effective and biocompatible antibiofilm coating for central venous catheter

The aim of this study was to investigate the in vitro and in vivo efficacy and the tissue reaction of an antibiofilm coating composed of xylitol, triclosan, and polyhexamethylene biguanide. The antimicrobial activity was analyzed by a turbidimetric method. Scanning electron microscopy was used to ev...

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Published inCanadian journal of microbiology Vol. 61; no. 5; pp. 357 - 365
Main Authors Silva Paes Leme, Annelisa Farah, Ferreira, Aline Siqueira, Alves, Fernanda Aparecida Oliveira, de Azevedo, Bruna Martinho, de Bretas, Liza Porcaro, Farias, Rogerio Estevam, Oliveira, Murilo Gomes, Raposo, Nádia Rezende Barbosa
Format Journal Article
LanguageEnglish
Published Canada NRC Research Press 01.05.2015
Canadian Science Publishing NRC Research Press
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Summary:The aim of this study was to investigate the in vitro and in vivo efficacy and the tissue reaction of an antibiofilm coating composed of xylitol, triclosan, and polyhexamethylene biguanide. The antimicrobial activity was analyzed by a turbidimetric method. Scanning electron microscopy was used to evaluate the antiadherent property of central venous catheter (CVC) fragments impregnated with an antibiofilm coating (I-CVC) in comparison with noncoated CVC (NC-CVC) fragments. Two in vivo assays using subcutaneous implantation of NC-CVC and I-CVC fragments in the dorsal area of rats were performed. The first assay comprised hematological and microbiological analysis. The second assay evaluated tissue response by examining the inflammatory reactions after 7 and 21 days. The formulation displayed antimicrobial activity against all tested strains. A biofilm disaggregation with significant reduction of microorganism’s adherence in I-CVC fragments was observed. In vivo antiadherence results demonstrated a reduction of early biofilm formation of Staphylococcus aureus ATCC 25923, mainly in an external surface of the I-CVC, in comparison with the NC-CVC. All animals displayed negative hemoculture. No significant tissue reaction was observed, indicating that the antibiofilm formulation could be considered biocompatible. The use of I-CVC could decrease the probability of development of localized or systemic infections.
Bibliography:http://dx.doi.org/10.1139/cjm-2014-0783
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ISSN:1480-3275
0008-4166
1480-3275
DOI:10.1139/cjm-2014-0783