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    Motion of Red Blood Cells in Capillaries With Variable Cross-Sections

    Source: Journal of Biomechanical Engineering:;1996:;volume( 118 ):;issue: 004::page 538
    Author:
    T. W. Secomb
    ,
    R. Hsu
    DOI: 10.1115/1.2796041
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Red blood cells undergo continual deformation when traversing microvessels in living tissues. This may contribute to higher resistance to blood flow observed in living microvessels, compared with that in corresponding uniform glass tubes. We use a theoretical model to simulate single-file motion of red cells though capillaries with variable cross-sections, assuming axisymmetric geometry. Effects of cell membrane shear viscosity and elasticity are included, but bending resistance is neglected. Lubrication theory is used to describe the flow of surrounding plasma. When a red cell encounters a region of capillary narrowing, additional energy is dissipated, due to membrane viscosity, and due to narrowing of the lubrication layer, increasing the flow resistance. Predicted resistance to cell motion in a vessel with periodic constrictions (diameter varying between 5 μm and 4 μm) is roughly twice that in a uniform vessel with diameter 4.5 μm. Effects of transient red cell deformations may contribute significantly to blood flow resistance in living microvessels.
    keyword(s): Motion , Cross section (Physics) , Erythrocytes , Electrical resistance , Viscosity , Flow (Dynamics) , Deformation , Blood flow , Membranes , Vessels , Lubrication theory , Shear (Mechanics) , Biological tissues , Geometry , Lubrication , Glass , Elasticity AND Plasmas (Ionized gases) ,
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      Motion of Red Blood Cells in Capillaries With Variable Cross-Sections

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    http://yetl.yabesh.ir/yetl1/handle/yetl/116539
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    contributor authorT. W. Secomb
    contributor authorR. Hsu
    date accessioned2017-05-08T23:49:23Z
    date available2017-05-08T23:49:23Z
    date copyrightNovember, 1996
    date issued1996
    identifier issn0148-0731
    identifier otherJBENDY-25968#538_1.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/116539
    description abstractRed blood cells undergo continual deformation when traversing microvessels in living tissues. This may contribute to higher resistance to blood flow observed in living microvessels, compared with that in corresponding uniform glass tubes. We use a theoretical model to simulate single-file motion of red cells though capillaries with variable cross-sections, assuming axisymmetric geometry. Effects of cell membrane shear viscosity and elasticity are included, but bending resistance is neglected. Lubrication theory is used to describe the flow of surrounding plasma. When a red cell encounters a region of capillary narrowing, additional energy is dissipated, due to membrane viscosity, and due to narrowing of the lubrication layer, increasing the flow resistance. Predicted resistance to cell motion in a vessel with periodic constrictions (diameter varying between 5 μm and 4 μm) is roughly twice that in a uniform vessel with diameter 4.5 μm. Effects of transient red cell deformations may contribute significantly to blood flow resistance in living microvessels.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleMotion of Red Blood Cells in Capillaries With Variable Cross-Sections
    typeJournal Paper
    journal volume118
    journal issue4
    journal titleJournal of Biomechanical Engineering
    identifier doi10.1115/1.2796041
    journal fristpage538
    journal lastpage544
    identifier eissn1528-8951
    keywordsMotion
    keywordsCross section (Physics)
    keywordsErythrocytes
    keywordsElectrical resistance
    keywordsViscosity
    keywordsFlow (Dynamics)
    keywordsDeformation
    keywordsBlood flow
    keywordsMembranes
    keywordsVessels
    keywordsLubrication theory
    keywordsShear (Mechanics)
    keywordsBiological tissues
    keywordsGeometry
    keywordsLubrication
    keywordsGlass
    keywordsElasticity AND Plasmas (Ionized gases)
    treeJournal of Biomechanical Engineering:;1996:;volume( 118 ):;issue: 004
    contenttypeFulltext
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