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dc.contributor.authorConnizzo, Brianne K
dc.contributor.authorGrodzinsky, Alan J
dc.date.accessioned2018-09-13T14:16:06Z
dc.date.available2018-09-13T14:16:06Z
dc.date.issued2017-01
dc.identifier.issn0021-9290
dc.identifier.urihttp://hdl.handle.net/1721.1/117737
dc.description.abstractTendons transmit load from muscle to bone by utilizing their unique static and viscoelastic tensile properties. These properties are highly dependent on the composition and structure of the tissue matrix, including the collagen I hierarchy, proteoglycans, and water. While the role of matrix constituents in the tensile response has been studied, their role in compression, particularly in matrix pressurization via regulation of fluid flow, is not well understood. Injured or diseased tendons and tendon regions that naturally experience compression are known to have alterations in glycosaminoglycan content, which could modulate fluid flow and ultimately mechanical function. While recent theoretical studies have predicted tendon mechanics using poroelastic theory, no experimental data have directly demonstrated such behavior. In this study, we use high-bandwidth AFM-based rheology to determine the dynamic response of tendons to compressive loading at the nanoscale and to determine the presence of poroelastic behavior. Tendons are found to have significant characteristic dynamic relaxation behavior occurring at both low and high frequencies. Classic poroelastic behavior is observed, although we hypothesize that the full dynamic response is caused by a combination of flow-dependent poroelasticity as well as flow-independent viscoelasticity. Tendons also demonstrate regional dependence in their dynamic response, particularly near the junction of tendon and bone, suggesting that the structural and compositional heterogeneity in tendon may be responsible for regional poroelastic behavior. Overall, these experiments provide the foundation for understanding fluid-flow-dependent poroelastic mechanics of tendon, and the methodology is valuable for assessing changes in tendon matrix compressive behavior at the nanoscale. Keywords: Poroelasticity; Viscoelasticity; Tendon; AFM; Nanomechanicsen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant F32-AG052284)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Grant CMMI-1536233)en_US
dc.publisherElsevier BVen_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/J.JBIOMECH.2017.01.029en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleTendon exhibits complex poroelastic behavior at the nanoscale as revealed by high-frequency AFM-based rheologyen_US
dc.typeArticleen_US
dc.identifier.citationConnizzo, Brianne K., and Alan J. Grodzinsky. “Tendon Exhibits Complex Poroelastic Behavior at the Nanoscale as Revealed by High-Frequency AFM-Based Rheology.” Journal of Biomechanics 54 (March 2017): 11–18 © 2017 Elsevier Ltden_US
dc.contributor.departmentMassachusetts Institute of Technology. Center for Biomedical Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Mechanical Engineeringen_US
dc.contributor.mitauthorConnizzo, Brianne K
dc.contributor.mitauthorGrodzinsky, Alan J
dc.relation.journalJournal of Biomechanicsen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2018-09-06T15:58:01Z
dspace.orderedauthorsConnizzo, Brianne K.; Grodzinsky, Alan J.en_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-4942-3456
mit.licensePUBLISHER_CCen_US


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