A Chlorhexidine-releasing Epoxy-based Coating On Tytanium Implants Prevents Staphylococcus Aureus Experimental Biomaterial-associated Infection

M. Riool, A. J. Dirks, V. Jaspers, L. de Boer, T. J. A. Loontjens, C. M. van der Loos, S. Florquin, I. Apachitei, L. N. D. Rijk, H. A. Keul, S. A. J. Zaat*

*Bijbehorende auteur voor dit werk

OnderzoeksoutputAcademicpeer review

26 Citaten (Scopus)
94 Downloads (Pure)

Samenvatting

Prevention of biomaterial-associated infections (BAI) remains a challenging problem, in particular due to the increased risk of resistance development with the current antibiotic-based strategies. Metallic orthopaedic devices, such as non-cemented implants, are often inserted under high mechanical stress. These non-cemented implants cannot be protected by e.g. antibiotic-releasing bone cement or other antimicrobial approaches, such as the use of bioactive glass. Therefore, in order to avoid abrasion during implantation procedures, we developed an antimicrobial coating with great mechanical stability for orthopaedic implants, to prevent Staphylococcus aureus BAI. We incorporated 5 and 10 wt % chlorhexidine in a novel mechanically stable epoxy-based coating, designated CHX5 and CHX10, respectively. The coatings displayed potent bactericidal activity in vitro against S. aureus, with over 80 % of the release (19 mu g/cm(2) for CHX5 and 41 mu g/cm(2) for CHX10) occurring within the first 24 h. In mice, the CHX10 coating significantly reduced the number of CFU (colony forming units), both on the implants and in the peri-implant tissues, 1 d after S. aureus challenge. The CHX10-coated implants were well-tolerated by the animals, with no signs of toxicity observed by histological analysis. Moreover, the coating significantly reduced the frequency of culture-positive tissues 1 d, and of culture-positive implants 1 and 4 d after challenge. In summary, the chlorhexidine-releasing mechanically stable epoxy-based CHX10 coating prevented implant colonisation and S. aureus BAI in mice and has good prospects for clinical development.

Originele taal-2English
Pagina's (van-tot)143-157
Aantal pagina's15
TijdschriftEuropean cells & materials
Volume33
DOI's
StatusPublished - 2017

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