Virtual testing methodology to predict the mechanical behavior of collagen hydrogels from nanoarchitecture

IF 8.7 1区 医学 Q1 ENGINEERING, BIOMEDICAL
Elías Núñez-Ortega , Pablo Blázquez-Carmona , Raquel Ruiz-Mateos , José E. Martín-Alfonso , José A. Sanz-Herrera , Esther Reina-Romo
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Abstract

Collagen-based hydrogels are three-dimensional, cross-linked structures capable of mimicking the extracellular fibered matrix of biological tissues, making them particularly well-suited for biomedical applications. These hydrogels typically exhibit highly non-linear mechanical behavior, which strongly depends on their internal nanostructural characteristics - an interconnection that remains poorly understood. The aim of this work is to combine high resolution imaging with a multiscale in silico structural model to virtually reproduce the mechanical behavior of a widely used collagen-based hydrogel, using solely its nanoarchitecture as input. The real fiber structure of the hydrogel was originally quantified at the nanometer scale using state-of-the-art microscopy, specifically, focused ion beam-scanning electron microscopy (FIB-SEM). In silico shear tests were then performed on the reconstructed collagen matrix to compute, through a multiscale approach, its homogenized mechanical response, including the energies and stresses developed by the fibers during the tests. Different samples of the hydrogel were also mechanically characterized by means of rheological tests to fit the model and show the feasibility of the methodology. The in silico simulations successfully captured the detailed mechanical interactions between fibers as well as the experimental non-linear mechanical behavior of the hydrogels. Results also highlight the relevant role of the bending energy throughout the entire range of deformation analyzed. This methodology provides a framework to elucidate the structure-mechanical behavior relationship of fiber network topologies, and can be applied to predict mechanical response of both native tissues and biomaterials based exclusively on their fibered nanostructures.
从纳米结构预测胶原水凝胶力学行为的虚拟测试方法
基于胶原蛋白的水凝胶是三维的,交联的结构,能够模拟生物组织的细胞外纤维基质,使其特别适合生物医学应用。这些水凝胶通常表现出高度非线性的力学行为,这在很大程度上取决于它们内部的纳米结构特征——这种相互联系仍然知之甚少。这项工作的目的是将高分辨率成像与多尺度硅结构模型相结合,以虚拟再现广泛使用的胶原基水凝胶的力学行为,仅使用其纳米结构作为输入。水凝胶的真实纤维结构最初是在纳米尺度上使用最先进的显微镜,特别是聚焦离子束扫描电子显微镜(FIB-SEM)进行量化的。然后对重建的胶原蛋白基质进行硅剪切试验,通过多尺度方法计算其均质力学响应,包括纤维在试验过程中产生的能量和应力。通过流变试验对不同的水凝胶样品进行了力学表征,以拟合模型,并证明了该方法的可行性。计算机模拟成功地捕获了纤维之间的详细力学相互作用以及水凝胶的非线性力学行为。结果还突出了弯曲能在整个变形分析范围内的相关作用。该方法为阐明纤维网络拓扑结构的结构-力学行为关系提供了一个框架,并且可以应用于仅基于其纤维纳米结构的天然组织和生物材料的力学响应预测。
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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来源期刊
CiteScore
8.30
自引率
4.90%
发文量
303
审稿时长
30 days
期刊介绍: Materials Today Bio is a multidisciplinary journal that specializes in the intersection between biology and materials science, chemistry, physics, engineering, and medicine. It covers various aspects such as the design and assembly of new structures, their interaction with biological systems, functionalization, bioimaging, therapies, and diagnostics in healthcare. The journal aims to showcase the most significant advancements and discoveries in this field. As part of the Materials Today family, Materials Today Bio provides rigorous peer review, quick decision-making, and high visibility for authors. It is indexed in Scopus, PubMed Central, Emerging Sources, Citation Index (ESCI), and Directory of Open Access Journals (DOAJ).
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