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dc.contributor.authorBell, James S.en_GB
dc.date.accessioned2011-05-13T16:11:18Zen_GB
dc.date.accessioned2013-03-21T13:05:11Z
dc.date.issued2011-01-04en_GB
dc.description.abstractArticular cartilage (AC) is a soft connective tissue that lines the ends of synovial bones in joints. It is responsible for absorbing impact loads and resisting shear associated with joint articulation. Pathologies such as osteoarthritis have symptoms including degradation and sometimes complete loss of the articular cartilage, which can lead to poor load support and considerable pain. There has been considerable work in the field of cartilage mechanics. The transient deformation behaviour of loaded cartilage has been examined using several different experimental approaches, and complex models have been developed to accurately describe this behaviour. The microstructural response of AC to load is less well understood, however. The aim of this work was to investigate the anisotropy and heterogeneity of cartilage and its effect on the load bearing characteristics. Firstly, existing experimental data were used to create a layered finite element model of cartilage under load. Using this model, three sets of material parameters were evaluated for their suitability in reproducing experimentally observed strains, as well as minimising peak stresses. It was found that only by including the heterogeneity associated with collagen fibre orientation could the layer boundary deformations be exactly modelled, whilst preventing potentially damaging interfacial shear. Tensile testing of cartilage from the equine metacarpophalangeal joint, using samples obtained from each individual layer, was performed to validate findings from the model as well as to determine the variation in mechanical properties in regions of different weight bearing characteristics. It was found that the tensile stiffnesses varied with depth as predicted by the model, demonstrating an average value of 31.3 MPa at the surface and 9.4 MPa in the radial zone, although there was considerable variation. Polarised light microscopy was used to determine the preferential collagen orientation, as well as qualitatively assess the angular spread and other patterns in collagen organisation. It was found that the appearance of the collagen network varied both with depth and location on the joint, with high weight bearing regions showing more isotropic fibre distributions below the surface than low weight bearing regions. To directly probe the microstructural response of AC to load, the tensile loading rig was modified to allow simultaneous imaging of the sample using two photon fluorescence microscopy. This allowed the relative displacement of cells and elastin fibres, which are intrinsically fluorescent, to be observed at increasing levels of strain. From locations and orientations of these features, the strain field could be calculated at two length scales: in the vicinity of specific elastin fibres (microns) and intercellular strains averaged over whole stacks (hundreds of microns). The strains at the two different scales did not correlate, suggesting that the microscopic strain environment varies considerably. The elastin fibre network was also investigated, and it was found that fibres appear to interconnect both at pericellular matrices, as well as at 'nodes' in the extracellular matrix.en_GB
dc.identifier.citationBell JS, Winlove CP, Smith CW, Dehghani H (2009) Modeling the steady-state deformation of the solid phase of articular cartilage. Biomaterials 30(31): 6394–6401en_GB
dc.identifier.urihttp://hdl.handle.net/10036/3082en_GB
dc.language.isoenen_GB
dc.publisherUniversity of Exeteren_GB
dc.rights.embargoreasonPublication of work.en_GB
dc.titleThe Relationship between the Composition and Mechanical Properties of Articular Cartilageen_GB
dc.typeThesis or dissertationen_GB
dc.date.available2012-11-30T05:00:04Zen_GB
dc.date.available2013-03-21T13:05:11Z
dc.contributor.advisorWinlove, C. Peteren_GB
dc.publisher.departmentPhysicsen_GB
dc.type.degreetitlePhD in Physicsen_GB
dc.type.qualificationlevelDoctoralen_GB
dc.type.qualificationnamePhDen_GB


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