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|dc.title||Chitosan-functionalized graphene oxide as a nanocarrier for drug and gene delivery|
|dc.identifier.citation||Bao, H., Pan, Y., Ping, Y., Sahoo, N.G., Wu, T., Li, L., Li, J., Gan, L.H. (2011-06-06). Chitosan-functionalized graphene oxide as a nanocarrier for drug and gene delivery. Small 7 (11) : 1569-1578. ScholarBank@NUS Repository. https://doi.org/10.1002/smll.201100191|
|dc.description.abstract||The covalent functionalization of graphene oxide (GO) with chitosan (CS) is successfully accomplished via a facile amidation process. The CS-grafted GO (GO-CS) sheets consist of about 64 wt.% CS, which imparts them with a good aqueous solubility and biocompatibility. Additionally, the physicochemical properties of GO-CS are studied. As a novel nanocarrier, GO-CS is applied to load a water-insoluble anticancer drug, camptothecin (CPT), via π-π stacking and hydrophobic interactions. It is demonstrated that GO-CS possesses a superior loading capacity for CPT, and the GO-CS-CPT complexes show remarkably high cytotoxicity in HepG2 and HeLa cell lines compared to the pure drug. At the same time, GO-CS is also able to condense plasmid DNA into stable, nanosized complexes, and the resulting GO-CS/pDNA nanoparticles exhibit reasonable transfection efficiency in HeLa cells at certain nitrogen/phosphate ratios. Therefore, the GO-CS nanocarrier is able to load and deliver both anticancer drugs and genes. The covalent functionalization of graphene oxide (GO) with chitosan (CS) is accomplished via a facile method. It is demonstrated that GO-CS possesses a superior loading capacity for camptothecin (CPT), and the GO-CS-CPT complexes show remarkably high cytotoxicity in cancer cells. In addition, GO-CS is able to transport plasmid DNA into HeLa cells with a reasonable transfection efficiency. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.|
|Appears in Collections:||Staff Publications|
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