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Cu-Doped Hollow Bioactive Glass Nanoparticles for Bone Infection Treatment
In search of new approaches to treat bone infection and prevent drug resistance development, a nanosystem based on hollow bioactive glass nanoparticles (HBGN) of composition 79.5SiO(2)-(18-x)CaO-2.5P(2)O(5)-xCuO (x = 0, 2.5 or 5 mol-% CuO) was developed. The objective of the study was to evaluate th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9027665/ https://www.ncbi.nlm.nih.gov/pubmed/35456679 http://dx.doi.org/10.3390/pharmaceutics14040845 |
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author | Jiménez-Holguín, Javier Sánchez-Salcedo, Sandra Cicuéndez, Mónica Vallet-Regí, María Salinas, Antonio J. |
author_facet | Jiménez-Holguín, Javier Sánchez-Salcedo, Sandra Cicuéndez, Mónica Vallet-Regí, María Salinas, Antonio J. |
author_sort | Jiménez-Holguín, Javier |
collection | PubMed |
description | In search of new approaches to treat bone infection and prevent drug resistance development, a nanosystem based on hollow bioactive glass nanoparticles (HBGN) of composition 79.5SiO(2)-(18-x)CaO-2.5P(2)O(5)-xCuO (x = 0, 2.5 or 5 mol-% CuO) was developed. The objective of the study was to evaluate the capacity of the HBGN to be used as a nanocarrier of the broad-spectrum antibiotic danofloxacin and source of bactericidal Cu(2+) ions. Core-shell nanoparticles with specific surface areas close to 800 m(2)/g and pore volumes around 1 cm(3)/g were obtained by using hexadecyltrimethylammonium bromide (CTAB) and poly(styrene)-block-poly(acrylic acid) (PS-b-PAA) as structure-directing agents. Flow cytometry studies showed the cytocompatibility of the nanoparticles in MC3T3-E1 pre-osteoblastic cell cultures. Ion release studies confirmed the release of non-cytotoxic concentrations of Cu(2+) ions within the therapeutic range. Moreover, it was shown that the inclusion of copper in the system resulted in a more gradual release of danofloxacin that was extended over one week. The bactericidal activity of the nanosystem was evaluated with E. coli and S. aureus strains. Nanoparticles with copper were not able to reduce bacterial viability by themselves and Cu-free HBGN failed to reduce bacterial growth, despite releasing higher antibiotic concentrations. However, HBGN enriched with copper and danofloxacin drastically reduced bacterial growth in sessile, planktonic and biofilm states, which was attributed to a synergistic effect between the action of Cu(2+) ions and danofloxacin. Therefore, the nanosystem here investigated is a promising candidate as an alternative for the local treatment of bone infections. |
format | Online Article Text |
id | pubmed-9027665 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90276652022-04-23 Cu-Doped Hollow Bioactive Glass Nanoparticles for Bone Infection Treatment Jiménez-Holguín, Javier Sánchez-Salcedo, Sandra Cicuéndez, Mónica Vallet-Regí, María Salinas, Antonio J. Pharmaceutics Article In search of new approaches to treat bone infection and prevent drug resistance development, a nanosystem based on hollow bioactive glass nanoparticles (HBGN) of composition 79.5SiO(2)-(18-x)CaO-2.5P(2)O(5)-xCuO (x = 0, 2.5 or 5 mol-% CuO) was developed. The objective of the study was to evaluate the capacity of the HBGN to be used as a nanocarrier of the broad-spectrum antibiotic danofloxacin and source of bactericidal Cu(2+) ions. Core-shell nanoparticles with specific surface areas close to 800 m(2)/g and pore volumes around 1 cm(3)/g were obtained by using hexadecyltrimethylammonium bromide (CTAB) and poly(styrene)-block-poly(acrylic acid) (PS-b-PAA) as structure-directing agents. Flow cytometry studies showed the cytocompatibility of the nanoparticles in MC3T3-E1 pre-osteoblastic cell cultures. Ion release studies confirmed the release of non-cytotoxic concentrations of Cu(2+) ions within the therapeutic range. Moreover, it was shown that the inclusion of copper in the system resulted in a more gradual release of danofloxacin that was extended over one week. The bactericidal activity of the nanosystem was evaluated with E. coli and S. aureus strains. Nanoparticles with copper were not able to reduce bacterial viability by themselves and Cu-free HBGN failed to reduce bacterial growth, despite releasing higher antibiotic concentrations. However, HBGN enriched with copper and danofloxacin drastically reduced bacterial growth in sessile, planktonic and biofilm states, which was attributed to a synergistic effect between the action of Cu(2+) ions and danofloxacin. Therefore, the nanosystem here investigated is a promising candidate as an alternative for the local treatment of bone infections. MDPI 2022-04-12 /pmc/articles/PMC9027665/ /pubmed/35456679 http://dx.doi.org/10.3390/pharmaceutics14040845 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Jiménez-Holguín, Javier Sánchez-Salcedo, Sandra Cicuéndez, Mónica Vallet-Regí, María Salinas, Antonio J. Cu-Doped Hollow Bioactive Glass Nanoparticles for Bone Infection Treatment |
title | Cu-Doped Hollow Bioactive Glass Nanoparticles for Bone Infection Treatment |
title_full | Cu-Doped Hollow Bioactive Glass Nanoparticles for Bone Infection Treatment |
title_fullStr | Cu-Doped Hollow Bioactive Glass Nanoparticles for Bone Infection Treatment |
title_full_unstemmed | Cu-Doped Hollow Bioactive Glass Nanoparticles for Bone Infection Treatment |
title_short | Cu-Doped Hollow Bioactive Glass Nanoparticles for Bone Infection Treatment |
title_sort | cu-doped hollow bioactive glass nanoparticles for bone infection treatment |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9027665/ https://www.ncbi.nlm.nih.gov/pubmed/35456679 http://dx.doi.org/10.3390/pharmaceutics14040845 |
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