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Microscale fiber network alignment affects macroscale failure behavior in simulated collagen tissue analogs.微观尺度纤维网络排列影响模拟胶原组织类似物的宏观失效行为。
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Mechanical behavior of collagen-fibrin co-gels reflects transition from series to parallel interactions with increasing collagen content.胶原蛋白-纤维蛋白共凝胶的力学行为反映了随着胶原蛋白含量增加,其相互作用从串联到并联的转变。
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Elastomeric electrospun polyurethane scaffolds: the interrelationship between fabrication conditions, fiber topology, and mechanical properties.弹性体电纺聚氨酯支架:制备条件、纤维拓扑结构与力学性能之间的相互关系。
Adv Mater. 2011 Jan 4;23(1):106-11. doi: 10.1002/adma.201003210.
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Characterization of the complete fiber network topology of planar fibrous tissues and scaffolds.平面纤维组织和支架的完整纤维网络拓扑结构的描述。
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3D reconstruction of histological sections: Application to mammary gland tissue.组织切片的三维重建:在乳腺组织中的应用。
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On the biomechanical function of scaffolds for engineering load-bearing soft tissues.论工程承重软组织支架的生物力学功能。
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Scale-dependent fiber kinematics of elastomeric electrospun scaffolds for soft tissue engineering.用于软组织工程的弹性电纺支架的纤维运动学的尺度依赖性。
J Biomed Mater Res A. 2010 Jun 1;93(3):1032-42. doi: 10.1002/jbm.a.32593.
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Computational predictions of the tensile properties of electrospun fibre meshes: effect of fibre diameter and fibre orientation.电纺纤维网拉伸性能的计算预测:纤维直径和纤维取向的影响。
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平面层状弹性纤维生物材料的几何表征与模拟

Geometric characterization and simulation of planar layered elastomeric fibrous biomaterials.

作者信息

Carleton James B, D'Amore Antonio, Feaver Kristen R, Rodin Gregory J, Sacks Michael S

机构信息

Center for Cardiovascular Simulation, Institute for Computational and Engineering Sciences, Department of Biomedical Engineering, University of Texas at Austin, Austin, TX 78712, USA.

McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA 15261, USA.

出版信息

Acta Biomater. 2015 Jan;12:93-101. doi: 10.1016/j.actbio.2014.09.049. Epub 2014 Oct 13.

DOI:10.1016/j.actbio.2014.09.049
PMID:25311685
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4274256/
Abstract

Many important biomaterials are composed of multiple layers of networked fibers. While there is a growing interest in modeling and simulation of the mechanical response of these biomaterials, a theoretical foundation for such simulations has yet to be firmly established. Moreover, correctly identifying and matching key geometric features is a critically important first step for performing reliable mechanical simulations. The present work addresses these issues in two ways. First, using methods of geometric probability, we develop theoretical estimates for the mean linear and areal fiber intersection densities for 2-D fibrous networks. These densities are expressed in terms of the fiber density and the orientation distribution function, both of which are relatively easy-to-measure properties. Secondly, we develop a random walk algorithm for geometric simulation of 2-D fibrous networks which can accurately reproduce the prescribed fiber density and orientation distribution function. Furthermore, the linear and areal fiber intersection densities obtained with the algorithm are in agreement with the theoretical estimates. Both theoretical and computational results are compared with those obtained by post-processing of scanning electron microscope images of actual scaffolds. These comparisons reveal difficulties inherent to resolving fine details of multilayered fibrous networks. The methods provided herein can provide a rational means to define and generate key geometric features from experimentally measured or prescribed scaffold structural data.

摘要

许多重要的生物材料是由多层网络状纤维组成的。虽然人们对这些生物材料力学响应的建模和模拟越来越感兴趣,但此类模拟的理论基础尚未牢固确立。此外,正确识别和匹配关键几何特征是进行可靠力学模拟至关重要的第一步。本工作通过两种方式解决这些问题。首先,使用几何概率方法,我们为二维纤维网络的平均线性和面积纤维交叉密度建立理论估计。这些密度用纤维密度和取向分布函数表示,这两者都是相对易于测量的属性。其次,我们开发了一种用于二维纤维网络几何模拟的随机游走算法,该算法可以准确再现规定的纤维密度和取向分布函数。此外,通过该算法获得的线性和面积纤维交叉密度与理论估计一致。理论和计算结果都与通过对实际支架的扫描电子显微镜图像进行后处理获得的结果进行了比较。这些比较揭示了解析多层纤维网络精细细节所固有的困难。本文提供的方法可以提供一种合理的手段,从实验测量或规定的支架结构数据中定义和生成关键几何特征。

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