the structural characteristics and interfacial properties of pectin during its digestive treatment in the upper GIT and the effects on the stability of pectin-based emulsions are still unclear. This study showed that the stability of pectin-based emulsions steadily decreased in the upper GIT. Reductions in the molecular weight of pectin (from 2.74× 10 to 1.61× 10 g/mol) occurred mainly in the stomach, whereas the degree of esterification (from 61.2 % to 42.1 %) decreased throughout the digestive treatment. The change in the structure of pectin reduced its hydrophobicity in the upper GIT, and led to form a cross-linked network with Ca in small intestine rather than adsorbing to the oil-water interface. The behavior was reflected in the increased interfacial tension and the decreases in the interfacial modulus and thickness of pectin. Our insights into the structural characteristics and interfacial properties of pectin and thus into the mechanism of pectin instability in the upper GIT will contribute to the development of more efficient encapsulation methods and improved targeted delivery for active substances or probiotics using pectin-based emulsions.

摘要

果胶是一种广泛使用的天然乳化剂,被认为可以在上胃肠道 (GIT) 中稳定乳液。然而,果胶在其在上胃肠道消化处理过程中结构特性和界面性质的变化及其对果胶基乳液稳定性的影响仍不清楚。本研究表明,果胶基乳液在上胃肠道的稳定性逐渐下降。果胶的分子量(从 2.74×10 降至 1.61×10 g/mol)主要在胃中降低,而酯化度(从 61.2%降至 42.1%)在整个消化处理过程中降低。果胶结构的变化降低了其在上胃肠道的疏水性,并导致其在小肠中与 Ca 形成交联网络,而不是吸附在油水界面上。这种行为反映在界面张力增加,以及果胶的界面模量和厚度降低。我们对果胶的结构特性和界面性质的深入了解,以及果胶在上胃肠道不稳定的机制,将有助于开发更有效的包封方法,并提高使用果胶基乳液的活性物质或益生菌的靶向递送效率。

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