Numerical modelling of cancellous bone damage using an orthotropic failure criterion and tissue elastic properties as a function of the mineral content and microporosity.

Cancellous bone numerical modelling Damage initiation Finite element method Lamellar bone porosity Material property degradation Orthotropic failure criterion

Journal

Computer methods and programs in biomedicine
ISSN: 1872-7565
Titre abrégé: Comput Methods Programs Biomed
Pays: Ireland
ID NLM: 8506513

Informations de publication

Date de publication:
Jun 2022
Historique:
received: 22 09 2021
revised: 07 03 2022
accepted: 18 03 2022
pubmed: 3 4 2022
medline: 11 5 2022
entrez: 2 4 2022
Statut: ppublish

Résumé

Elastic and strength properties of lamellar tissue are essential to analyze the mechanical behaviour of bone at the meso- or macro-scale. Although many efforts have been made to model the architecture of cancellous bone, in general, isotropic elastic constants are assumed for tissue modelling, neglecting its non-isotropic behaviour. Therefore, isotropic damage laws are often used to estimate the bone failure. The main goals of this work are: (1) to present a new model for the estimation of the elastic properties of lamellar tissue which includes the bone mineral density (BMD) and the microporosity, (2) to address the numerical modelling of cancellous bone damage using an orthotropic failure criterion and a discrete damage mechanics analysis, including the novel approach for the tissue elastic properties aforementioned. Numerical homogenization has been used to estimate the elastic properties of lamellar bone considering BMD and microporosity. Microcomputed Tomography (μ-CT) scans have been performed to obtain the micro-finite element (μ-FE) model of cancellous bone from a vertebra of swine. In this model, lamellar tissue is orientated by considering a unidirectional layer pattern being the mineralized collagen fibrils aligned with the most representative geometrical feature of the trabeculae network. We have considered the Hashin's failure criterion and the Material Property Degradation (MPDG) method for simulating the onset and evolution of bone damage. The terms of the stiffness matrix for lamellar tissue are derived as functions of the BMD and microporosity at tissue scale. Results obtained for the apparent yield strain values agree with experimental values found in the literature. The influence of the damage parameters on the bone mechanics behaviour is also presented. Stiffness matrix of lamellar tissue depends on both BMD and microporosity. The new approach presented in this work enables to analyze the influence of the BMD and porosity on the mechanical response of bone. Lamellar tissue orientation has to be considered in the mechanical analysis of the cancellous bone. An orthotropic failure criterion can be used to analyze the bone failure onset instead of isotropic criteria. The elastic property degradation method is an efficient procedure to analyze the failure propagation in a 3D numerical model.

Sections du résumé

BACKGROUND AND OBJECTIVE OBJECTIVE
Elastic and strength properties of lamellar tissue are essential to analyze the mechanical behaviour of bone at the meso- or macro-scale. Although many efforts have been made to model the architecture of cancellous bone, in general, isotropic elastic constants are assumed for tissue modelling, neglecting its non-isotropic behaviour. Therefore, isotropic damage laws are often used to estimate the bone failure. The main goals of this work are: (1) to present a new model for the estimation of the elastic properties of lamellar tissue which includes the bone mineral density (BMD) and the microporosity, (2) to address the numerical modelling of cancellous bone damage using an orthotropic failure criterion and a discrete damage mechanics analysis, including the novel approach for the tissue elastic properties aforementioned.
METHODS METHODS
Numerical homogenization has been used to estimate the elastic properties of lamellar bone considering BMD and microporosity. Microcomputed Tomography (μ-CT) scans have been performed to obtain the micro-finite element (μ-FE) model of cancellous bone from a vertebra of swine. In this model, lamellar tissue is orientated by considering a unidirectional layer pattern being the mineralized collagen fibrils aligned with the most representative geometrical feature of the trabeculae network. We have considered the Hashin's failure criterion and the Material Property Degradation (MPDG) method for simulating the onset and evolution of bone damage.
RESULTS RESULTS
The terms of the stiffness matrix for lamellar tissue are derived as functions of the BMD and microporosity at tissue scale. Results obtained for the apparent yield strain values agree with experimental values found in the literature. The influence of the damage parameters on the bone mechanics behaviour is also presented.
CONCLUSIONS CONCLUSIONS
Stiffness matrix of lamellar tissue depends on both BMD and microporosity. The new approach presented in this work enables to analyze the influence of the BMD and porosity on the mechanical response of bone. Lamellar tissue orientation has to be considered in the mechanical analysis of the cancellous bone. An orthotropic failure criterion can be used to analyze the bone failure onset instead of isotropic criteria. The elastic property degradation method is an efficient procedure to analyze the failure propagation in a 3D numerical model.

Identifiants

pubmed: 35366593
pii: S0169-2607(22)00150-X
doi: 10.1016/j.cmpb.2022.106764
pii:
doi:

Substances chimiques

Minerals 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106764

Informations de copyright

Copyright © 2022 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Raquel Megías (R)

Dept. de Ingeniería Mecánica y de Materiales. Instituto de Ingeniería Mecánica y Biomecánica de Valencia - I2MB, Universitat Politècnica de València, Camino de Vera, Building 5E-9C, Valencia 46022, Spain.

Ana Vercher-Martínez (A)

Dept. de Ingeniería Mecánica y de Materiales. Instituto de Ingeniería Mecánica y Biomecánica de Valencia - I2MB, Universitat Politècnica de València, Camino de Vera, Building 5E-9C, Valencia 46022, Spain. Electronic address: anvermar@dimm.upv.es.

Ricardo Belda (R)

Dept. de Ingeniería Mecánica y de Materiales. Instituto de Ingeniería Mecánica y Biomecánica de Valencia - I2MB, Universitat Politècnica de València, Camino de Vera, Building 5E-9C, Valencia 46022, Spain.

José Luis Peris (JL)

Instituto de Ingeniería Mecánica y Biomecánica de Valencia - I2MB, Healthcare Technology Group (GTS-IBV), Universitat Politècnica de València, Camino de Vera, Building 5E-9C, Valencia 46022, Spain.

Ricardo Larrainzar-Garijo (R)

Orthopedic and Trauma Department, Hospital Universitario Infanta Leonor, Medical School, Universidad Complutense Madrid, Spain.

Eugenio Giner (E)

Dept. de Ingeniería Mecánica y de Materiales. Instituto de Ingeniería Mecánica y Biomecánica de Valencia - I2MB, Universitat Politècnica de València, Camino de Vera, Building 5E-9C, Valencia 46022, Spain.

F Javier Fuenmayor (FJ)

Dept. de Ingeniería Mecánica y de Materiales. Instituto de Ingeniería Mecánica y Biomecánica de Valencia - I2MB, Universitat Politècnica de València, Camino de Vera, Building 5E-9C, Valencia 46022, Spain.

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Classifications MeSH