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dc.contributor.authorLiu, Yankai
dc.date.accessioned2012-02-15T10:04:00Z
dc.date.available2012-02-15T10:04:00Z
dc.date.issued2012
dc.identifier.urihttp://qmro.qmul.ac.uk/xmlui/handle/123456789/2409
dc.descriptionPhDen_US
dc.description.abstractBiological tissues maintain their homeostasis by remodelling under external mechanical stimuli. In order to understand the tissue remodelling process, it is important to characterize tissue properties before detailed mechanical responses can be investigated. This project aims to develop a computational modelling framework to characterise mechanical properties of biological tissues, and to quantify tissue responses under mechanical loading. The thesis presents, first, mechanical responses of articular cartilages under different loadings using a poroelastic model. Unique in this study, collagen fibrils are treated separately from the rest of ECM, as they only resists tension. This leads to a fibril-reinforced poroelastic model. Effects of the distribution of the collagen fibrils and their orientation on tissue mechanical responses are investigated. Most of the effort has been on the mechanical stress distribution of the human left atrium and its correlation to electrophysiology patterns in atrial fibrillation. Detailed mechanical responses of the atrial wall to a step pressure increase in the left atrium are calculated. The geometry of the left atrium is based on patient specific images using cardio CT and incorporates variations of the atrial wall thickness as well as unique fibre orientation patterns. We hypothesize that areas of high von Mises stress are correlated to foci of abnormal electrophysiology sites which sustain cardiac arrhythmia. Results from this study show a positive correlation between them. To our knowledge, this is the first study that establishes the relationship between the atrial wall stress distribution and the atrial abnormal electrophysiology sites. The project also investigates hyperelastic properties of endothelial cells and the overlying endothelial glycocalyx, based on data from AFM micro-indentation. Both endothelial cells with & without the glycocalyx layer (i.e. following enzymatic digestion) are used. This is the first time that the mechanical property of the glycocalyx is estimated using an inverse biomechanical model.en_US
dc.language.isoenen_US
dc.publisherQueen Mary University of London
dc.subjectBiochemistryen_US
dc.subjectExperimental autoimmune encephalomyelitisen_US
dc.subjectFatty acid amide hydrolaseen_US
dc.subjectFAAHen_US
dc.subjectCannabinoidsen_US
dc.titleModelling studies on biological tissue properties and mechanical responses under external stimulien_US
dc.typeThesisen_US
dc.rights.holderThe copyright of this thesis rests with the author and no quotation from it or information derived from it may be published without the prior written consent of the author


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    Theses Awarded by Queen Mary University of London

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