Influence of loading condition and anatomical location on human cortical bone linear micro-cracks.


Journal

Journal of biomechanics
ISSN: 1873-2380
Titre abrégé: J Biomech
Pays: United States
ID NLM: 0157375

Informations de publication

Date de publication:
06 03 2019
Historique:
received: 29 08 2018
revised: 02 01 2019
accepted: 03 01 2019
pubmed: 29 1 2019
medline: 25 3 2020
entrez: 29 1 2019
Statut: ppublish

Résumé

Human cortical bone fracture toughness depends on the anatomical locations under quasi-static loading. Recent results also showed that under fall-like loading, cortical bone fracture toughness is similar at different anatomical locations in the same donor. While cortical bone toughening mechanisms are known to be dependent on the tissue architecture under quasi-static loading, the fracture mechanisms during a fall are less studied. In the current study, the structural parameters of eight paired femoral diaphyses, femoral necks and radial diaphyses were mechanically tested under quasi-static and fall-like loading conditions (female donors, 70 ± 14 y.o., [50-91 y.o.]). Synchrotron radiation micro-CT imaging was used to quantify the amount of micro-cracks formed during loading. The volume fraction of these micro-cracks was significantly higher within the specimens loaded under a quasi-static condition than under a loading representative of a fall. Under fall-like loading, there was no difference in crack volume fraction between the different paired anatomical locations. This result shows that the micro-cracking toughening mechanism depends both on the anatomical location and on the loading condition.

Identifiants

pubmed: 30686510
pii: S0021-9290(19)30037-5
doi: 10.1016/j.jbiomech.2019.01.008
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

59-66

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Rémy Gauthier (R)

Univ Lyon, Université Claude Bernard Lyon 1, IFSTTAR, LBMC UMR_T9406, F69622 Lyon, France; Univ Lyon, CNRS UMR 5220, Inserm U1206, INSA Lyon, Université Claude Bernard Lyon 1, Creatis, F69621 Villeurbanne Cedex, France.

Max Langer (M)

Univ Lyon, CNRS UMR 5220, Inserm U1206, INSA Lyon, Université Claude Bernard Lyon 1, Creatis, F69621 Villeurbanne Cedex, France.

Hélène Follet (H)

Univ Lyon, Université Claude Bernard Lyon 1, INSERM, LYOS UMR1033, F69008 Lyon, France.

Cécile Olivier (C)

Univ Lyon, CNRS UMR 5220, Inserm U1206, INSA Lyon, Université Claude Bernard Lyon 1, Creatis, F69621 Villeurbanne Cedex, France; European Synchrotron Radiation Facility, CS 40220, 38043 Grenoble Cedex 9, France.

Pierre-Jean Gouttenoire (PJ)

Univ Lyon, CNRS UMR 5220, Inserm U1206, INSA Lyon, Université Claude Bernard Lyon 1, Creatis, F69621 Villeurbanne Cedex, France; European Synchrotron Radiation Facility, CS 40220, 38043 Grenoble Cedex 9, France.

Lukas Helfen (L)

European Synchrotron Radiation Facility, CS 40220, 38043 Grenoble Cedex 9, France; Institute for Photon Science and Synchrotron Radiation, Karlsruhe Institute of Technology (KIT), D-76131 Karlsruhe, Germany.

Frédéric Rongiéras (F)

Univ Lyon, Université Claude Bernard Lyon 1, IFSTTAR, LBMC UMR_T9406, F69622 Lyon, France; Service Chirurgie Orthopédique et Traumatologie - Hôpital Desgenettes, 69003 Lyon, France.

David Mitton (D)

Univ Lyon, Université Claude Bernard Lyon 1, IFSTTAR, LBMC UMR_T9406, F69622 Lyon, France.

Françoise Peyrin (F)

Univ Lyon, CNRS UMR 5220, Inserm U1206, INSA Lyon, Université Claude Bernard Lyon 1, Creatis, F69621 Villeurbanne Cedex, France; European Synchrotron Radiation Facility, CS 40220, 38043 Grenoble Cedex 9, France. Electronic address: peyrin@esrf.fr.

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Classifications MeSH