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Physicochemical Characterization and Drug Release Properties of Methyl-Substituted Silica Xerogels Made Using Sol–Gel Process

In this work, a multi-analytical approach involving nitrogen porosimetry, small angle neutron and X-ray scattering, Fourier transform infrared (FTIR) and nuclear magnetic resonance (NMR) spectroscopies, X-ray diffraction, thermal analysis and electron microscopy was applied to organically modified s...

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Autores principales: Len, Adél, Paladini, Giuseppe, Románszki, Loránd, Putz, Ana-Maria, Almásy, László, László, Krisztina, Bálint, Szabolcs, Krajnc, Andraž, Kriechbaum, Manfred, Kuncser, Andrei, Kalmár, József, Dudás, Zoltán
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8430635/
https://www.ncbi.nlm.nih.gov/pubmed/34502104
http://dx.doi.org/10.3390/ijms22179197
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author Len, Adél
Paladini, Giuseppe
Románszki, Loránd
Putz, Ana-Maria
Almásy, László
László, Krisztina
Bálint, Szabolcs
Krajnc, Andraž
Kriechbaum, Manfred
Kuncser, Andrei
Kalmár, József
Dudás, Zoltán
author_facet Len, Adél
Paladini, Giuseppe
Románszki, Loránd
Putz, Ana-Maria
Almásy, László
László, Krisztina
Bálint, Szabolcs
Krajnc, Andraž
Kriechbaum, Manfred
Kuncser, Andrei
Kalmár, József
Dudás, Zoltán
author_sort Len, Adél
collection PubMed
description In this work, a multi-analytical approach involving nitrogen porosimetry, small angle neutron and X-ray scattering, Fourier transform infrared (FTIR) and nuclear magnetic resonance (NMR) spectroscopies, X-ray diffraction, thermal analysis and electron microscopy was applied to organically modified silica-based xerogels obtained through the sol–gel process. Starting from a tetraethoxysilane (TEOS) precursor, methyltriethoxysilane (MTES) was added to the reaction mixture at two different pH values (2.0 and 4.5) producing hybrid xerogels with different TEOS/MTES molar ratios. Significant differences in the structure were revealed in terms of the chemical composition of the silica network, hydrophilic/hydrophobic profile, particle dimension, pore shape/size and surface characteristics. The combined use of structural characterization methods allowed us to reveal a relation between the cavity dimensions, the synthesis pH value and the grade of methyl substitution. The effect of the structural properties on the controlled Captopril release efficiency has also been tested. This knowledge facilitates tailoring the pore network for specific usage in biological/medical applications. Knowledge on structural aspects, as reported in this work, represents a key starting point for the production of high-performance silica-based hybrid materials showing enhanced efficacy compared to bare silica prepared using only TEOS.
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spelling pubmed-84306352021-09-11 Physicochemical Characterization and Drug Release Properties of Methyl-Substituted Silica Xerogels Made Using Sol–Gel Process Len, Adél Paladini, Giuseppe Románszki, Loránd Putz, Ana-Maria Almásy, László László, Krisztina Bálint, Szabolcs Krajnc, Andraž Kriechbaum, Manfred Kuncser, Andrei Kalmár, József Dudás, Zoltán Int J Mol Sci Article In this work, a multi-analytical approach involving nitrogen porosimetry, small angle neutron and X-ray scattering, Fourier transform infrared (FTIR) and nuclear magnetic resonance (NMR) spectroscopies, X-ray diffraction, thermal analysis and electron microscopy was applied to organically modified silica-based xerogels obtained through the sol–gel process. Starting from a tetraethoxysilane (TEOS) precursor, methyltriethoxysilane (MTES) was added to the reaction mixture at two different pH values (2.0 and 4.5) producing hybrid xerogels with different TEOS/MTES molar ratios. Significant differences in the structure were revealed in terms of the chemical composition of the silica network, hydrophilic/hydrophobic profile, particle dimension, pore shape/size and surface characteristics. The combined use of structural characterization methods allowed us to reveal a relation between the cavity dimensions, the synthesis pH value and the grade of methyl substitution. The effect of the structural properties on the controlled Captopril release efficiency has also been tested. This knowledge facilitates tailoring the pore network for specific usage in biological/medical applications. Knowledge on structural aspects, as reported in this work, represents a key starting point for the production of high-performance silica-based hybrid materials showing enhanced efficacy compared to bare silica prepared using only TEOS. MDPI 2021-08-25 /pmc/articles/PMC8430635/ /pubmed/34502104 http://dx.doi.org/10.3390/ijms22179197 Text en © 2021 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
Len, Adél
Paladini, Giuseppe
Románszki, Loránd
Putz, Ana-Maria
Almásy, László
László, Krisztina
Bálint, Szabolcs
Krajnc, Andraž
Kriechbaum, Manfred
Kuncser, Andrei
Kalmár, József
Dudás, Zoltán
Physicochemical Characterization and Drug Release Properties of Methyl-Substituted Silica Xerogels Made Using Sol–Gel Process
title Physicochemical Characterization and Drug Release Properties of Methyl-Substituted Silica Xerogels Made Using Sol–Gel Process
title_full Physicochemical Characterization and Drug Release Properties of Methyl-Substituted Silica Xerogels Made Using Sol–Gel Process
title_fullStr Physicochemical Characterization and Drug Release Properties of Methyl-Substituted Silica Xerogels Made Using Sol–Gel Process
title_full_unstemmed Physicochemical Characterization and Drug Release Properties of Methyl-Substituted Silica Xerogels Made Using Sol–Gel Process
title_short Physicochemical Characterization and Drug Release Properties of Methyl-Substituted Silica Xerogels Made Using Sol–Gel Process
title_sort physicochemical characterization and drug release properties of methyl-substituted silica xerogels made using sol–gel process
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8430635/
https://www.ncbi.nlm.nih.gov/pubmed/34502104
http://dx.doi.org/10.3390/ijms22179197
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