A nanoparticulate system that enhances the efficacy of the tumoricide Dz13 when administered proximal to the lesion site
dc.contributor.author | Tan, M. | |
dc.contributor.author | Dunstan, D. | |
dc.contributor.author | Friedhuber, A. | |
dc.contributor.author | Choong, P. | |
dc.contributor.author | Dass, Crispin | |
dc.date.accessioned | 2017-01-30T12:06:36Z | |
dc.date.available | 2017-01-30T12:06:36Z | |
dc.date.created | 2014-09-02T20:01:14Z | |
dc.date.issued | 2010 | |
dc.identifier.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. | |
dc.identifier.uri | http://hdl.handle.net/20.500.11937/18238 | |
dc.identifier.doi | 10.1016/j.jconrel.2010.01.011 | |
dc.description.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. | |
dc.publisher | Elsevier | |
dc.title | A nanoparticulate system that enhances the efficacy of the tumoricide Dz13 when administered proximal to the lesion site | |
dc.type | Journal Article | |
dcterms.source.volume | 144 | |
dcterms.source.startPage | 196 | |
dcterms.source.endPage | 202 | |
dcterms.source.issn | 0168-3659 | |
dcterms.source.title | Journal of Controlled Release | |
curtin.accessStatus | Fulltext not available |