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    A Recruitment Model of Tendon Viscoelasticity That Incorporates Fibril Creep and Explains Strain-Dependent Relaxation

    Source: Journal of Biomechanical Engineering:;2020:;volume( 142 ):;issue: 007
    Author:
    Shearer, Tom
    ,
    Parnell, William J.
    ,
    Lynch, Barbara
    ,
    Screen, Hazel R. C.
    ,
    David Abrahams, I.
    DOI: 10.1115/1.4045662
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Soft tissues exhibit complex viscoelastic behavior, including strain-rate dependence, hysteresis, and strain-dependent relaxation. In this paper, a model for soft tissue viscoelasticity is developed that captures all of these features and is based upon collagen recruitment, whereby fibrils contribute to tissue stiffness only when taut. We build upon existing recruitment models by additionally accounting for fibril creep and by explicitly modeling the contribution of the matrix to the overall tissue viscoelasticity. The fibrils and matrix are modeled as linear viscoelastic and each fibril has an associated critical strain (corresponding to its length) at which it becomes taut. The model is used to fit relaxation tests on three rat tail tendon fascicles and predict their response to cyclic loading. It is shown that all of these mechanical tests can be reproduced accurately with a single set of constitutive parameters, the only difference between each fascicle being the distribution of their fibril crimp lengths. By accounting for fibril creep, we are able to predict how the fibril length distribution of a fascicle changes over time under a given deformation. Furthermore, the phenomenon of strain-dependent relaxation is explained as arising from the competition between the fibril and matrix relaxation functions.
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      A Recruitment Model of Tendon Viscoelasticity That Incorporates Fibril Creep and Explains Strain-Dependent Relaxation

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    contributor authorShearer, Tom
    contributor authorParnell, William J.
    contributor authorLynch, Barbara
    contributor authorScreen, Hazel R. C.
    contributor authorDavid Abrahams, I.
    date accessioned2022-02-04T14:15:59Z
    date available2022-02-04T14:15:59Z
    date copyright2020/02/24/
    date issued2020
    identifier issn0148-0731
    identifier otherbio_142_07_071003.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4273306
    description abstractSoft tissues exhibit complex viscoelastic behavior, including strain-rate dependence, hysteresis, and strain-dependent relaxation. In this paper, a model for soft tissue viscoelasticity is developed that captures all of these features and is based upon collagen recruitment, whereby fibrils contribute to tissue stiffness only when taut. We build upon existing recruitment models by additionally accounting for fibril creep and by explicitly modeling the contribution of the matrix to the overall tissue viscoelasticity. The fibrils and matrix are modeled as linear viscoelastic and each fibril has an associated critical strain (corresponding to its length) at which it becomes taut. The model is used to fit relaxation tests on three rat tail tendon fascicles and predict their response to cyclic loading. It is shown that all of these mechanical tests can be reproduced accurately with a single set of constitutive parameters, the only difference between each fascicle being the distribution of their fibril crimp lengths. By accounting for fibril creep, we are able to predict how the fibril length distribution of a fascicle changes over time under a given deformation. Furthermore, the phenomenon of strain-dependent relaxation is explained as arising from the competition between the fibril and matrix relaxation functions.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleA Recruitment Model of Tendon Viscoelasticity That Incorporates Fibril Creep and Explains Strain-Dependent Relaxation
    typeJournal Paper
    journal volume142
    journal issue7
    journal titleJournal of Biomechanical Engineering
    identifier doi10.1115/1.4045662
    page71003
    treeJournal of Biomechanical Engineering:;2020:;volume( 142 ):;issue: 007
    contenttypeFulltext
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