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In Vitro Antimicrobial Activity of the Decontaminant HybenX(®) Compared to Chlorhexidine and Sodium Hypochlorite against Common Bacterial and Yeast Pathogens

The recent increase in infections mediated by drug-resistant bacterial and fungal pathogens underlines the urgent need for novel antimicrobial compounds. In this study, the antimicrobial activity (inhibitory and cidal) of HybenX(®), a novel dessicating agent, in comparison with commonly used sodium...

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Autores principales: Antonelli, Alberto, Giovannini, Luca, Baccani, Ilaria, Giuliani, Valentina, Pace, Riccardo, Rossolini, Gian Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963449/
https://www.ncbi.nlm.nih.gov/pubmed/31627304
http://dx.doi.org/10.3390/antibiotics8040188
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author Antonelli, Alberto
Giovannini, Luca
Baccani, Ilaria
Giuliani, Valentina
Pace, Riccardo
Rossolini, Gian Maria
author_facet Antonelli, Alberto
Giovannini, Luca
Baccani, Ilaria
Giuliani, Valentina
Pace, Riccardo
Rossolini, Gian Maria
author_sort Antonelli, Alberto
collection PubMed
description The recent increase in infections mediated by drug-resistant bacterial and fungal pathogens underlines the urgent need for novel antimicrobial compounds. In this study, the antimicrobial activity (inhibitory and cidal) of HybenX(®), a novel dessicating agent, in comparison with commonly used sodium hypochlorite and chlorhexidine, against a collection of bacterial and yeast strains representative of the most common human pathogenic species was evaluated. The minimal inhibitory, bactericidal, and fungicidal concentrations (MIC, MBC, and MFC, respectively) of the three different antimicrobial agents were evaluated by broth microdilution assays, followed by subculturing of suitable dilutions. HybenX(®) was active against 26 reference strains representative of staphylococci, enterococci, Enterobacterales, Gram-negative nonfermenters, and yeasts, although at higher concentrations than sodium hypochlorite and chlorhexidine. HybenX(®) MICs were 0.39% for bacteria (with MBCs ranging between 0.39% and 0.78%), and 0.1–0.78% for yeasts (with MFCs ranging between 0.78% and 1.6%). HybenX(®) exhibited potent inhibitory and cidal activity at low concentrations against several bacterial and yeast pathogens. These findings suggest that HybenX(®) could be of interest for the treatment of parodontal and endodontic infections and also for bacterial and fungal infections of other mucous membranes and skin as an alternative to sodium hypochlorite and chlorhexidine.
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spelling pubmed-69634492020-01-30 In Vitro Antimicrobial Activity of the Decontaminant HybenX(®) Compared to Chlorhexidine and Sodium Hypochlorite against Common Bacterial and Yeast Pathogens Antonelli, Alberto Giovannini, Luca Baccani, Ilaria Giuliani, Valentina Pace, Riccardo Rossolini, Gian Maria Antibiotics (Basel) Brief Report The recent increase in infections mediated by drug-resistant bacterial and fungal pathogens underlines the urgent need for novel antimicrobial compounds. In this study, the antimicrobial activity (inhibitory and cidal) of HybenX(®), a novel dessicating agent, in comparison with commonly used sodium hypochlorite and chlorhexidine, against a collection of bacterial and yeast strains representative of the most common human pathogenic species was evaluated. The minimal inhibitory, bactericidal, and fungicidal concentrations (MIC, MBC, and MFC, respectively) of the three different antimicrobial agents were evaluated by broth microdilution assays, followed by subculturing of suitable dilutions. HybenX(®) was active against 26 reference strains representative of staphylococci, enterococci, Enterobacterales, Gram-negative nonfermenters, and yeasts, although at higher concentrations than sodium hypochlorite and chlorhexidine. HybenX(®) MICs were 0.39% for bacteria (with MBCs ranging between 0.39% and 0.78%), and 0.1–0.78% for yeasts (with MFCs ranging between 0.78% and 1.6%). HybenX(®) exhibited potent inhibitory and cidal activity at low concentrations against several bacterial and yeast pathogens. These findings suggest that HybenX(®) could be of interest for the treatment of parodontal and endodontic infections and also for bacterial and fungal infections of other mucous membranes and skin as an alternative to sodium hypochlorite and chlorhexidine. MDPI 2019-10-17 /pmc/articles/PMC6963449/ /pubmed/31627304 http://dx.doi.org/10.3390/antibiotics8040188 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Brief Report
Antonelli, Alberto
Giovannini, Luca
Baccani, Ilaria
Giuliani, Valentina
Pace, Riccardo
Rossolini, Gian Maria
In Vitro Antimicrobial Activity of the Decontaminant HybenX(®) Compared to Chlorhexidine and Sodium Hypochlorite against Common Bacterial and Yeast Pathogens
title In Vitro Antimicrobial Activity of the Decontaminant HybenX(®) Compared to Chlorhexidine and Sodium Hypochlorite against Common Bacterial and Yeast Pathogens
title_full In Vitro Antimicrobial Activity of the Decontaminant HybenX(®) Compared to Chlorhexidine and Sodium Hypochlorite against Common Bacterial and Yeast Pathogens
title_fullStr In Vitro Antimicrobial Activity of the Decontaminant HybenX(®) Compared to Chlorhexidine and Sodium Hypochlorite against Common Bacterial and Yeast Pathogens
title_full_unstemmed In Vitro Antimicrobial Activity of the Decontaminant HybenX(®) Compared to Chlorhexidine and Sodium Hypochlorite against Common Bacterial and Yeast Pathogens
title_short In Vitro Antimicrobial Activity of the Decontaminant HybenX(®) Compared to Chlorhexidine and Sodium Hypochlorite against Common Bacterial and Yeast Pathogens
title_sort in vitro antimicrobial activity of the decontaminant hybenx(®) compared to chlorhexidine and sodium hypochlorite against common bacterial and yeast pathogens
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6963449/
https://www.ncbi.nlm.nih.gov/pubmed/31627304
http://dx.doi.org/10.3390/antibiotics8040188
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