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    A Steady-State Mass Transfer Model of Removing CPAs From Cryopreserved Blood With Hollow Fiber Modules

    Source: Journal of Biomechanical Engineering:;2010:;volume( 132 ):;issue: 001::page 11002
    Author:
    Weiping Ding
    ,
    Shelly Heimfeld
    ,
    Jo-Anna Reems
    ,
    Dayong Gao
    ,
    Xiaoming Zhou
    DOI: 10.1115/1.4000110
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Hollow fiber modules are commonly used to conveniently and efficiently remove cryoprotective agents (CPAs) from cryopreserved cell suspensions. In this paper, a steady-state model coupling mass transfers across cell and hollow fiber membranes is theoretically developed to evaluate the removal of CPAs from cryopreserved blood using hollow fiber modules. This steady-state model complements the unsteady-state model, which was presented in our previous study. The steady-state model, unlike the unsteady-state model, can be used to evaluate the effect of ultrafiltration flow rates on the clearance of CPAs. The steady-state model is validated by experimental results, and then is compared with the unsteady-state model. Using the steady-state model, the effects of ultrafiltration flow rates, NaCl concentrations in dialysate, blood flow rates and dialysate flow rates on CPA concentration variation and cell volume response are investigated in detail. According to the simulative results, the osmotic damage of red blood cells can easily be reduced by increasing ultrafiltration flow rates, increasing NaCl concentrations in dialysate, increasing blood flow rates, or decreasing dialysate flow rates.
    keyword(s): Flow (Dynamics) , Mass transfer , Fibers , Blood , Membranes AND Steady state ,
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      A Steady-State Mass Transfer Model of Removing CPAs From Cryopreserved Blood With Hollow Fiber Modules

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    http://yetl.yabesh.ir/yetl1/handle/yetl/142681
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    contributor authorWeiping Ding
    contributor authorShelly Heimfeld
    contributor authorJo-Anna Reems
    contributor authorDayong Gao
    contributor authorXiaoming Zhou
    date accessioned2017-05-09T00:36:43Z
    date available2017-05-09T00:36:43Z
    date copyrightJanuary, 2010
    date issued2010
    identifier issn0148-0731
    identifier otherJBENDY-27091#011002_1.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/142681
    description abstractHollow fiber modules are commonly used to conveniently and efficiently remove cryoprotective agents (CPAs) from cryopreserved cell suspensions. In this paper, a steady-state model coupling mass transfers across cell and hollow fiber membranes is theoretically developed to evaluate the removal of CPAs from cryopreserved blood using hollow fiber modules. This steady-state model complements the unsteady-state model, which was presented in our previous study. The steady-state model, unlike the unsteady-state model, can be used to evaluate the effect of ultrafiltration flow rates on the clearance of CPAs. The steady-state model is validated by experimental results, and then is compared with the unsteady-state model. Using the steady-state model, the effects of ultrafiltration flow rates, NaCl concentrations in dialysate, blood flow rates and dialysate flow rates on CPA concentration variation and cell volume response are investigated in detail. According to the simulative results, the osmotic damage of red blood cells can easily be reduced by increasing ultrafiltration flow rates, increasing NaCl concentrations in dialysate, increasing blood flow rates, or decreasing dialysate flow rates.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleA Steady-State Mass Transfer Model of Removing CPAs From Cryopreserved Blood With Hollow Fiber Modules
    typeJournal Paper
    journal volume132
    journal issue1
    journal titleJournal of Biomechanical Engineering
    identifier doi10.1115/1.4000110
    journal fristpage11002
    identifier eissn1528-8951
    keywordsFlow (Dynamics)
    keywordsMass transfer
    keywordsFibers
    keywordsBlood
    keywordsMembranes AND Steady state
    treeJournal of Biomechanical Engineering:;2010:;volume( 132 ):;issue: 001
    contenttypeFulltext
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