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Insights into the Antimicrobial Activity of Hydrated Cobaltmolybdate Doped with Copper

Molybdates are biocidal materials that can be useful in coating surfaces that are susceptible to contamination and the spread of microorganisms. The aim of this work was to investigate the effects of copper doping of hydrated cobalt molybdate, synthesized by the co-precipitation method, on its antib...

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Autores principales: Silva, Layane A. L., Silva, André A. L., Rios, Maria A. S., Brito, Manoel P., Araújo, Alyne R., Silva, Durcilene A., Peña-Garcia, Ramón R., Silva-Filho, Edson C., Magalhães, Janildo L., Matos, José M. E., Osajima, Josy A., Triboni, Eduardo R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7956662/
https://www.ncbi.nlm.nih.gov/pubmed/33652788
http://dx.doi.org/10.3390/molecules26051267
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author Silva, Layane A. L.
Silva, André A. L.
Rios, Maria A. S.
Brito, Manoel P.
Araújo, Alyne R.
Silva, Durcilene A.
Peña-Garcia, Ramón R.
Silva-Filho, Edson C.
Magalhães, Janildo L.
Matos, José M. E.
Osajima, Josy A.
Triboni, Eduardo R.
author_facet Silva, Layane A. L.
Silva, André A. L.
Rios, Maria A. S.
Brito, Manoel P.
Araújo, Alyne R.
Silva, Durcilene A.
Peña-Garcia, Ramón R.
Silva-Filho, Edson C.
Magalhães, Janildo L.
Matos, José M. E.
Osajima, Josy A.
Triboni, Eduardo R.
author_sort Silva, Layane A. L.
collection PubMed
description Molybdates are biocidal materials that can be useful in coating surfaces that are susceptible to contamination and the spread of microorganisms. The aim of this work was to investigate the effects of copper doping of hydrated cobalt molybdate, synthesized by the co-precipitation method, on its antibacterial activity and to elucidate the structural and morphological changes caused by the dopant in the material. The synthesized materials were characterized by PXRD, Fourier Transformed Infrared (FTIR), thermogravimetric analysis/differential scanning calorimetry (TG/DSC), and SEM-Energy Dispersive Spectroscopy (SEM-EDS). The antibacterial response of the materials was verified using the Minimum Inhibitory Concentration (MIC) employing the broth microdilution method. The size of the CoMoO(4)·1.03H(2)O microparticles gradually increased as the percentage of copper increased, decreasing the energy that is needed to promote the transition from the hydrated to the beta phase and changing the color of material. CoMoO(4)·1.03H(2)O obtained better bactericidal performance against the tested strains of Staphylococcus aureus (gram-positive) than Escherichia coli (gram-negative). However, an interesting point was that the use of copper as a doping agent for hydrated cobalt molybdate caused an increase of MIC value in the presence of E. coli and S. aureus strains. The study demonstrates the need for caution in the use of copper as a doping material in biocidal matrices, such as cobalt molybdate.
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spelling pubmed-79566622021-03-16 Insights into the Antimicrobial Activity of Hydrated Cobaltmolybdate Doped with Copper Silva, Layane A. L. Silva, André A. L. Rios, Maria A. S. Brito, Manoel P. Araújo, Alyne R. Silva, Durcilene A. Peña-Garcia, Ramón R. Silva-Filho, Edson C. Magalhães, Janildo L. Matos, José M. E. Osajima, Josy A. Triboni, Eduardo R. Molecules Article Molybdates are biocidal materials that can be useful in coating surfaces that are susceptible to contamination and the spread of microorganisms. The aim of this work was to investigate the effects of copper doping of hydrated cobalt molybdate, synthesized by the co-precipitation method, on its antibacterial activity and to elucidate the structural and morphological changes caused by the dopant in the material. The synthesized materials were characterized by PXRD, Fourier Transformed Infrared (FTIR), thermogravimetric analysis/differential scanning calorimetry (TG/DSC), and SEM-Energy Dispersive Spectroscopy (SEM-EDS). The antibacterial response of the materials was verified using the Minimum Inhibitory Concentration (MIC) employing the broth microdilution method. The size of the CoMoO(4)·1.03H(2)O microparticles gradually increased as the percentage of copper increased, decreasing the energy that is needed to promote the transition from the hydrated to the beta phase and changing the color of material. CoMoO(4)·1.03H(2)O obtained better bactericidal performance against the tested strains of Staphylococcus aureus (gram-positive) than Escherichia coli (gram-negative). However, an interesting point was that the use of copper as a doping agent for hydrated cobalt molybdate caused an increase of MIC value in the presence of E. coli and S. aureus strains. The study demonstrates the need for caution in the use of copper as a doping material in biocidal matrices, such as cobalt molybdate. MDPI 2021-02-26 /pmc/articles/PMC7956662/ /pubmed/33652788 http://dx.doi.org/10.3390/molecules26051267 Text en © 2021 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 Article
Silva, Layane A. L.
Silva, André A. L.
Rios, Maria A. S.
Brito, Manoel P.
Araújo, Alyne R.
Silva, Durcilene A.
Peña-Garcia, Ramón R.
Silva-Filho, Edson C.
Magalhães, Janildo L.
Matos, José M. E.
Osajima, Josy A.
Triboni, Eduardo R.
Insights into the Antimicrobial Activity of Hydrated Cobaltmolybdate Doped with Copper
title Insights into the Antimicrobial Activity of Hydrated Cobaltmolybdate Doped with Copper
title_full Insights into the Antimicrobial Activity of Hydrated Cobaltmolybdate Doped with Copper
title_fullStr Insights into the Antimicrobial Activity of Hydrated Cobaltmolybdate Doped with Copper
title_full_unstemmed Insights into the Antimicrobial Activity of Hydrated Cobaltmolybdate Doped with Copper
title_short Insights into the Antimicrobial Activity of Hydrated Cobaltmolybdate Doped with Copper
title_sort insights into the antimicrobial activity of hydrated cobaltmolybdate doped with copper
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7956662/
https://www.ncbi.nlm.nih.gov/pubmed/33652788
http://dx.doi.org/10.3390/molecules26051267
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