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Bismuth oxide aqueous colloidal nanoparticles inhibit Candida albicans growth and biofilm formation
Multiresistance among microorganisms to common antimicrobials has become one of the most significant concerns in modern medicine. Nanomaterials are a new alternative to successfully treat the multiresistant microorganisms. Nanostructured materials are used in many fields, including biological scienc...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639116/ https://www.ncbi.nlm.nih.gov/pubmed/23637533 http://dx.doi.org/10.2147/IJN.S38708 |
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author | Hernandez-Delgadillo, Rene Velasco-Arias, Donaji Martinez-Sanmiguel, Juan Jose Diaz, David Zumeta-Dube, Inti Arevalo-Niño, Katiushka Cabral-Romero, Claudio |
author_facet | Hernandez-Delgadillo, Rene Velasco-Arias, Donaji Martinez-Sanmiguel, Juan Jose Diaz, David Zumeta-Dube, Inti Arevalo-Niño, Katiushka Cabral-Romero, Claudio |
author_sort | Hernandez-Delgadillo, Rene |
collection | PubMed |
description | Multiresistance among microorganisms to common antimicrobials has become one of the most significant concerns in modern medicine. Nanomaterials are a new alternative to successfully treat the multiresistant microorganisms. Nanostructured materials are used in many fields, including biological sciences and medicine. Recently, it was demonstrated that the bactericidal activity of zero-valent bismuth colloidal nanoparticles inhibited the growth of Streptococcus mutans; however the antimycotic potential of bismuth nanostructured derivatives has not yet been studied. The main objective of this investigation was to analyze the fungicidal activity of bismuth oxide nanoparticles against Candida albicans, and their antibiofilm capabilities. Our results showed that aqueous colloidal bismuth oxide nanoparticles displayed antimicrobial activity against C. albicans growth (reducing colony size by 85%) and a complete inhibition of biofilm formation. These results are better than those obtained with chlorhexidine, nystatin, and terbinafine, the most effective oral antiseptic and commercial antifungal agents. In this work, we also compared the antimycotic activities of bulk bismuth oxide and bismuth nitrate, the precursor metallic salt. These results suggest that bismuth oxide colloidal nanoparticles could be a very interesting candidate as a fungicidal agent to be incorporated into an oral antiseptic. Additionally, we determined the minimum inhibitory concentration for the synthesized aqueous colloidal Bi(2)O(3) nanoparticles. |
format | Online Article Text |
id | pubmed-3639116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-36391162013-05-01 Bismuth oxide aqueous colloidal nanoparticles inhibit Candida albicans growth and biofilm formation Hernandez-Delgadillo, Rene Velasco-Arias, Donaji Martinez-Sanmiguel, Juan Jose Diaz, David Zumeta-Dube, Inti Arevalo-Niño, Katiushka Cabral-Romero, Claudio Int J Nanomedicine Original Research Multiresistance among microorganisms to common antimicrobials has become one of the most significant concerns in modern medicine. Nanomaterials are a new alternative to successfully treat the multiresistant microorganisms. Nanostructured materials are used in many fields, including biological sciences and medicine. Recently, it was demonstrated that the bactericidal activity of zero-valent bismuth colloidal nanoparticles inhibited the growth of Streptococcus mutans; however the antimycotic potential of bismuth nanostructured derivatives has not yet been studied. The main objective of this investigation was to analyze the fungicidal activity of bismuth oxide nanoparticles against Candida albicans, and their antibiofilm capabilities. Our results showed that aqueous colloidal bismuth oxide nanoparticles displayed antimicrobial activity against C. albicans growth (reducing colony size by 85%) and a complete inhibition of biofilm formation. These results are better than those obtained with chlorhexidine, nystatin, and terbinafine, the most effective oral antiseptic and commercial antifungal agents. In this work, we also compared the antimycotic activities of bulk bismuth oxide and bismuth nitrate, the precursor metallic salt. These results suggest that bismuth oxide colloidal nanoparticles could be a very interesting candidate as a fungicidal agent to be incorporated into an oral antiseptic. Additionally, we determined the minimum inhibitory concentration for the synthesized aqueous colloidal Bi(2)O(3) nanoparticles. Dove Medical Press 2013 2013-04-24 /pmc/articles/PMC3639116/ /pubmed/23637533 http://dx.doi.org/10.2147/IJN.S38708 Text en © 2013 Hernandez-Delgadillo et al, publisher and licensee Dove Medical Press Ltd This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited. |
spellingShingle | Original Research Hernandez-Delgadillo, Rene Velasco-Arias, Donaji Martinez-Sanmiguel, Juan Jose Diaz, David Zumeta-Dube, Inti Arevalo-Niño, Katiushka Cabral-Romero, Claudio Bismuth oxide aqueous colloidal nanoparticles inhibit Candida albicans growth and biofilm formation |
title | Bismuth oxide aqueous colloidal nanoparticles inhibit Candida albicans growth and biofilm formation |
title_full | Bismuth oxide aqueous colloidal nanoparticles inhibit Candida albicans growth and biofilm formation |
title_fullStr | Bismuth oxide aqueous colloidal nanoparticles inhibit Candida albicans growth and biofilm formation |
title_full_unstemmed | Bismuth oxide aqueous colloidal nanoparticles inhibit Candida albicans growth and biofilm formation |
title_short | Bismuth oxide aqueous colloidal nanoparticles inhibit Candida albicans growth and biofilm formation |
title_sort | bismuth oxide aqueous colloidal nanoparticles inhibit candida albicans growth and biofilm formation |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3639116/ https://www.ncbi.nlm.nih.gov/pubmed/23637533 http://dx.doi.org/10.2147/IJN.S38708 |
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