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    Smart pH-responsive nanocarriers based on nano-graphene oxide for combined chemo- and photothermal therapy overcoming drug resistance

    Access Status
    Fulltext not available
    Authors
    Feng, L.
    Li, K.
    Shi, X.
    Gao, M.
    Liu, Jian
    Liu, Z.
    Date
    2014
    Type
    Journal Article
    
    Metadata
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    Citation
    Feng, L. and Li, K. and Shi, X. and Gao, M. and Liu, J. and Liu, Z. 2014. Smart pH-responsive nanocarriers based on nano-graphene oxide for combined chemo- and photothermal therapy overcoming drug resistance. Advanced Healthcare Materials. 3 (8): pp. 1261-1271.
    Source Title
    Advanced Healthcare Materials
    DOI
    10.1002/adhm.201300549
    ISSN
    2192-2640
    School
    WASM: Minerals, Energy and Chemical Engineering (WASM-MECE)
    URI
    http://hdl.handle.net/20.500.11937/72489
    Collection
    • Curtin Research Publications
    Abstract

    A pH-responsive nanocarrier is developed by coating nanoscale graphene oxide (NGO) with dual types of polymers, polyethylene glycol (PEG) and poly(allylamine hydrochloride) (PAH), the latter of which is then modified with 2,3-dimethylmaleic anhydride (DA) to acquire pH-dependent charge reversibility. After loading with doxorubicin (DOX), a chemotherapy drug, the obtained NGO-PEG-DA/DOX complex exhibits a dual pH-responsiveness, showing markedly enhanced cellular uptake under the tumor microenvironmental pH, and accelerated DOX release under a further lowered pH inside cell lysosomes. Combining such a unique behavior with subsequently slow efflux of DOX, NGO-PEG-DA/DOX offers remarkably improved cell killing for drug-resistant cancer cells under the tumor microenvironmental pH in comparison with free DOX. Exploiting its excellent photothermal conversion ability, combined chemo- and photothermal therapy is further demonstrated using NGO-PEG-DA/DOX, realizing a synergistic therapeutic effect. This work presents a novel design of surface chemistry on NGO for the development of smart drug delivery systems responding to the tumor microenvironment and external physical stimulus, with the potential to overcome drug resistance. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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