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    An Integrated Finite-Element Approach to Mechanics, Transport and Biosynthesis in Tissue Engineering

    Source: Journal of Biomechanical Engineering:;2004:;volume( 126 ):;issue: 001::page 82
    Author:
    Bram G. Sengers
    ,
    Cees W. J. Oomens
    ,
    Frank P. T. Baaijens
    DOI: 10.1115/1.1645526
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: A finite-element approach was formulated, aimed at enabling an integrated study of mechanical and biochemical factors that control the functional development of tissue engineered constructs. A nonlinear biphasic displacement-velocity-pressure description was combined with adjective and diffusive solute transport, uptake and biosynthesis. To illustrate the approach we focused on the synthesis and transport of macromolecules under influence of fluid flow induced by cyclic compression. In order to produce net transport the effect of dispersion was investigated. An abstract representation of biosynthesis was employed, three cases were distinguished: Synthesis dependent on a limited small solute, synthesis dependent on a limited large solute and synthesis independent of solute transport. Results show that a dispersion model can account for augmented solute transport by cyclic compression and indicate the different sensitivity to loading that can be expected depending on the size of the limiting solute.
    keyword(s): Diffusion (Physics) , Fluids , Biological tissues , Finite element analysis , Compression , Tissue engineering , Cartilage , Deformation , Pressure , Fluid dynamics , Macromolecules , Frequency , Modeling AND Displacement ,
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      An Integrated Finite-Element Approach to Mechanics, Transport and Biosynthesis in Tissue Engineering

    URI
    http://yetl.yabesh.ir/yetl1/handle/yetl/129653
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    • Journal of Biomechanical Engineering

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    contributor authorBram G. Sengers
    contributor authorCees W. J. Oomens
    contributor authorFrank P. T. Baaijens
    date accessioned2017-05-09T00:12:22Z
    date available2017-05-09T00:12:22Z
    date copyrightFebruary, 2004
    date issued2004
    identifier issn0148-0731
    identifier otherJBENDY-26353#82_1.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/129653
    description abstractA finite-element approach was formulated, aimed at enabling an integrated study of mechanical and biochemical factors that control the functional development of tissue engineered constructs. A nonlinear biphasic displacement-velocity-pressure description was combined with adjective and diffusive solute transport, uptake and biosynthesis. To illustrate the approach we focused on the synthesis and transport of macromolecules under influence of fluid flow induced by cyclic compression. In order to produce net transport the effect of dispersion was investigated. An abstract representation of biosynthesis was employed, three cases were distinguished: Synthesis dependent on a limited small solute, synthesis dependent on a limited large solute and synthesis independent of solute transport. Results show that a dispersion model can account for augmented solute transport by cyclic compression and indicate the different sensitivity to loading that can be expected depending on the size of the limiting solute.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleAn Integrated Finite-Element Approach to Mechanics, Transport and Biosynthesis in Tissue Engineering
    typeJournal Paper
    journal volume126
    journal issue1
    journal titleJournal of Biomechanical Engineering
    identifier doi10.1115/1.1645526
    journal fristpage82
    journal lastpage91
    identifier eissn1528-8951
    keywordsDiffusion (Physics)
    keywordsFluids
    keywordsBiological tissues
    keywordsFinite element analysis
    keywordsCompression
    keywordsTissue engineering
    keywordsCartilage
    keywordsDeformation
    keywordsPressure
    keywordsFluid dynamics
    keywordsMacromolecules
    keywordsFrequency
    keywordsModeling AND Displacement
    treeJournal of Biomechanical Engineering:;2004:;volume( 126 ):;issue: 001
    contenttypeFulltext
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