Fabrication an Antibacterial Surface on Composite Porous Scaffold

Article Preview

Abstract:

Elimination of the residual microorganisms from an infectious bone defects and the prevention of subsequent re-infection are of importance for chronic osteomyelitis treatment. The application of bone repair materials with antibacterial properties in such a condition has advantages. The present study reported a novel method to fabricate nanohydroxyapatite/polyurethane (n-HA/PU) based antibacterial porous scaffolds through immobilization "core-shell" silver-based mesoporous silica particles (Ag@SiO2), i.e., silver nanoparticle as core and mesoporous silica as shell, on the surface of n-HA/PU scaffold. The samples were characterized by Scanning Electron Microscope (SEM) and antibacterial tests. The results revealed that the Ag@SiO2 nanoparticles distributed uniformly on the surface of n-HA/PU porous scaffold. The Ag@SiO2 could been kept on the surface of n-HA/PU porous scaffold more than 2 weeks, resulting in long-lasting the release of silver ions and antibacterial ability. The porous n-HA/PU scaffolds with an antibacterial surface may hold promise to be used in infectious bone defects repair.

You might also be interested in these eBooks

Info:

Periodical:

Pages:

291-294

Citation:

Online since:

March 2015

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2015 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

* - Corresponding Author

[1] A.G. Gristina, Science. Vol. 237 (1987), p.1588.

Google Scholar

[2] P. Stoodley, S. Kathju, F.Z. Hu, G. Erdos, J.E. Levenson, N. Mehta, B. Dice, S. Johnson, L. Hall-Stoodley and L. Nistico, Clin Orthop Relat Res. Vol. 437(2005), p.31.

DOI: 10.1097/01.blo.0000175129.83084.d5

Google Scholar

[3] Y. TABATA, Necessity of drug delivery systems to tissue engineering, in Biomaterials and Drug Delivery Toward the New Millennium, edited by K. D. Park (Han Rim Won Publisher, Seoul, Korea, 2000).

Google Scholar

[4] D. Huang, Y. Zuo, Q. Zou, L. Zhang, J.D. Li, L. Cheng, J. Shen and Y.B. Li, J. Biomater. Sci. Polym. Ed. Vol. 22(2011), p.931.

Google Scholar

[5] J.E. Gray, P.R. Norton, R. Alnouno, C.L. Marolda, M.A. Valvano and K. Griffiths, Biomaterials. Vol. 24(2003), p.2759.

DOI: 10.1016/s0142-9612(03)00057-7

Google Scholar

[6] H. Yang, Y. Liu, Q.H. Shen, L.F. Chen, W.H. You, X.M. Wang and J.S. Sheng, J. Mater. Chem. Vol. 22(2012), p.24132.

Google Scholar

[7] L. Wang, Y.B. Li, Y. Zuo, L. Zhang, Q. Zou, L. Cheng and H. Jiang, Biomed. Mater. Vol. 4 (2009).

Google Scholar

[8] L.M. Li, Y. Zuo, J.J. Du, J.D. Li, B. Sun and Y.B. Li, J. Inorg. Mater. Vol. 28(2013), p.811.

Google Scholar

[9] H.H. Liu, L. Zhang, P.J. Shi, L. Wang, D. Huang, J. Shen, P.J. Shi and Y.B. Li, J. Biomed. Mater. Res B. Vol. 95B(2010), p.36.

Google Scholar