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TPGS-chitosan cross-linked targeted nanoparticles for effective brain cancer therapy

dc.contributor.authorAgrawal P.; Singh R.P.; Sonali; Kumari L.; Sharma G.; Koch B.; Rajesh C.V.; Mehata A.K.; Singh S.; Pandey B.L.; Muthu M.S.
dc.date.accessioned2025-05-24T09:29:59Z
dc.description.abstractBrain cancer, up-regulated with transferrin receptor led to concept of transferrin receptor targeted anticancer therapeutics. Docetaxel loaded D-α-tocopherol polyethylene glycol 1000 succinate conjugated chitosan (TPGS-chitosan) nanoparticles were prepared with or without transferrin decoration. In vitro experiments using C6 glioma cells showed that docetaxel loaded chitosan nanoparticles, non-targeted and transferrin receptor targeted TPGS-chitosan nanoparticles have enhanced the cellular uptake and cytotoxicity. The IC50 values of non-targeted and transferrin receptor targeted nanoparticles from cytotoxic assay were found to be 27 and 148 folds, respectively higher than Docel™. In vivo pharmacokinetic study showed 3.23 and 4.10 folds enhancement in relative bioavailability of docetaxel for non-targeted and transferrin receptor targeted nanoparticles, respectively than Docel™. The results have demonstrated that transferrin receptor targeted nanoparticles could enhance the cellular internalization and cytotoxicity of docetaxel via transferrin receptor with improved pharmacokinetics for clinical applications. © 2017 Elsevier B.V.
dc.identifier.doihttps://doi.org/10.1016/j.msec.2017.02.008
dc.identifier.urihttp://172.23.0.11:4000/handle/123456789/16532
dc.relation.ispartofseriesMaterials Science and Engineering C
dc.titleTPGS-chitosan cross-linked targeted nanoparticles for effective brain cancer therapy

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