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

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 th...

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Main Authors: Tan, M., Dunstan, D., Friedhuber, A., Choong, P., Dass, Crispin
Format: Journal Article
Published: Elsevier 2010
Online Access:http://hdl.handle.net/20.500.11937/18238
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author Tan, M.
Dunstan, D.
Friedhuber, A.
Choong, P.
Dass, Crispin
author_facet Tan, M.
Dunstan, D.
Friedhuber, A.
Choong, P.
Dass, Crispin
author_sort Tan, M.
building Curtin Institutional Repository
collection Online Access
description 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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spelling curtin-20.500.11937-182382017-09-13T13:43:52Z A nanoparticulate system that enhances the efficacy of the tumoricide Dz13 when administered proximal to the lesion site Tan, M. Dunstan, D. Friedhuber, A. Choong, P. Dass, Crispin 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. 2010 Journal Article http://hdl.handle.net/20.500.11937/18238 10.1016/j.jconrel.2010.01.011 Elsevier restricted
spellingShingle Tan, M.
Dunstan, D.
Friedhuber, A.
Choong, P.
Dass, Crispin
A nanoparticulate system that enhances the efficacy of the tumoricide Dz13 when administered proximal to the lesion site
title A nanoparticulate system that enhances the efficacy of the tumoricide Dz13 when administered proximal to the lesion site
title_full A nanoparticulate system that enhances the efficacy of the tumoricide Dz13 when administered proximal to the lesion site
title_fullStr A nanoparticulate system that enhances the efficacy of the tumoricide Dz13 when administered proximal to the lesion site
title_full_unstemmed A nanoparticulate system that enhances the efficacy of the tumoricide Dz13 when administered proximal to the lesion site
title_short A nanoparticulate system that enhances the efficacy of the tumoricide Dz13 when administered proximal to the lesion site
title_sort nanoparticulate system that enhances the efficacy of the tumoricide dz13 when administered proximal to the lesion site
url http://hdl.handle.net/20.500.11937/18238