Copper-doped and copper-free bioactive glass nanopowders cytotoxicity and antibacterial activity assessment

Document Type : Research Note

Authors

1 Department of New Science and Technology Campus (Biomaterial Group), Semnan University, Semnan, P.O. Box 35131-19111, Iran

2 Department of Biomedical Engineering, Faculty of Engineering, University of Isfahan, Isfahan, P.O. Box 81746-13441, Iran

3 Biosensor Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

4 Department of Materials, Faculty of Engineering, Shahrekord University, Shahrekord, Iran

Abstract

The purpose of this study is to evaluate the antibacterial activity and cytotoxicity of copper-doped (Cu45SBG) and copper-free bioactive glass (45SBG) nanopowders. The antibacterial e ect was studied using Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) bacteria. The BG nanopowders were synthesized by the sol-gel
technique. They were characterized by various techniques and their cytotoxicity was evaluated by MTT assay. Chemical compositions of BGs were as the same as the predicted compositions. The size of the BGs with an amorphous structure was measured to be around 100 nm. Both BG nanopowders have no antibacterial e ect on broth concentrations less than 12.5 mg/ml. They demonstrated similar antibacterial activity on E. coli with
Minimum Bactericidal Concentration (MBC) of 12.5 mg/ml. Cu45SBG nanopowders with the MBC of 25 mg/ml were more ecient on S. aureous bacteria than 45SBG nanopowders with the MBC of 50 mg/ml. Compared to 45SBG, Cu45SBG showed much more cytotoxicity. 45SBG demonstrated similar cells viability to the control. It was concluded that to overcome cytotoxic e ect, Cu content of BGs nanopowders must be lower than the amount used in this research. Therefore, 45SBG nanopowders with considerable antibacterial activity could be used as a good candidate for biomedical applications.

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Scientia Iranica
Volume 24, Issue 3
Transactions on Nanotechnology (F)
May and June 2017
Pages 1706-1716

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History

  • Receive Date: 29 February 2016
  • Revise Date: 16 August 2016
  • Accept Date: 10 December 2016

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