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Antibacterial Activities of Azole Complexes Combined with Silver Nanoparticles
Growing antimicrobial resistance is considered a potential threat for human health security by health organizations, such as the WHO, CDC and FDA, pointing to MRSA as an example. New antibacterial drugs and complex derivatives are needed to combat the development of bacterial resistance. Six new cop...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017516/ https://www.ncbi.nlm.nih.gov/pubmed/29419803 http://dx.doi.org/10.3390/molecules23020361 |
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author | Bello-Vieda, Nestor J. Pastrana, Homero F. Garavito, Manuel F. Ávila, Alba G. Celis, Adriana M. Muñoz-Castro, Alvaro Restrepo, Silvia Hurtado, John J. |
author_facet | Bello-Vieda, Nestor J. Pastrana, Homero F. Garavito, Manuel F. Ávila, Alba G. Celis, Adriana M. Muñoz-Castro, Alvaro Restrepo, Silvia Hurtado, John J. |
author_sort | Bello-Vieda, Nestor J. |
collection | PubMed |
description | Growing antimicrobial resistance is considered a potential threat for human health security by health organizations, such as the WHO, CDC and FDA, pointing to MRSA as an example. New antibacterial drugs and complex derivatives are needed to combat the development of bacterial resistance. Six new copper and cobalt complexes of azole derivatives were synthesized and isolated as air-stable solids and characterized by melting point analyses, elemental analyses, thermogravimetric analyses (TGA), and infrared and ultraviolet/visible spectroscopy. The analyses and spectral data showed that the complexes had 1:1 (M:L) stoichiometries and tetrahedral geometries, the latter being supported by DFT calculations. The antibacterial activities of the metal complexes by themselves and combined with silver nanoparticles (AgNPs; 2 μg mL(−1)) were assessed in vitro by broth microdilution assays against eight bacterial strains of clinical relevance. The results showed that the complexes alone exhibited moderate antibacterial activities. However, when the metal complexes were combined with AgNPs, their antibacterial activities increased (up to 10-fold in the case of complex 5), while human cell viabilities were maintained. The minimum inhibitory concentration (MIC(50)) values were in the range of 25–500 μg mL(−1). This study thus presents novel approaches for the design of materials for fighting bacterial resistance. The use of azole complexes combined with AgNPs provides a new alternative against bacterial infections, especially when current treatments are associated with the rapid development of antibiotic resistance. |
format | Online Article Text |
id | pubmed-6017516 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60175162018-11-13 Antibacterial Activities of Azole Complexes Combined with Silver Nanoparticles Bello-Vieda, Nestor J. Pastrana, Homero F. Garavito, Manuel F. Ávila, Alba G. Celis, Adriana M. Muñoz-Castro, Alvaro Restrepo, Silvia Hurtado, John J. Molecules Article Growing antimicrobial resistance is considered a potential threat for human health security by health organizations, such as the WHO, CDC and FDA, pointing to MRSA as an example. New antibacterial drugs and complex derivatives are needed to combat the development of bacterial resistance. Six new copper and cobalt complexes of azole derivatives were synthesized and isolated as air-stable solids and characterized by melting point analyses, elemental analyses, thermogravimetric analyses (TGA), and infrared and ultraviolet/visible spectroscopy. The analyses and spectral data showed that the complexes had 1:1 (M:L) stoichiometries and tetrahedral geometries, the latter being supported by DFT calculations. The antibacterial activities of the metal complexes by themselves and combined with silver nanoparticles (AgNPs; 2 μg mL(−1)) were assessed in vitro by broth microdilution assays against eight bacterial strains of clinical relevance. The results showed that the complexes alone exhibited moderate antibacterial activities. However, when the metal complexes were combined with AgNPs, their antibacterial activities increased (up to 10-fold in the case of complex 5), while human cell viabilities were maintained. The minimum inhibitory concentration (MIC(50)) values were in the range of 25–500 μg mL(−1). This study thus presents novel approaches for the design of materials for fighting bacterial resistance. The use of azole complexes combined with AgNPs provides a new alternative against bacterial infections, especially when current treatments are associated with the rapid development of antibiotic resistance. MDPI 2018-02-08 /pmc/articles/PMC6017516/ /pubmed/29419803 http://dx.doi.org/10.3390/molecules23020361 Text en © 2018 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 Bello-Vieda, Nestor J. Pastrana, Homero F. Garavito, Manuel F. Ávila, Alba G. Celis, Adriana M. Muñoz-Castro, Alvaro Restrepo, Silvia Hurtado, John J. Antibacterial Activities of Azole Complexes Combined with Silver Nanoparticles |
title | Antibacterial Activities of Azole Complexes Combined with Silver Nanoparticles |
title_full | Antibacterial Activities of Azole Complexes Combined with Silver Nanoparticles |
title_fullStr | Antibacterial Activities of Azole Complexes Combined with Silver Nanoparticles |
title_full_unstemmed | Antibacterial Activities of Azole Complexes Combined with Silver Nanoparticles |
title_short | Antibacterial Activities of Azole Complexes Combined with Silver Nanoparticles |
title_sort | antibacterial activities of azole complexes combined with silver nanoparticles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017516/ https://www.ncbi.nlm.nih.gov/pubmed/29419803 http://dx.doi.org/10.3390/molecules23020361 |
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