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      Crack propagation in cortical bone is affected by the characteristics of the cement line: a parameter study using an XFEM interface damage model

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          Abstract

          Bulk properties of cortical bone have been well characterized experimentally, and potent toughening mechanisms, e.g., crack deflections, have been identified at the microscale. However, it is currently difficult to experimentally measure local damage properties and isolate their effect on the tissue fracture resistance. Instead, computer models can be used to analyze the impact of local characteristics and structures, but material parameters required in computer models are not well established. The aim of this study was therefore to identify the material parameters that are important for crack propagation in cortical bone and to elucidate what parameters need to be better defined experimentally. A comprehensive material parameter study was performed using an XFEM interface damage model in 2D to simulate crack propagation around an osteon at the microscale. The importance of 14 factors (material parameters) on four different outcome criteria (maximum force, fracture energy, crack length and crack trajectory) was evaluated using ANOVA for three different osteon orientations. The results identified factors related to the cement line to influence the crack propagation, where the interface strength was important for the ability to deflect cracks. Crack deflection was also favored by low interface stiffness. However, the cement line properties are not well determined experimentally and need to be better characterized. The matrix and osteon stiffness had no or low impact on the crack pattern. Furthermore, the results illustrated how reduced matrix toughness promoted crack penetration of the cement line. This effect is highly relevant for the understanding of the influence of aging on crack propagation and fracture resistance in cortical bone.

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          The online version of this article (10.1007/s10237-019-01142-4) contains supplementary material, which is available to authorized users.

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          Elastic crack growth in finite elements with minimal remeshing

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            The partition of unity finite element method: Basic theory and applications

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              Age-related changes in the plasticity and toughness of human cortical bone at multiple length scales.

              The structure of human cortical bone evolves over multiple length scales from its basic constituents of collagen and hydroxyapatite at the nanoscale to osteonal structures at near-millimeter dimensions, which all provide the basis for its mechanical properties. To resist fracture, bone's toughness is derived intrinsically through plasticity (e.g., fibrillar sliding) at structural scales typically below a micrometer and extrinsically (i.e., during crack growth) through mechanisms (e.g., crack deflection/bridging) generated at larger structural scales. Biological factors such as aging lead to a markedly increased fracture risk, which is often associated with an age-related loss in bone mass (bone quantity). However, we find that age-related structural changes can significantly degrade the fracture resistance (bone quality) over multiple length scales. Using in situ small-angle X-ray scattering and wide-angle X-ray diffraction to characterize submicrometer structural changes and synchrotron X-ray computed tomography and in situ fracture-toughness measurements in the scanning electron microscope to characterize effects at micrometer scales, we show how these age-related structural changes at differing size scales degrade both the intrinsic and extrinsic toughness of bone. Specifically, we attribute the loss in toughness to increased nonenzymatic collagen cross-linking, which suppresses plasticity at nanoscale dimensions, and to an increased osteonal density, which limits the potency of crack-bridging mechanisms at micrometer scales. The link between these processes is that the increased stiffness of the cross-linked collagen requires energy to be absorbed by "plastic" deformation at higher structural levels, which occurs by the process of microcracking.
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                Author and article information

                Contributors
                +46 (0) 46 222 0659 , anna.gustafsson@bme.lth.se
                mathias.wallin@solid.lth.se
                hanifeh.khayyeri@bme.lth.se
                hanna.isaksson@bme.lth.se
                Journal
                Biomech Model Mechanobiol
                Biomech Model Mechanobiol
                Biomechanics and Modeling in Mechanobiology
                Springer Berlin Heidelberg (Berlin/Heidelberg )
                1617-7959
                1617-7940
                8 April 2019
                8 April 2019
                2019
                : 18
                : 4
                : 1247-1261
                Affiliations
                [1 ]ISNI 0000 0001 0930 2361, GRID grid.4514.4, Department of Biomedical Engineering, , Lund University, ; Box 118, 221 00 Lund, Sweden
                [2 ]ISNI 0000 0001 0930 2361, GRID grid.4514.4, Division of Solid Mechanics, , Lund University, ; Box 118, 221 00 Lund, Sweden
                Author information
                http://orcid.org/0000-0002-5735-9503
                http://orcid.org/0000-0002-9107-5993
                http://orcid.org/0000-0001-5751-3737
                http://orcid.org/0000-0002-9690-8907
                Article
                1142
                10.1007/s10237-019-01142-4
                6647448
                30963356
                b4439749-f918-43c9-a2c3-ed027b72dfad
                © The Author(s) 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

                History
                : 15 November 2018
                : 22 March 2019
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001729, Stiftelsen för Strategisk Forskning;
                Award ID: IB2013-0021
                Award Recipient :
                Categories
                Original Paper
                Custom metadata
                © Springer-Verlag GmbH Germany, part of Springer Nature 2019

                Biophysics
                osteons,fracture toughness,crack deflection,interface,microstructure
                Biophysics
                osteons, fracture toughness, crack deflection, interface, microstructure

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