Issue 46, 2014

Biocompatible graphene oxide as a folate receptor-targeting drug delivery system for the controlled release of anti-cancer drugs

Abstract

A novel graphene oxide (GO)-based nanocarrier has been designed for the targeting and pH-responsive controlled release of anti-cancer drugs via the classic amidation of the carboxyl groups of carboxylated graphene oxide (CG) with the amine end-groups of functional poly(ethylene glycol) (PEG) terminated with an amino group and a folic acid group (FA–PEG–NH2). The carboxylated graphene oxide conjugated folate-terminated poly(ethylene glycol) (CG–PEG–FA) nanocarrier containing 44.4 wt% of functional PEG brushes exhibits stable dispersibility in PBS media, outstanding cytocompatibility, high drug-loading capacity (0.3993 mg mg−1 for DOX) via π–π stacking interactions, perfect folate receptor-targeting and pH-activated controlled release properties, demonstrating that the nanocarrier could be a promising drug delivery system (DDS) for cancer therapy.

Graphical abstract: Biocompatible graphene oxide as a folate receptor-targeting drug delivery system for the controlled release of anti-cancer drugs

Associated articles

Supplementary files

Article information

Article type
Paper
Submitted
20 Mar 2014
Accepted
15 Apr 2014
First published
16 Apr 2014

RSC Adv., 2014,4, 24232-24239

Author version available

Biocompatible graphene oxide as a folate receptor-targeting drug delivery system for the controlled release of anti-cancer drugs

X. Zhao and P. Liu, RSC Adv., 2014, 4, 24232 DOI: 10.1039/C4RA02466D

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