Modal analysis of nanoindentation data, confirming that reduced bone turnover may cause increased tissue mineralization/elasticity.
Autor: | Pastrama MI; Institute for Mechanics of Materials and Structures, TU Wien - Vienna University of Technology, Vienna, Austria; KU Leuven, Department of Movement Sciences, Human Movement Biomechanics Research Group, Tervuursevest 101, 3001 Leuven, Belgium., Blanchard R; St Vincent's Department of Surgery, University of Melbourne, Melbourne, Australia., Clement JG; Melbourne Dental School, University of Melbourne, Melbourne, Australia., Pivonka P; St Vincent's Department of Surgery, University of Melbourne, Melbourne, Australia; School of Chemistry, Physics and Mechanical Engineering, Queensland University of Technology, Brisbane, Australia., Hellmich C; Institute for Mechanics of Materials and Structures, TU Wien - Vienna University of Technology, Vienna, Austria. Electronic address: christian.hellmich@tuwien.ac.at. |
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Jazyk: | angličtina |
Zdroj: | Journal of the mechanical behavior of biomedical materials [J Mech Behav Biomed Mater] 2018 Aug; Vol. 84, pp. 217-224. Date of Electronic Publication: 2018 May 26. |
DOI: | 10.1016/j.jmbbm.2018.05.014 |
Abstrakt: | It is widely believed that the activities of bone cells at the tissue scale not only govern the size of the vascular pore spaces (and hence, the amount of bone tissue available for actually carrying the loads), but also the characteristics of the extracellular bone matrix itself. In this context, increased mechanical stimulation (in mediolateral regions of human femora, as compared to anteroposterior regions) may lead to increased bone turnover, lower bone matrix mineralization, and therefore lower tissue modulus. On the other hand, resorption-only processes (in endosteal versus periosteal regions) may have the opposite effect. A modal analysis of nanoindentation data obtained on femurs from the Melbourne Femur Research Collection (MFRC) indeed confirms that bone is stiffer in endosteal regions compared to periosteal regions (E̅ (Copyright © 2018 Elsevier Ltd. All rights reserved.) |
Databáze: | MEDLINE |
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