Formation mechanism of anisotropic gelatin hydrogel by self-assembly on oriented templates†

IF 3.2 3区 工程技术 Q2 CHEMISTRY, PHYSICAL
Kohei Kawaguchi, Tamaki Maeda, Syuuhei Komatsu, Yoshihiro Nomura and Kazuki Murai
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Abstract

The development of structurally controlled techniques inspired by the structural formation of living systems is of great importance for the fabrication of next-generation functional soft materials using environmentally friendly processes. This study aimed to investigate the formation mechanism of anisotropic structures of the gelatin network in a hydrogel through self-assembly on oriented templates. The effects of the oriented template having a uniaxially oriented surface on the anisotropic structure of the gelatin network were influenced by the structure at different scales: molecular (the secondary structure as the microstructure on the gelatin molecule) and molecular-assembled (the morphology of the gelatin network) scales. The mechanical properties and swelling behavior of the prepared gelatin hydrogels were characterized based on the anisotropic gelatin networks. The formation of an anisotropic gelatin network by self-assembly on the oriented template was presumably achieved by a two-step process due to the following two types of structural control factors: (1) the strength of the interaction between the template and gelatin molecules, and (2) the phase separation between the gelatin and water molecules induced during the hydrogelation process. The first process involves the formation of a thin molecular layer by the interaction between the template and gelatin molecules. The second process involves phase separation between the gelatin and water molecules during the cooling process of hydrogelation. These structurally controlled techniques for the formation of polymer networks inspired by biomineralization have two application prospects, which are the construction of biological tissue-like soft materials with complex hierarchical and anisotropic network structures through self-assembly processes, and expression of biological tissue-like functions.

Abstract Image

各向异性明胶水凝胶在定向模板上自组装的形成机理
开发受生命系统结构形成启发的结构控制技术,对于利用环境友好型工艺制作下一代功能性软材料具有重要意义。本研究旨在通过定向模板上的自组装,研究水凝胶中明胶网络各向异性结构的形成机制。定向模板对明胶网络各向异性结构的影响受不同尺度结构的影响:分子尺度(作为明胶分子微观结构的二级结构)和分子组装尺度(明胶网络的形态)。根据各向异性明胶网络,对制备的明胶水凝胶的机械性能和溶胀行为进行了表征。在定向模板上通过自组装形成各向异性明胶网络可能是由以下两类结构控制因素分两步实现的:(1) 模板与明胶分子之间相互作用的强度,以及 (2) 水凝胶化过程中明胶与水分子之间的相分离。第一个过程是通过模板和明胶分子之间的相互作用形成薄分子层。第二个过程涉及水凝胶冷却过程中明胶分子和水分子之间的相分离。
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来源期刊
Molecular Systems Design & Engineering
Molecular Systems Design & Engineering Engineering-Biomedical Engineering
CiteScore
6.40
自引率
2.80%
发文量
144
期刊介绍: Molecular Systems Design & Engineering provides a hub for cutting-edge research into how understanding of molecular properties, behaviour and interactions can be used to design and assemble better materials, systems, and processes to achieve specific functions. These may have applications of technological significance and help address global challenges.
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