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软组织疲劳:多尺度力学与本构建模。

Fatigue of soft fibrous tissues: Multi-scale mechanics and constitutive modeling.

机构信息

Department of Continuum Mechanics, RWTH Aachen University, Kackertstr. 9, 52072 Aachen, Germany.

Department of Continuum Mechanics, RWTH Aachen University, Kackertstr. 9, 52072 Aachen, Germany.

出版信息

Acta Biomater. 2018 Apr 15;71:398-410. doi: 10.1016/j.actbio.2018.03.010. Epub 2018 Mar 15.

Abstract

UNLABELLED

In recent experimental studies a possible damage mechanism of collagenous tissues mainly caused by fatigue was disclosed. In this contribution, a multi-scale constitutive model ranging from the tropocollagen (TC) molecule level up to bundles of collagen fibers is proposed and utilized to predict the elastic and inelastic long-term tissue response. Material failure of collagen fibrils is elucidated by a permanent opening of the triple helical collagen molecule conformation, triggered either by overstretching or reaction kinetics of non-covalent bonds. This kinetics is described within a probabilistic framework of adhesive detachments of molecular linkages providing collagen fiber integrity. Both intramolecular and interfibrillar linkages are considered. The final constitutive equations are validated against recent experimental data available in literature for both uniaxial tension to failure and the evolution of fatigue in subsequent loading cycles. All material parameters of the proposed model have a clear physical interpretation.

STATEMENT OF SIGNIFICANCE

Irreversible changes take place at different length scales of soft fibrous tissues under supra-physiological loading and alter their macroscopic mechanical properties. Understanding the evolution of those histologic pathologies under loading and incorporating them into a continuum mechanical framework appears to be crucial in order to predict long-term evolution of various diseases and to support the development of tissue engineering.

摘要

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在最近的实验研究中,揭示了胶原组织可能主要由疲劳引起的损伤机制。在本研究中,提出了一种从原胶原(TC)分子水平到胶原纤维束的多尺度本构模型,并用于预测弹性和非弹性的长期组织响应。胶原纤维的材料失效是通过永久打开三螺旋胶原分子构象来阐明的,这是由过度拉伸或非共价键的反应动力学触发的。这种动力学是在分子键的粘附有永久性分离的概率框架内描述的,提供了胶原纤维的完整性。考虑了分子内和纤维间的键合。最终的本构方程是针对文献中最近的实验数据进行验证的,这些数据包括单轴拉伸至失效以及随后加载循环中疲劳的演变。所提出模型的所有材料参数都具有明确的物理解释。

意义声明

在超生理负荷下,软纤维组织在不同的长度尺度上会发生不可逆的变化,从而改变其宏观力学性能。了解在加载下这些组织病理学的演变,并将其纳入连续体力学框架中,似乎对于预测各种疾病的长期演变以及支持组织工程的发展至关重要。

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