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    Characterization of Cell Constructs Generated With Inkjet Printing Technology Using In Vivo Magnetic Resonance Imaging

    Source: Journal of Manufacturing Science and Engineering:;2008:;volume( 130 ):;issue: 002::page 21013
    Author:
    Tao Xu
    ,
    John Olson
    ,
    Weixin Zhao
    ,
    Jian-Ming Zhu
    ,
    James J. Yoo
    ,
    Anthony Atala
    DOI: 10.1115/1.2902857
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: We report the use of a high resolution magnetic resonance (MR) imaging technique to monitor the development and maturation of tissue-printed constructs in vivo. Layer-by-layer inkjet printing technology was used to fabricate three different tissue constructs on alginate∕collagen gels: bovine aortic endothelial cell-printed (to represent soft tissue), human amniotic fluid-derived stem cell-printed (to represent hard tissue as they underwent osteogenic differentiation in vivo), and cell-free constructs (scaffold only). The constructs were subcutaneously implanted into athymic mice and regularly monitored using a 7T magnetic resonance imaging (MRI) scanner. The three tissue construct types showed distinct image contrast characteristics due to the different tissue microstructures and biochemical compositions at various time points. In addition, changes in tissue microvasculature were examined with dynamic perfusion MRI. These results indicate that high resolution MRI is a promising method for noninvasive, long-term monitoring of the status of cell-printed construct growth, differentiation, and vascularization.
    keyword(s): Biological tissues , Magnetic resonance imaging , Printing AND Imaging ,
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      Characterization of Cell Constructs Generated With Inkjet Printing Technology Using In Vivo Magnetic Resonance Imaging

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    http://yetl.yabesh.ir/yetl1/handle/yetl/138757
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    contributor authorTao Xu
    contributor authorJohn Olson
    contributor authorWeixin Zhao
    contributor authorJian-Ming Zhu
    contributor authorJames J. Yoo
    contributor authorAnthony Atala
    date accessioned2017-05-09T00:29:28Z
    date available2017-05-09T00:29:28Z
    date copyrightApril, 2008
    date issued2008
    identifier issn1087-1357
    identifier otherJMSEFK-28027#021013_1.pdf
    identifier urihttp://yetl.yabesh.ir/yetl/handle/yetl/138757
    description abstractWe report the use of a high resolution magnetic resonance (MR) imaging technique to monitor the development and maturation of tissue-printed constructs in vivo. Layer-by-layer inkjet printing technology was used to fabricate three different tissue constructs on alginate∕collagen gels: bovine aortic endothelial cell-printed (to represent soft tissue), human amniotic fluid-derived stem cell-printed (to represent hard tissue as they underwent osteogenic differentiation in vivo), and cell-free constructs (scaffold only). The constructs were subcutaneously implanted into athymic mice and regularly monitored using a 7T magnetic resonance imaging (MRI) scanner. The three tissue construct types showed distinct image contrast characteristics due to the different tissue microstructures and biochemical compositions at various time points. In addition, changes in tissue microvasculature were examined with dynamic perfusion MRI. These results indicate that high resolution MRI is a promising method for noninvasive, long-term monitoring of the status of cell-printed construct growth, differentiation, and vascularization.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleCharacterization of Cell Constructs Generated With Inkjet Printing Technology Using In Vivo Magnetic Resonance Imaging
    typeJournal Paper
    journal volume130
    journal issue2
    journal titleJournal of Manufacturing Science and Engineering
    identifier doi10.1115/1.2902857
    journal fristpage21013
    identifier eissn1528-8935
    keywordsBiological tissues
    keywordsMagnetic resonance imaging
    keywordsPrinting AND Imaging
    treeJournal of Manufacturing Science and Engineering:;2008:;volume( 130 ):;issue: 002
    contenttypeFulltext
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    DSpace software copyright © 2002-2015  DuraSpace
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