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    Synergistic Anticancer Effects Achieved by Co-Delivery of TRAIL and Paclitaxel Using Cationic Polymeric Micelles

    Access Status
    Fulltext not available
    Authors
    Lee, A.
    Wang, Y.
    Pervaiz, Shazib
    Fan, W.
    Yang, Y.
    Date
    2011
    Type
    Journal Article
    
    Metadata
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    Citation
    Lee, A. and Wang, Y. and Pervaiz, S. and Fan, W. and Yang, Y. 2011. Synergistic Anticancer Effects Achieved by Co-Delivery of TRAIL and Paclitaxel Using Cationic Polymeric Micelles. Macromolecular Bioscience. 11 (2): pp. 296-307.
    Source Title
    Macromolecular Bioscience
    DOI
    10.1002/mabi.201000332
    ISSN
    1616-5187
    School
    School of Biomedical Sciences
    URI
    http://hdl.handle.net/20.500.11937/51227
    Collection
    • Curtin Research Publications
    Abstract

    Cationic micellar nanoparticles self-assembled from a biodegradable amphiphilic copolymer have been used to deliver human TRAIL and paclitaxel simultaneously. Polyplexes formed between paclitaxel-loaded nanoparticles and TRAIL are stable with a size of ˜180nm and a zeta potential at ˜75mV. Anticancer effects and apoptotic pathway mechanisms of this drug-and-protein co-delivery system are investigated in various human breast cancer cell lines with different TRAIL sensitivity. The co-delivery nanoparticulate system induces synergistic anti-cancer activities with limited toxicity in non-cancerous cells. An advantage of this co-delivery is a significantly higher anti-cancer effect as compared to free drug and protein formulations. In this study, cationic polymeric micelles have been used to deliver human TRAIL and paclitaxel simultaneously into various human breast cancer cell lines. The co-delivery achieves synergistic anti-cancer activities with limited toxicity in non-cancerous cells. This system also induces significantly higher anti-cancer effects as compared to free drug and protein formulations. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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