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Nanostructured ZnO as Multifunctional Carrier for a Green Antibacterial Drug Delivery System—A Feasibility Study
The physico–chemical and biological properties of nanostructured ZnO are combined with the non-toxic and eco-friendly features of the scCO(2)-mediated drug loading technique to develop a multifunctional antimicrobial drug delivery system for potential applications in wound healing. Two nanostructure...
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/PMC6473990/ https://www.ncbi.nlm.nih.gov/pubmed/30862002 http://dx.doi.org/10.3390/nano9030407 |
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author | Leone, Federica Cataldo, Roberta Mohamed, Sara S. Y. Manna, Luigi Banchero, Mauro Ronchetti, Silvia Mandras, Narcisa Tullio, Vivian Cavalli, Roberta Onida, Barbara |
author_facet | Leone, Federica Cataldo, Roberta Mohamed, Sara S. Y. Manna, Luigi Banchero, Mauro Ronchetti, Silvia Mandras, Narcisa Tullio, Vivian Cavalli, Roberta Onida, Barbara |
author_sort | Leone, Federica |
collection | PubMed |
description | The physico–chemical and biological properties of nanostructured ZnO are combined with the non-toxic and eco-friendly features of the scCO(2)-mediated drug loading technique to develop a multifunctional antimicrobial drug delivery system for potential applications in wound healing. Two nanostructured ZnO (NsZnO) with different morphologies were prepared through wet organic-solvent-free processes and characterized by means of powder X-ray diffraction, field emission scanning electron microscopy (FESEM), and nitrogen adsorption analysis. The antimicrobial activity of the two samples against different microbial strains was investigated together with the in vitro Zn(2+) release. The results indicated that the two ZnO nanostructures exhibited the following activity: S. aureus > C. albicans > K. pneumoniae. A correlation between the antimicrobial activity, the physico–chemical properties (specific surface area and crystal size) and the Zn(2+) ion release was found. Ibuprofen was, for the first time, loaded on the NsZnO carriers with a supercritical CO(2)-mediated drug impregnation process and in vitro dissolution studies of the loaded drug were performed. A successful loading up to 14% w/w of ibuprofen in its amorphous form was obtained. A preliminary drug release test showed that up to 68% of the loaded ibuprofen could be delivered to a biological medium, confirming the feasibility of using NsZnO as a multifunctional antimicrobial drug carrier. |
format | Online Article Text |
id | pubmed-6473990 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64739902019-05-03 Nanostructured ZnO as Multifunctional Carrier for a Green Antibacterial Drug Delivery System—A Feasibility Study Leone, Federica Cataldo, Roberta Mohamed, Sara S. Y. Manna, Luigi Banchero, Mauro Ronchetti, Silvia Mandras, Narcisa Tullio, Vivian Cavalli, Roberta Onida, Barbara Nanomaterials (Basel) Article The physico–chemical and biological properties of nanostructured ZnO are combined with the non-toxic and eco-friendly features of the scCO(2)-mediated drug loading technique to develop a multifunctional antimicrobial drug delivery system for potential applications in wound healing. Two nanostructured ZnO (NsZnO) with different morphologies were prepared through wet organic-solvent-free processes and characterized by means of powder X-ray diffraction, field emission scanning electron microscopy (FESEM), and nitrogen adsorption analysis. The antimicrobial activity of the two samples against different microbial strains was investigated together with the in vitro Zn(2+) release. The results indicated that the two ZnO nanostructures exhibited the following activity: S. aureus > C. albicans > K. pneumoniae. A correlation between the antimicrobial activity, the physico–chemical properties (specific surface area and crystal size) and the Zn(2+) ion release was found. Ibuprofen was, for the first time, loaded on the NsZnO carriers with a supercritical CO(2)-mediated drug impregnation process and in vitro dissolution studies of the loaded drug were performed. A successful loading up to 14% w/w of ibuprofen in its amorphous form was obtained. A preliminary drug release test showed that up to 68% of the loaded ibuprofen could be delivered to a biological medium, confirming the feasibility of using NsZnO as a multifunctional antimicrobial drug carrier. MDPI 2019-03-11 /pmc/articles/PMC6473990/ /pubmed/30862002 http://dx.doi.org/10.3390/nano9030407 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 Leone, Federica Cataldo, Roberta Mohamed, Sara S. Y. Manna, Luigi Banchero, Mauro Ronchetti, Silvia Mandras, Narcisa Tullio, Vivian Cavalli, Roberta Onida, Barbara Nanostructured ZnO as Multifunctional Carrier for a Green Antibacterial Drug Delivery System—A Feasibility Study |
title | Nanostructured ZnO as Multifunctional Carrier for a Green Antibacterial Drug Delivery System—A Feasibility Study |
title_full | Nanostructured ZnO as Multifunctional Carrier for a Green Antibacterial Drug Delivery System—A Feasibility Study |
title_fullStr | Nanostructured ZnO as Multifunctional Carrier for a Green Antibacterial Drug Delivery System—A Feasibility Study |
title_full_unstemmed | Nanostructured ZnO as Multifunctional Carrier for a Green Antibacterial Drug Delivery System—A Feasibility Study |
title_short | Nanostructured ZnO as Multifunctional Carrier for a Green Antibacterial Drug Delivery System—A Feasibility Study |
title_sort | nanostructured zno as multifunctional carrier for a green antibacterial drug delivery system—a feasibility study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6473990/ https://www.ncbi.nlm.nih.gov/pubmed/30862002 http://dx.doi.org/10.3390/nano9030407 |
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