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A multiscale synthesis: characterizing acute cartilage failure under an aggregate tibiofemoral joint loading

机译:多尺度合成:在综合胫骨聚合荷载作用下表征急性软骨衰竭

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摘要

Knee articular cartilage is characterized by a complex mechanical behavior, posing a challenge to develop an efficient and precise model. We argue that the cartilage damage, in general, can be traced to the fibril level as a plastic deformation, defined as micro-defects. To investigate these micro-defects, we have developed a detailed finite element model of the entire healthy tibiofemoral joint (TF) including a multiscale constitutive model which considers the structural hierarchies of the articular cartilage. The net model was simulated under physiological loading conditions to predict joint response under 2000 N axial compression and damage initiation under high axial loading (max 7 KN) when the TF joint flexed to 30 degrees. Computed results sufficiently agreed with earlier experimental and numerical studies. Further, initiation and propagation of damage in fibrils were computed at the tibial cartilage located mainly in the superficial and middle layers. Our simulation results also indicated that the stiffer the fibril is (higher cross-link densities), the higher the contact stress required to elicit a fibril yield and the higher the rate of yielding as a function of increased contact stress. To the best of our knowledge, this is the first model that combines macro-continuum joint mechanics and micromechanics at the tissue level. The computational construct presented here serves as a simulation platform to explore the interplay between acute cartilage damage and micromechanics characteristics at the tropocollagen level.
机译:膝关节关节软骨的特点是复杂的机械行为,构成了开发有效和精确的模型的挑战。我们认为软骨损坏通常可以作为塑性变形追踪到原纤维水平,定义为微缺陷。为了研究这些微缺陷,我们开发了一种详细的整体健康胫铁膜关节(TF)的有限元模型,包括多尺度本构模型,该模型考虑关节软骨的结构层次结构。当TF关节弯曲至30度时,在生理负载条件下模拟了在生理负载条件下预测2000 n轴向压缩和损伤启动下的关节响应和损坏。计算结果与前面的实验和数值研究充分达成了同意。此外,在主要位于浅表和中间层的胫骨软骨上计算原纤维损伤的启动和繁殖。我们的仿真结果表明,纤维纤维(交联密度较高),引发原纤维产率的接触应力越高,越高的接触应力的函数越高。据我们所知,这是第一个将宏观连续力学和微机械在组织水平上结合的模型。这里呈现的计算构建体用作仿真平台,用于探索急性软骨损坏和微机械特性在流罗胶原水平之间的相互作用。

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