Issue 5, 2015

Antibacterial and osteoinductive capability of orthopedic materials via cation–π interaction mediated positive charge

Abstract

Both implant centered infection and deficient osteoinduction are pivotal issues for orthopedic implants in early and long-term osseointegration, but constructing a functional bio-interface that can overcome these two problems is highly challenging. Our study reveals that a bio-interface with promoted positive charges plays an active role in simultaneously enhancing the antibacterial and osteoinductive capability of orthopedic implants. The positively charged bio-interface is fabricated by a simple dipping method, in which the cationic polymer (polyhexamethylene biguanidine, PHMB) is immobilized in the conjugated polydopamine coating. Mediated by the cation–π interaction, the immobilized PHMB elevates the surface potential resulting in excellent antibacterial efficacy corresponding to 5 ppm of free PHMB. The materials exhibit far better cytocompatibility than free PHMB at the dose which kills over 50% of the cells. Most importantly, the cationic surface can function as a bioelectrical microenvironment to guide bone mesenchymal stem cells and consequently, enhanced cellular viability and proliferation together with upregulated osteogenesis are achieved. The cation–π interaction mediated cationic surface overcomes the disadvantages plaguing the immobilized cationic antibacterial compounds prepared by other methods and is applicable to different types of biomedical materials requiring antibacterial and osteoinductive bio-interfaces.

Graphical abstract: Antibacterial and osteoinductive capability of orthopedic materials via cation–π interaction mediated positive charge

Supplementary files

Article information

Article type
Communication
Submitted
20 Nov 2014
Accepted
10 Dec 2014
First published
10 Dec 2014

J. Mater. Chem. B, 2015,3, 733-737

Antibacterial and osteoinductive capability of orthopedic materials via cation–π interaction mediated positive charge

L. Shi, W. Zhang, K. Yang, H. Shi, D. Li, J. Liu, J. Ji and P. K. Chu, J. Mater. Chem. B, 2015, 3, 733 DOI: 10.1039/C4TB01924E

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