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Incorporation of Chloramphenicol Loaded Hydroxyapatite Nanoparticles into Polylactide
Chloramphenicol (CAM) has been encapsulated into hydroxyapatite nanoparticles displaying different morphologies and crystallinities. The process was based on typical precipitation of solutions containing phosphate and calcium ions and the addition of CAM once the hydroxyapatite nuclei were formed. T...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6834152/ https://www.ncbi.nlm.nih.gov/pubmed/31614695 http://dx.doi.org/10.3390/ijms20205056 |
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author | Rivas, Manuel Pelechà, Marc Franco, Lourdes Turon, Pau Alemán, Carlos del Valle, Luis J. Puiggalí, Jordi |
author_facet | Rivas, Manuel Pelechà, Marc Franco, Lourdes Turon, Pau Alemán, Carlos del Valle, Luis J. Puiggalí, Jordi |
author_sort | Rivas, Manuel |
collection | PubMed |
description | Chloramphenicol (CAM) has been encapsulated into hydroxyapatite nanoparticles displaying different morphologies and crystallinities. The process was based on typical precipitation of solutions containing phosphate and calcium ions and the addition of CAM once the hydroxyapatite nuclei were formed. This procedure favored a disposition of the drug into the bulk parts of the nanoparticles and led to a fast release in aqueous media. Clear antibacterial activity was derived, being slightly higher for the amorphous samples due to their higher encapsulation efficiency. Polylactide (PLA) microfibers incorporating CAM encapsulated in hydroxyapatite nanoparticles were prepared by the electrospinning technique and under optimized conditions. Drug release experiments demonstrated that only a small percentage of the loaded CAM could be delivered to an aqueous PBS medium. This amount was enough to render an immediate bacteriostatic effect without causing a cytotoxic effect on osteoblast-like, fibroblasts, and epithelial cells. Therefore, the prepared scaffolds were able to retain CAM-loaded nanoparticles, being a reservoir that should allow a prolonged release depending on the polymer degradation rate. The studied system may have promising applications for the treatment of cancer since CAM has been proposed as a new antitumor drug. |
format | Online Article Text |
id | pubmed-6834152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68341522019-11-25 Incorporation of Chloramphenicol Loaded Hydroxyapatite Nanoparticles into Polylactide Rivas, Manuel Pelechà, Marc Franco, Lourdes Turon, Pau Alemán, Carlos del Valle, Luis J. Puiggalí, Jordi Int J Mol Sci Article Chloramphenicol (CAM) has been encapsulated into hydroxyapatite nanoparticles displaying different morphologies and crystallinities. The process was based on typical precipitation of solutions containing phosphate and calcium ions and the addition of CAM once the hydroxyapatite nuclei were formed. This procedure favored a disposition of the drug into the bulk parts of the nanoparticles and led to a fast release in aqueous media. Clear antibacterial activity was derived, being slightly higher for the amorphous samples due to their higher encapsulation efficiency. Polylactide (PLA) microfibers incorporating CAM encapsulated in hydroxyapatite nanoparticles were prepared by the electrospinning technique and under optimized conditions. Drug release experiments demonstrated that only a small percentage of the loaded CAM could be delivered to an aqueous PBS medium. This amount was enough to render an immediate bacteriostatic effect without causing a cytotoxic effect on osteoblast-like, fibroblasts, and epithelial cells. Therefore, the prepared scaffolds were able to retain CAM-loaded nanoparticles, being a reservoir that should allow a prolonged release depending on the polymer degradation rate. The studied system may have promising applications for the treatment of cancer since CAM has been proposed as a new antitumor drug. MDPI 2019-10-11 /pmc/articles/PMC6834152/ /pubmed/31614695 http://dx.doi.org/10.3390/ijms20205056 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 | Article Rivas, Manuel Pelechà, Marc Franco, Lourdes Turon, Pau Alemán, Carlos del Valle, Luis J. Puiggalí, Jordi Incorporation of Chloramphenicol Loaded Hydroxyapatite Nanoparticles into Polylactide |
title | Incorporation of Chloramphenicol Loaded Hydroxyapatite Nanoparticles into Polylactide |
title_full | Incorporation of Chloramphenicol Loaded Hydroxyapatite Nanoparticles into Polylactide |
title_fullStr | Incorporation of Chloramphenicol Loaded Hydroxyapatite Nanoparticles into Polylactide |
title_full_unstemmed | Incorporation of Chloramphenicol Loaded Hydroxyapatite Nanoparticles into Polylactide |
title_short | Incorporation of Chloramphenicol Loaded Hydroxyapatite Nanoparticles into Polylactide |
title_sort | incorporation of chloramphenicol loaded hydroxyapatite nanoparticles into polylactide |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6834152/ https://www.ncbi.nlm.nih.gov/pubmed/31614695 http://dx.doi.org/10.3390/ijms20205056 |
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