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    Nonthermal Irreversible Electroporation for Tissue Decellularization

    Source: Journal of Biomechanical Engineering:;2010:;volume( 132 ):;issue: 009::page 91003
    Author:
    Mary Phillips
    ,
    Elad Maor
    ,
    Boris Rubinsky
    DOI: 10.1115/1.4001882
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Tissue scaffolding is a key component for tissue engineering, and the extracellular matrix (ECM) is nature’s ideal scaffold material. A conceptually different method is reported here for producing tissue scaffolds by decellularization of living tissues using nonthermal irreversible electroporation (NTIRE) pulsed electrical fields to cause nanoscale irreversible damage to the cell membrane in the targeted tissue while sparing the ECM and utilizing the body’s host response for decellularization. This study demonstrates that the method preserves the native tissue ECM and produces a scaffold that is functional and facilitates recellularization. A two-dimensional transient finite element solution of the Laplace and heat conduction equations was used to ensure that the electrical parameters used would not cause any thermal damage to the tissue scaffold. By performing NTIRE in vivo on the carotid artery, it is shown that in 3 days post NTIRE the immune system decellularizes the irreversible electroporated tissue and leaves behind a functional scaffold. In 7 days, there is evidence of endothelial regrowth, indicating that the artery scaffold maintained its function throughout the procedure and normal recellularization is taking place.
    keyword(s): Biological tissues , Electroporation , Tissue scaffolds , Carotid arteries , Electric fields AND Finite element analysis ,
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      Nonthermal Irreversible Electroporation for Tissue Decellularization

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    https://yetl.yabesh.ir/yetl1/handle/yetl/142547
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    contributor authorMary Phillips
    contributor authorElad Maor
    contributor authorBoris Rubinsky
    date accessioned2017-05-09T00:36:29Z
    date available2017-05-09T00:36:29Z
    date copyrightSeptember, 2010
    date issued2010
    identifier issn0148-0731
    identifier otherJBENDY-27166#091003_1.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/142547
    description abstractTissue scaffolding is a key component for tissue engineering, and the extracellular matrix (ECM) is nature’s ideal scaffold material. A conceptually different method is reported here for producing tissue scaffolds by decellularization of living tissues using nonthermal irreversible electroporation (NTIRE) pulsed electrical fields to cause nanoscale irreversible damage to the cell membrane in the targeted tissue while sparing the ECM and utilizing the body’s host response for decellularization. This study demonstrates that the method preserves the native tissue ECM and produces a scaffold that is functional and facilitates recellularization. A two-dimensional transient finite element solution of the Laplace and heat conduction equations was used to ensure that the electrical parameters used would not cause any thermal damage to the tissue scaffold. By performing NTIRE in vivo on the carotid artery, it is shown that in 3 days post NTIRE the immune system decellularizes the irreversible electroporated tissue and leaves behind a functional scaffold. In 7 days, there is evidence of endothelial regrowth, indicating that the artery scaffold maintained its function throughout the procedure and normal recellularization is taking place.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleNonthermal Irreversible Electroporation for Tissue Decellularization
    typeJournal Paper
    journal volume132
    journal issue9
    journal titleJournal of Biomechanical Engineering
    identifier doi10.1115/1.4001882
    journal fristpage91003
    identifier eissn1528-8951
    keywordsBiological tissues
    keywordsElectroporation
    keywordsTissue scaffolds
    keywordsCarotid arteries
    keywordsElectric fields AND Finite element analysis
    treeJournal of Biomechanical Engineering:;2010:;volume( 132 ):;issue: 009
    contenttypeFulltext
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