Graphene oxide nanoribbons as nanomaterial for bone regeneration: Effects on cytotoxicity, gene expression and bactericidal effect.

Mater Sci Eng C Mater Biol Appl

Laboratory of Biomedical Nanotechnology, Research and Development Institute, University of Vale do Paraiba, Av. Shishima Hifumi, 2911, CEP: 12244-000 São José dos Campos, SP, Brazil; Laboratory of Biomedical Nanotechnology, Universidade Brasil, Rua Carolina Fonseca 235, 08230-030 São Paulo, Brazil; Biomaterials Innovation Research Center, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Cambridge, MA 02139, USA; Department of Chemical Engineering, Northeastern University, Boston, MA 02115, USA. Electronic address:

Published: September 2017

Graphene oxide nanoribbons (O-GNR) surges as an interesting nanomaterial for biomedical applications due to feasibility to incorporate functional groups and possible bactericidal properties. Herein, high concentrations of O-GNR were biologically evaluated using human osteoblast cells and gram positive and negative bacteria. Briefly, our goal were to evaluate: (1) synthetic pathway, (2) characterization and (3) effects of O-GNR composition and structural factors as a new approach for biomedical applications. For this, O-GNR were produced combining chemical vapor deposition and oxygen plasma treatment of multiwalled carbon nanotubes. Then, we analyzed the bioactivity, cell viability, osteogenic differentiation, matrix mineralization, mRNA levels of the five genes related direct to bone repair and bactericidal effect of high concentrations of O-GNR (10μgmL, 100μgmL, 200μgmL and 300μgmL). Impressively, O-GNR showed no cytotoxic effects up to a concentration of 100μgmL and no gene expression alteration when used in its dose. We also observed that S. aureus and E. coli bacteria are susceptible to damage when incubated with 100μgmL of O-GNR, showing approximately 50% of bacterial death. We consider that O-GNR displays attractive properties when used at a suitable dose, displaying bactericidal effect and apparently lacking to cause damages in the bone repair process.

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http://dx.doi.org/10.1016/j.msec.2017.03.278DOI Listing

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