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    A nanoparticulate system that enhances the efficacy of the tumoricide Dz13 when administered proximal to the lesion site

    Access Status
    Fulltext not available
    Authors
    Tan, M.
    Dunstan, D.
    Friedhuber, A.
    Choong, P.
    Dass, Crispin
    Date
    2010
    Type
    Journal Article
    
    Metadata
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    Citation
    Tan, M. and Dunstan, D. and Friedhuber, A. and Choong, P. and Dass, C. 2010. A nanoparticulate system that enhances the efficacy of the tumoricide Dz13 when administered proximal to the lesion site. Journal of Controlled Release. 144: pp. 196-202.
    Source Title
    Journal of Controlled Release
    DOI
    10.1016/j.jconrel.2010.01.011
    ISSN
    0168-3659
    URI
    http://hdl.handle.net/20.500.11937/18238
    Collection
    • Curtin Research Publications
    Abstract

    We demonstrate that Dz13, a DNA enzyme that cleaves c-Jun mRNA, and is capable of inhibiting cancer cell growth in vitro, can be encapsulated into chitosan nanoparticles. For optimisation of this chitosan-based formulation, pH 6, 0.02% chitosan concentration, and 55 °C were found to be best among the variables tested. Particles were 50-300. nm in diameter and encapsulated Dz13 was active when particles were exposed to cancer cells. Nanoparticles were stable during storage even for a month, but were not stable in mouse and human serum. In two different clinically-relevant disease models, and using a clinically-adoptable dosing regimen, these Dz13-nanoparticles were shown to be efficacious against a bone tumour (osteosarcoma), for which no real cure exists currently. However, no toxicity against other bone-dwelling cells was observed with the formulation, and no side-effects were noted in vivo in lymphatic and reticuloendothelial tissues proximal and distal to the administration site.

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