4.7 Article

Fe3O4@PEG-coated dendrimer modified graphene oxide nanocomposite as a pH-sensitive drug carrier for targeted delivery of doxorubicin

Journal

JOURNAL OF ALLOYS AND COMPOUNDS
Volume 879, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jallcom.2021.160426

Keywords

Magnetic nanoparticles; Polyethylene glycol; Doxorubicin; Graphene oxide; Triazine dendrimer

Funding

  1. University of Tabriz [968645105]
  2. Research Center for Pharmaceutical Nanotechnology (RCPN), Tabriz University of Medical Science

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The study successfully fabricated a triazine dendrimer-functionalized graphene oxide nanocarrier for drug delivery systems with potential applications in cancer treatment. The results showed that the nanocarrier exhibited pH-responsive drug release behavior, excellent biocompatibility, and higher apoptotic effects on breast cancer cells.
Since dendrimer-based magnetic nanoparticles have presented remarkable potential as carriers in biomedical applications, it is worthwhile to construct a dendrimer-based drug delivery system for cancer treatment. Hence, in the present study, triazine dendrimer functionalized graphene oxide (GO-DT G2.5) was successfully fabricated by the divergent method. Then, the Fe3O4@PEG nanoparticles were attached to the surface of GO-TD G2.5 (GO-TD-Fe3O4@PEG) as a new magnetic nanocarrier for effective loading and the pH-responsive release of Doxorubicin (DOX). The structure and morphology of the synthesized GO-TD-Fe3O4@PEG were characterized by BET, XRD, DLS/ Zeta potential, UV-vis, FT-IR, AFM, SEM, and VSM analysis. The surface morphology indicated that the average thickness of the sheets in the synthesized nanocarrier had approximately 144.21 nm. The encapsulation efficiency (EE) and drug-loading content (DLC) of this system were obtained similar to 92.6 and similar to 9.26%, respectively. The in vitro release studies of DOX from GO-TD-Fe3O4@PEG were performed at various pH values and found that the release process was noticeably controlled pHresponsive behavior. In vitro cytotoxicity studies of the as-synthesized GO-TD-Fe3O4@PEG against normal cell line (MCF-10A) and breast cancer cell line (MCF-7) confirmed that the non-toxic GO-TD-Fe3O4@PEG has excellent biocompatibility. DAPI staining and apoptosis analysis by flow-cytometry demonstrated that the apoptotic effects of GO-TD-Fe3O4@PEG-DOX have higher in comparison to free DOX. Cellular uptake also showed a high uptake percentage for GO-TD-Fe3O4@PEG-DOX than free DOX within 4 h. Therefore, the obtained results in this work suggesting that GO-TD-Fe3O4@PEG nanocomposite is a promising nanocarrier for targeted delivery and controlled release of anticancer drugs for biomedical applications. (C) 2021 Published by Elsevier B.V.

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