Jenny Carlsson, Olivia Karlsson, Hanna Isaksson, Anna Gustafsson
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引用次数: 0
Abstract
Computational models are commonly used to investigate how the cortical bone microstructure affects fracture resistance; recently, phase-field models have been introduced for this purpose. However, experimentally measured material parameters for the microstructural tissues are lacking. Moreover, as no validation studies have been published, it remains unclear to what extent classical phase-field methods, assuming linear-elastic, brittle fracture, accurately represent bone. In this study, we address both these shortcomings by first applying a design-of-experiments methodology to calibrate a set of material parameters for a two-dimensional phase-field finite element model of bovine osteonal microstructure. This was achieved by comparing the outcomes from simulation to data from single-edge notched bending experiments on bovine osteonal bone and subsequent imaging of the crack path. Second, we used these parameters in new bone geometries to evaluate the parameters and the predictive performance of the model. Reasonable agreement was achieved between prediction and experiments in terms of peak load, crack initiation toughness and crack path. However, the model is unable to capture the experimentally observed gradual evolution of damage, leading to a nonlinear force response before the onset of visible crack extension. Nor does it capture the similarly observed increase in toughness with increasing crack length. These limitations are inherent to all classical phase-field methods since they originate from theories of brittle fracture, and alternative formulations are discussed. This is the first study attempting to validate classical phase-field methods in simulation of cortical bone fracture, and it highlights both potential and limitations to be addressed in future work.
期刊介绍:
Mechanics regulates biological processes at the molecular, cellular, tissue, organ, and organism levels. A goal of this journal is to promote basic and applied research that integrates the expanding knowledge-bases in the allied fields of biomechanics and mechanobiology. Approaches may be experimental, theoretical, or computational; they may address phenomena at the nano, micro, or macrolevels. Of particular interest are investigations that
(1) quantify the mechanical environment in which cells and matrix function in health, disease, or injury,
(2) identify and quantify mechanosensitive responses and their mechanisms,
(3) detail inter-relations between mechanics and biological processes such as growth, remodeling, adaptation, and repair, and
(4) report discoveries that advance therapeutic and diagnostic procedures.
Especially encouraged are analytical and computational models based on solid mechanics, fluid mechanics, or thermomechanics, and their interactions; also encouraged are reports of new experimental methods that expand measurement capabilities and new mathematical methods that facilitate analysis.