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    Novel pH-responsive dextrin nanogels for doxorubicin delivery to cancer cells with reduced cytotoxicity to cardiomyocytes and stem cells

    Access Status
    Fulltext not available
    Authors
    Manchun, S.
    Cheewatanakornkool, K.
    Dass, Crispin
    Sriamornsak, P.
    Date
    2014
    Type
    Journal Article
    
    Metadata
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    Citation
    Manchun, S. and Cheewatanakornkool, K. and Dass, C. and Sriamornsak, P. 2014. Novel pH-responsive dextrin nanogels for doxorubicin delivery to cancer cells with reduced cytotoxicity to cardiomyocytes and stem cells. Carbohydrate Polymers. 114: pp. 78-86.
    Source Title
    Carbohydrate Polymers
    DOI
    10.1016/j.carbpol.2014.08.002
    ISSN
    0144-8617
    School
    School of Pharmacy
    URI
    http://hdl.handle.net/20.500.11937/7733
    Collection
    • Curtin Research Publications
    Abstract

    The aim of this study was to develop pH-responsive dextrin nanogels (DNGs) capable of triggered intracellular DOX release at the lower pH of cancer cells. DNGs were prepared by an emulsion cross-linking method using glyoxal as cross-linker to create an acid-labile bond. A higher molecular weight of dextrin with increasing mole ratio of dextrin to glyoxal decreased the average diameter of DNGs. DNGs showed slightly negative surface charge and pH-responsive behavior. The in vitro drug release was slow at pH 7.4 and increased with decreasing pH (pH 5 > 6.8). The cytotoxicity of DOX-loaded DNGs in mesenchymal stem cells and cardiomyocytes was lower than that of free DOX. Moreover, DOX-loaded DNGs were efficiently internalized by tumor cells with rapid release of DOX into the nucleus. Thus, DOX-loaded DNGs were successful for intracellular targeted anti-tumor drug delivery and reducing side-effects to non-tumor cells such as cardiomyocytes and stem cells.

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