Abstract

Collagen network is one of the articular cartilage (AC) vital components, which contributes to the depth-dependent and anisotropic response of the tissue. As it is computationally expensive to simulate all the structural details of the AC network, they were typically simplified in numerical analysis. In particular, the so-called arcade-like structure, which has been widely used in the previous complex simulations, does not capture the rotations of the fibrillar bundles. In this study, we investigate the role of such possible rotations in the AC mechanical response by a set of advanced, biphasic, and parametric finite element (FE) simulations of indentation tests. Our results unveil the influence of fibrillar rotation (FR) on the mechanical response by increasing the fibrillar stress while regionally affecting the stress in the upper layers of the AC tissue. On the contrary, the FR did not significantly alter the tissue elasticity, and consequently might be ignored safely in pure contact mechanical problems. It is concluded that the excessive FR might regionally increase the stress, which can have a degenerative effect on the collagen constituent, and therefore, should not be neglected in the corresponding future studies, in which the upper AC layers resist high permanent shear strains.

Highlights

  • Articular Cartilage (AC) is an essential tissue of human knee joints consisting of several discrete components that play a vital role in knee functions by allowing the nearly frictionless motion between the contacting surfaces [1,2]

  • This study employed a parametric Finite Element (FE) simulation in order to determine the role of Fibrillar Rotations (FRs) in the AC biomechanical response

  • The results highlighted the role of FR in elasticity and stress distributions of AC, which could be used to estimate the signi cance of FR mechanical response at di erent scales

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Summary

Introduction

Articular Cartilage (AC) is an essential tissue of human knee joints consisting of several discrete components that play a vital role in knee functions by allowing the nearly frictionless motion between the contacting surfaces [1,2]. Accurate modeling of the collagen network is an essential step in most of the AC simulations. A variety of constitutive equations have been developed to address the AC brillar response [4{8]. Those models could thoroughly simulate the brillar part of AC, they are numerically, too expensive to be implemented [9]. Some of these previous studies [10{14] assumed that primary brils were located on planar surfaces, perpendicular to the AC surface. Intersection of those surfaces and the AC surface could form a de-

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