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dc.contributor.authorLee, A.
dc.contributor.authorWang, Y.
dc.contributor.authorPervaiz, Shazib
dc.contributor.authorFan, W.
dc.contributor.authorYang, Y.
dc.date.accessioned2017-03-17T08:30:03Z
dc.date.available2017-03-17T08:30:03Z
dc.date.created2017-02-19T19:31:45Z
dc.date.issued2011
dc.identifier.citationLee, 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.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/51227
dc.identifier.doi10.1002/mabi.201000332
dc.description.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.

dc.titleSynergistic Anticancer Effects Achieved by Co-Delivery of TRAIL and Paclitaxel Using Cationic Polymeric Micelles
dc.typeJournal Article
dcterms.source.volume11
dcterms.source.number2
dcterms.source.startPage296
dcterms.source.endPage307
dcterms.source.issn1616-5187
dcterms.source.titleMacromolecular Bioscience
curtin.departmentSchool of Biomedical Sciences
curtin.accessStatusFulltext not available


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