Study of human cortical bone and demineralized human cortical bone viscoelasticity
The knowledge of human bone viscoelasticity is an important issue for defining semirigid calcified tissues implants. A very sensitive technique was used to investigate bone viscoelasticity: the thermally stimulated creep method. A study of demineralized human bone was performed to determine the mole...
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Published in: | Journal of applied polymer science Vol. 79; no. 14; pp. 2527 - 2533 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
New York
John Wiley & Sons, Inc
01-04-2001
Wiley |
Subjects: | |
Online Access: | Get full text |
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Summary: | The knowledge of human bone viscoelasticity is an important issue for defining semirigid calcified tissues implants. A very sensitive technique was used to investigate bone viscoelasticity: the thermally stimulated creep method. A study of demineralized human bone was performed to determine the molecular origin of bone viscoelasticity. The thermally stimulated creep spectra of bone and demineralized bone, at the hydrated state, present a similar shape with one main retardation mode located at −133 and −120°C, respectively. This mode is shifted toward higher temperatures after dehydration, revealing the existence of another mode at around −155°C. The analysis of elementary spectra of bone and demineralized bone has shown that retardation times follow an Arrhenius equation, and that two compensation phenomena are observed with comparable compensation parameters. The first compensation phenomenon, which corresponds to the main retardation mode, was attributed to motions of water molecules located inside the collagen triple helix. The second compensation phenomenon, which reveals the existence of another relaxation mode at higher temperatures, was assigned to movements of hydrophilic side chains bound to water molecules. As for the mode observed at around −155°C, it was associated with motions of aliphatic side chains. Overall, bone viscoelasticity originates from the organic matrix. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 79: 2527–2533, 2001 |
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Bibliography: | istex:AA5D8994754F25E9ECB9EEA2FFBAF9BE897FCE07 ArticleID:APP1061 ark:/67375/WNG-4NVFFLRM-S ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0021-8995 1097-4628 |
DOI: | 10.1002/1097-4628(20010401)79:14<2527::AID-APP1061>3.0.CO;2-J |