Please use this identifier to cite or link to this item: https://doi.org/10.1039/c0jm03234d
DC FieldValue
dc.titleHollow chitosan-silica nanospheres for doxorubicin delivery to cancer cells with enhanced antitumor effect in vivo
dc.contributor.authorYan, E.
dc.contributor.authorFu, Y.
dc.contributor.authorWang, X.
dc.contributor.authorDing, Y.
dc.contributor.authorQian, H.
dc.contributor.authorWang, C.-H.
dc.contributor.authorHu, Y.
dc.contributor.authorJiang, X.
dc.date.accessioned2014-06-17T07:42:29Z
dc.date.available2014-06-17T07:42:29Z
dc.date.issued2011-03-07
dc.identifier.citationYan, E., Fu, Y., Wang, X., Ding, Y., Qian, H., Wang, C.-H., Hu, Y., Jiang, X. (2011-03-07). Hollow chitosan-silica nanospheres for doxorubicin delivery to cancer cells with enhanced antitumor effect in vivo. Journal of Materials Chemistry 21 (9) : 3147-3155. ScholarBank@NUS Repository. https://doi.org/10.1039/c0jm03234d
dc.identifier.issn09599428
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/64034
dc.description.abstractHere we report the synthesis of hybrid hollow chitosan-silica nanospheres (CS-Silica NPs) with chitosan-polyacrylic acid (CS-PAA) nanoparticles as the template and doxorubicin (DOX) delivery based on CS-Silica NPs. The morphology and the microstructure of CS-Silica NPs were characterized by field emission scanning electron microscopy (FESEM) and X-ray photoelectron spectroscopy (XPS). The confocal laser scanning microscopy (CLSM) and flow cytometry experiments showed that the cellular uptake of the DOX-loaded CS-Silica NPs was time dependent. In addition, cellular internalization and intracellular distribution of DOX-loaded CS-Silica NPs indicated that the DOX was mainly distributed in the cell nucleus while the carriers were primarily located in the cytoplasm. In vivo antitumor response indicated that the DOX loaded CS-Silica hybrid hollow nanospheres exhibited superior antitumor effect over the free drug in vivo, which might be ascribable to the enhanced cellular uptake efficiency and the effective delivery of drug to the cell nucleus. © The Royal Society of Chemistry 2011.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c0jm03234d
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1039/c0jm03234d
dc.description.sourcetitleJournal of Materials Chemistry
dc.description.volume21
dc.description.issue9
dc.description.page3147-3155
dc.description.codenJMACE
dc.identifier.isiut000287369300051
Appears in Collections:Staff Publications

Show simple item record
Files in This Item:
There are no files associated with this item.

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.