Single-Macromolecular Level Imaging of a Hydrogel Structure

R. Kiyama, T. Nonoyama, Sedlacik Tomas, H. Jinnai, J. Gong
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引用次数: 1

Abstract

Hydrogels are promising materials for several applications, including cell scaffolds and artificial load-bearing substitutes (cartilages, ligaments, tendons, etc.). Direct observation of the nanoscale polymer network of hydrogels is essential in understanding its properties. However, imaging of individual network strands at the molecular level is not achieved yet due to the lack of suitable methods. Herein, for the first time, we developed a novel mineral-staining method and network fixation method for transmission electron microscopy observation to visualize the hydrogel network in its unperturbed conformation with nanometer resolution. Surface network observation indicates that the length of surface dangling chains, which play a major role in friction and wetting, can be estimated from the gel mesh size. Moreover, bulk observations reveals a hierarchical formation mechanism of gel heterogeneity. These observations have the great potential to advance gel science by providing comprehensive perspective that link bulk gel properties with nanoscale.
水凝胶结构的单大分子水平成像
水凝胶是一种很有前途的材料,可用于多种用途,包括细胞支架和人工承重替代品(软骨、韧带、肌腱等)。直接观察纳米级水凝胶聚合物网络是了解其性质的必要条件。然而,由于缺乏合适的方法,单个网络链在分子水平上的成像尚未实现。在此,我们首次开发了一种新的矿物染色方法和网络固定方法,用于透射电子显微镜观察,以纳米分辨率显示水凝胶网络的无扰动构象。表面网络观测表明,在摩擦和润湿中起主要作用的表面悬垂链的长度可以通过凝胶网的大小来估计。此外,体积观察揭示了凝胶非均质性的分层形成机制。这些观察结果提供了将凝胶体性质与纳米尺度联系起来的全面视角,具有推动凝胶科学发展的巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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