| Literature DB >> 28254282 |
Poornima Agrawal1, Rahul Pratap Singh1, Laksmi Kumari2, Gunjan Sharma3, Biplob Koch4, Chellapa V Rajesh5, Abhishesh K Mehata2, Sanjay Singh2, Bajarangprasad L Pandey1, Madaswamy S Muthu6.
Abstract
Brain 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.Entities:
Keywords: Brain cancer; Chitosan; Synergistic effect; TPGS; Targeted nanomedicines; Transferrin receptor
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Year: 2017 PMID: 28254282 DOI: 10.1016/j.msec.2017.02.008
Source DB: PubMed Journal: Mater Sci Eng C Mater Biol Appl ISSN: 0928-4931 Impact factor: 7.328