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A novel synthetic approach of cerium oxide nanoparticles with improved biomedical activity
Cerium oxide nanoparticles (CNPs) are novel synthetic antioxidant agents proposed for treating oxidative stress-related diseases. The synthesis of high-quality CNPs for biomedical applications remains a challenging task. A major concern for a safe use of CNPs as pharmacological agents is their tende...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498533/ https://www.ncbi.nlm.nih.gov/pubmed/28680107 http://dx.doi.org/10.1038/s41598-017-04098-6 |
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author | Caputo, Fanny Mameli, Marta Sienkiewicz, Andrzej Licoccia, Silvia Stellacci, Francesco Ghibelli, Lina Traversa, Enrico |
author_facet | Caputo, Fanny Mameli, Marta Sienkiewicz, Andrzej Licoccia, Silvia Stellacci, Francesco Ghibelli, Lina Traversa, Enrico |
author_sort | Caputo, Fanny |
collection | PubMed |
description | Cerium oxide nanoparticles (CNPs) are novel synthetic antioxidant agents proposed for treating oxidative stress-related diseases. The synthesis of high-quality CNPs for biomedical applications remains a challenging task. A major concern for a safe use of CNPs as pharmacological agents is their tendency to agglomerate. Herein we present a simple direct precipitation approach, exploiting ethylene glycol as synthesis co-factor, to synthesize at room temperature nanocrystalline sub-10 nm CNPs, followed by a surface silanization approach to improve nanoparticle dispersibility in biological fluids. CNPs were characterized using transmission electron microscopy (TEM) observations, X-ray diffraction (XRD) analysis, thermogravimetric analysis (TGA), Fourier-transform infrared (FT-IR) spectroscopy, proton nuclear magnetic resonance ((1)H-NMR) spectroscopy, dynamic light scattering (DLS) and zeta potential measurements. CNP redox activity was studied in abiotic systems using electron spin resonance (ESR) measurements, and in vitro on human cell models. In-situ silanization improved CNP colloidal stability, in comparison with non-functionalized particles, and allowed at the same time improving their original biological activity, yielding thus functionalized CNPs suitable for biomedical applications. |
format | Online Article Text |
id | pubmed-5498533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54985332017-07-10 A novel synthetic approach of cerium oxide nanoparticles with improved biomedical activity Caputo, Fanny Mameli, Marta Sienkiewicz, Andrzej Licoccia, Silvia Stellacci, Francesco Ghibelli, Lina Traversa, Enrico Sci Rep Article Cerium oxide nanoparticles (CNPs) are novel synthetic antioxidant agents proposed for treating oxidative stress-related diseases. The synthesis of high-quality CNPs for biomedical applications remains a challenging task. A major concern for a safe use of CNPs as pharmacological agents is their tendency to agglomerate. Herein we present a simple direct precipitation approach, exploiting ethylene glycol as synthesis co-factor, to synthesize at room temperature nanocrystalline sub-10 nm CNPs, followed by a surface silanization approach to improve nanoparticle dispersibility in biological fluids. CNPs were characterized using transmission electron microscopy (TEM) observations, X-ray diffraction (XRD) analysis, thermogravimetric analysis (TGA), Fourier-transform infrared (FT-IR) spectroscopy, proton nuclear magnetic resonance ((1)H-NMR) spectroscopy, dynamic light scattering (DLS) and zeta potential measurements. CNP redox activity was studied in abiotic systems using electron spin resonance (ESR) measurements, and in vitro on human cell models. In-situ silanization improved CNP colloidal stability, in comparison with non-functionalized particles, and allowed at the same time improving their original biological activity, yielding thus functionalized CNPs suitable for biomedical applications. Nature Publishing Group UK 2017-07-05 /pmc/articles/PMC5498533/ /pubmed/28680107 http://dx.doi.org/10.1038/s41598-017-04098-6 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Caputo, Fanny Mameli, Marta Sienkiewicz, Andrzej Licoccia, Silvia Stellacci, Francesco Ghibelli, Lina Traversa, Enrico A novel synthetic approach of cerium oxide nanoparticles with improved biomedical activity |
title | A novel synthetic approach of cerium oxide nanoparticles with improved biomedical activity |
title_full | A novel synthetic approach of cerium oxide nanoparticles with improved biomedical activity |
title_fullStr | A novel synthetic approach of cerium oxide nanoparticles with improved biomedical activity |
title_full_unstemmed | A novel synthetic approach of cerium oxide nanoparticles with improved biomedical activity |
title_short | A novel synthetic approach of cerium oxide nanoparticles with improved biomedical activity |
title_sort | novel synthetic approach of cerium oxide nanoparticles with improved biomedical activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5498533/ https://www.ncbi.nlm.nih.gov/pubmed/28680107 http://dx.doi.org/10.1038/s41598-017-04098-6 |
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