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Local stress-strain distribution and load transfer across cartilage matrix at micro-scale using combined microscopy-based finite element method

机译:基于组合显微镜的有限元方法在微观尺度上局部应力-应变分布和跨软骨基质的载荷转移

摘要

Articular cartilage is the load-bearing tissue that consists of proteoglycan macromolecules entrapped between collagen fibrils in a three-dimensional architecture. To date, the drudgery of searching for mathematical models to represent the biomechanics of such a system continues without providing a fitting description of its functional response to load at micro-scale level. We believe that the major complication arose when cartilage was first envisaged as a multiphasic model with distinguishable components and that quantifying those and searching for the laws that govern their interaction is inadequate. To the thesis of this paper, cartilage as a bulk is as much continuum as is the response of its components to the external stimuli. For this reason, we framed the fundamental question as to what would be the mechano-structural functionality of such a system in the total absence of one of its key constituents-proteoglycans. To answer this, hydrated normal and proteoglycan depleted samples were tested under confined compression while finite element models were reproduced, for the first time, based on the structural microarchitecture of the cross-sectional profile of the matrices. These micro-porous in silico models served as virtual transducers to produce an internal noninvasive probing mechanism beyond experimental capabilities to render the matrices micromechanics and several others properties like permeability, orientation etc. The results demonstrated that load transfer was closely related to the microarchitecture of the hyperelastic models that represent solid skeleton stress and fluid response based on the state of the collagen network with and without the swollen proteoglycans. In other words, the stress gradient during deformation was a function of the structural pattern of the network and acted in concert with the position-dependent compositional state of the matrix. This reveals that the interaction between indistinguishable components in real cartilage is superimposed by its microarchitectural state which directly influences macromechanical behavior.
机译:关节软骨是由蛋白质多糖大分子组成的承重组织,该蛋白质多糖以三维结构夹在胶原纤维之间。迄今为止,寻找数学模型以表示这种系统的生物力学的工作仍在继续,而没有提供其对微观水平负载的功能响应的恰当描述。我们认为,当软骨最初被设想为具有可区分成分的多相模型时,主要的并发症就出现了,并且量化这些成分并寻找控制它们相互作用的规律是不够的。就本文的论文而言,作为一个整体的软骨与其组成部分对外部刺激的反应一样多。因此,我们提出了一个基本问题,即在完全不存在其主要成分蛋白聚糖的情况下,这种系统的机械结构功能是什么。为了回答这个问题,在有限的压缩下测试了水合正常和蛋白聚糖耗竭的样品,同时首次基于矩阵横截面轮廓的结构微体系结构复制了有限元模型。这些微孔计算机模型用作虚拟换能器,以产生超出实验能力的内部非侵入性探测机制,从而使矩阵具有微机械特性以及诸如渗透性,取向等其他一些特性。结果表明,载荷传递与传感器的微体系结构密切相关。超弹性模型,代表具有和不具有溶胀蛋白聚糖的胶原网络状态,表示固体骨架应力和流体反应。换句话说,变形过程中的应力梯度是网络结构模式的函数,并与基体的位置相关成分状态协同作用。这表明,在实际软骨中,难以区分的成分之间的相互作用被直接影响宏观力学行为的微观结构状态所叠加。

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