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采用拉伸脱水策略构建各向异性且坚固的多糖基水凝胶:海藻酸钠、果胶、结冷胶和凝胶多糖的影响

Constructing anisotropic and strong polysaccharide-based hydrogels with stretching-dehydration strategy: Effect of sodium alginate, pectin, gellan gum, and curdlan.

作者信息

He Jun, Zhao Jingwen, Jia Wenzhe, Cui Yi, Wei Siyu, Zhao Yiguo, Fang Yapeng

机构信息

Department of Food Science and Engineering, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.

Department of Food Science and Engineering, School of Agriculture and Biology, Shanghai Jiao Tong University, Shanghai 200240, China.

出版信息

Carbohydr Polym. 2025 Jul 1;359:123567. doi: 10.1016/j.carbpol.2025.123567. Epub 2025 Apr 1.

DOI:10.1016/j.carbpol.2025.123567
PMID:40306775
Abstract

Polysaccharide-based hydrogels are widely utilized in the food industry and materials science due to their safety and abundance from natural sources. However, their functionality is often limited by poor mechanical properties, primarily due to their simple and isotropic structures. In this study, the stretching-dehydration (SD) processing was applied to create anisotropic structure and enhance the mechanical properties in polysaccharide-based hydrogels, specifically sodium alginate (SA), pectin (PE), gellan gum (GG), and curdlan (CU). Among these, low molecular weight sodium alginate (SA-L) hydrogel exhibited notable stretching-induced anisotropy and structural stability during dehydration. Furthermore, increasing the controlled strains (CSN) could improve anisotropy, stretching strength, and Young's modulus which reached up to 100 MPa in anisotropic SA-L hydrogel. The anisotropic hydrogels closely mimicked the microstructure of whole-muscle foods. Sensory evaluations highlighted the enhanced chewiness and hardness, suggesting the anisotropic hydrogels are promising candidates for emulating whole-muscle textures. This work highlights the potential of anisotropic hydrogels produced through simple SD treatment as advanced materials for both food and biomimetic applications.

摘要

基于多糖的水凝胶因其天然来源的安全性和丰富性而在食品工业和材料科学中得到广泛应用。然而,它们的功能往往受到机械性能差的限制,这主要是由于其简单且各向同性的结构。在本研究中,采用拉伸脱水(SD)工艺来创建各向异性结构并增强基于多糖的水凝胶的机械性能,具体包括海藻酸钠(SA)、果胶(PE)、结冷胶(GG)和凝胶多糖(CU)。其中,低分子量海藻酸钠(SA-L)水凝胶在脱水过程中表现出显著的拉伸诱导各向异性和结构稳定性。此外,增加控制应变(CSN)可以改善各向异性、拉伸强度和杨氏模量,在各向异性SA-L水凝胶中,杨氏模量可达100MPa。各向异性水凝胶紧密模仿了全肌肉食品的微观结构。感官评价突出了其增强的咀嚼性和硬度,表明各向异性水凝胶是模拟全肌肉质地的有前途的候选材料。这项工作突出了通过简单的SD处理生产的各向异性水凝胶作为食品和仿生应用的先进材料的潜力。

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