• Title of article

    Cyclic RGD-modified chitosan/graphene oxide polymers for drug delivery and cellular imaging

  • Author/Authors

    Wang، نويسنده , , Chen and Chen، نويسنده , , Binbin and Zou، نويسنده , , Meijuan and Cheng، نويسنده , , Gang، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2014
  • Pages
    9
  • From page
    332
  • To page
    340
  • Abstract
    Polymers based on cyclic RGD-modified chitosan/graphene oxide are investigated in this paper as an innovative type of drug delivery system for hepatocellular carcinoma-targeted therapy and imaging. The system was prepared using a simple noncovalent method by coating drug-loaded graphene oxide (GO) with cyclic RGD-modified chitosan (RC). The results show that an efficient loading of doxorubicin (DOX) on GO (1.00 mg/mg) was obtained. The system exhibits a pH-responsive behavior because of the hydrogen bonding interaction between GO and RC, and may be very stable under physiological conditions but with release at a lower pH (tumor environment). In addition, cellular uptake and proliferation studies using hepatoma cells (Bel-7402, SMMC-7721, HepG2) indicated that the cRGD-modified chitosan/graphene oxide polymer could recognize hepatoma cells and promote drug uptake by the cells, especially for cells overexpressing integrins. Together, these results demonstrate that the RC/GO polymers provide a multifunctional drug delivery system with the ability to target hepatocarcinoma cells, and are pH-responsive and can be efficiently loaded with a number of therapeutic agents for biomedical applications.
  • Keywords
    Cyclic RGD , Graphene oxide , PH-RESPONSIVE , Controlled release , Hepatoma cells targeting
  • Journal title
    Colloids and Surfaces B Biointerfaces
  • Serial Year
    2014
  • Journal title
    Colloids and Surfaces B Biointerfaces
  • Record number

    1978881