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Silica/quercetin sol–gel hybrids as antioxidant dental implant materials

The development of biomaterials with intrinsic antioxidant properties could represent a valuable strategy for preventing the onset of peri-implant diseases. In this context, quercetin, a naturally occurring flavonoid, has been entrapped at different weight percentages in a silica-based inorganic mat...

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Autores principales: Catauro, Michelina, Papale, Ferdinando, Bollino, Flavia, Piccolella, Simona, Marciano, Sabina, Nocera, Paola, Pacifico, Severina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5099839/
https://www.ncbi.nlm.nih.gov/pubmed/27877802
http://dx.doi.org/10.1088/1468-6996/16/3/035001
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author Catauro, Michelina
Papale, Ferdinando
Bollino, Flavia
Piccolella, Simona
Marciano, Sabina
Nocera, Paola
Pacifico, Severina
author_facet Catauro, Michelina
Papale, Ferdinando
Bollino, Flavia
Piccolella, Simona
Marciano, Sabina
Nocera, Paola
Pacifico, Severina
author_sort Catauro, Michelina
collection PubMed
description The development of biomaterials with intrinsic antioxidant properties could represent a valuable strategy for preventing the onset of peri-implant diseases. In this context, quercetin, a naturally occurring flavonoid, has been entrapped at different weight percentages in a silica-based inorganic material by a sol–gel route. The establishment of hydrogen bond interactions between the flavonol and the solid matrix was ascertained by Fourier transform infrared spectroscopy. This technique also evidenced changes in the stretching frequencies of the quercetin dienonic moiety, suggesting that the formation of a secondary product occurs. Scanning electron microscopy was applied to detect the morphology of the synthesized materials. Their bioactivity was shown by the formation of a hydroxyapatite layer on sample surface soaked in a fluid that simulates the composition of human blood plasma. When the potential release of flavonol was determined by liquid chromatography coupled with ultraviolet and electrospray ionization tandem mass spectrometry techniques, the eluates displayed a retention time that was 0.5 min less than quercetin. Collision-activated dissociation mass spectrometry and untraviolet-visible spectroscopy were in accordance with the release of a quercetin derivative. The antiradical properties of the investigated systems were evaluated by DPPH and ABTS methods, whereas the 2,7-dichlorofluorescein diacetate assay highlighted their ability to inhibit the H(2)O(2)-induced intracellular production of reactive oxygen species in NIH-3T3 mouse fibroblast cells. Data obtained, along with data gathered from the MTT cytotoxicity test, revealed that the materials that entrapped the highest amount of quercetin showed notable antioxidant effectiveness.
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spelling pubmed-50998392016-11-22 Silica/quercetin sol–gel hybrids as antioxidant dental implant materials Catauro, Michelina Papale, Ferdinando Bollino, Flavia Piccolella, Simona Marciano, Sabina Nocera, Paola Pacifico, Severina Sci Technol Adv Mater Papers The development of biomaterials with intrinsic antioxidant properties could represent a valuable strategy for preventing the onset of peri-implant diseases. In this context, quercetin, a naturally occurring flavonoid, has been entrapped at different weight percentages in a silica-based inorganic material by a sol–gel route. The establishment of hydrogen bond interactions between the flavonol and the solid matrix was ascertained by Fourier transform infrared spectroscopy. This technique also evidenced changes in the stretching frequencies of the quercetin dienonic moiety, suggesting that the formation of a secondary product occurs. Scanning electron microscopy was applied to detect the morphology of the synthesized materials. Their bioactivity was shown by the formation of a hydroxyapatite layer on sample surface soaked in a fluid that simulates the composition of human blood plasma. When the potential release of flavonol was determined by liquid chromatography coupled with ultraviolet and electrospray ionization tandem mass spectrometry techniques, the eluates displayed a retention time that was 0.5 min less than quercetin. Collision-activated dissociation mass spectrometry and untraviolet-visible spectroscopy were in accordance with the release of a quercetin derivative. The antiradical properties of the investigated systems were evaluated by DPPH and ABTS methods, whereas the 2,7-dichlorofluorescein diacetate assay highlighted their ability to inhibit the H(2)O(2)-induced intracellular production of reactive oxygen species in NIH-3T3 mouse fibroblast cells. Data obtained, along with data gathered from the MTT cytotoxicity test, revealed that the materials that entrapped the highest amount of quercetin showed notable antioxidant effectiveness. Taylor & Francis 2015-05-05 /pmc/articles/PMC5099839/ /pubmed/27877802 http://dx.doi.org/10.1088/1468-6996/16/3/035001 Text en © 2015 National Institute for Materials Science http://creativecommons.org/licenses/by/3.0/ Content from this work may be used under the terms of the Creative Commons Attribution 3.0 licence (http://creativecommons.org/licenses/by/3.0) . Any further distribution of this work must maintain attribution to the author(s) and the title of the work, journal citation and DOI.
spellingShingle Papers
Catauro, Michelina
Papale, Ferdinando
Bollino, Flavia
Piccolella, Simona
Marciano, Sabina
Nocera, Paola
Pacifico, Severina
Silica/quercetin sol–gel hybrids as antioxidant dental implant materials
title Silica/quercetin sol–gel hybrids as antioxidant dental implant materials
title_full Silica/quercetin sol–gel hybrids as antioxidant dental implant materials
title_fullStr Silica/quercetin sol–gel hybrids as antioxidant dental implant materials
title_full_unstemmed Silica/quercetin sol–gel hybrids as antioxidant dental implant materials
title_short Silica/quercetin sol–gel hybrids as antioxidant dental implant materials
title_sort silica/quercetin sol–gel hybrids as antioxidant dental implant materials
topic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5099839/
https://www.ncbi.nlm.nih.gov/pubmed/27877802
http://dx.doi.org/10.1088/1468-6996/16/3/035001
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