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Colon-Specific Drug Delivery Behavior of pH-Responsive PMAA/Perlite Composite
The preparation, characterization, and in vitro release of 5-aminosalicylic acid (5-ASA) from methacrylic acid (MAA)/perlite composites (APC) prepared via a sol–gel route are reported. The free-radical graft polymerization of methacrylic acid (MAA) onto perlite particles was studied experimentally....
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Formato: | Texto |
Lenguaje: | English |
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Molecular Diversity Preservation International (MDPI)
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2871130/ https://www.ncbi.nlm.nih.gov/pubmed/20480034 http://dx.doi.org/10.3390/ijms11041546 |
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author | Mahkam, Mehrdad Vakhshouri, Laleh |
author_facet | Mahkam, Mehrdad Vakhshouri, Laleh |
author_sort | Mahkam, Mehrdad |
collection | PubMed |
description | The preparation, characterization, and in vitro release of 5-aminosalicylic acid (5-ASA) from methacrylic acid (MAA)/perlite composites (APC) prepared via a sol–gel route are reported. The free-radical graft polymerization of methacrylic acid (MAA) onto perlite particles was studied experimentally. The grafting procedure consisted of surface activation with 3-(trimethoxysilyl) propyl methacrylate (TSPA), followed by free-radical graft polymerization of methacrylic acid (MAA) in ethyl acetate with 2,2′-azobisisobutyronitrile (AIBN) initiator. The composition of the composites hybrid materials was determined by FTIR spectroscopy. Equilibrium swelling studies were carried out in enzyme-free simulated gastric and intestinal fluids (SGF and SIF, respectively). The dried composites were immersed in a saturated solution of 5-ASA in water overnight and dried over a period of three days at room temperature and the in vitro release profiles were established separately in both (SGF, pH 1) and (SIF, pH 7.4). The 5-ASA concentration of the solution was measured using a UV-Vis spectrophotometer (205 nm) at different time intervals. The in vitro drug release test revealed that the release rate of 5-ASA in buffer solutions increased with the silica content in the composites; on the contrary, the increase of the content of 3-(trimethoxysilyl)propyl methacrylate (TSPA), a coupling agent, decreased the drug release rate. |
format | Text |
id | pubmed-2871130 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-28711302010-05-17 Colon-Specific Drug Delivery Behavior of pH-Responsive PMAA/Perlite Composite Mahkam, Mehrdad Vakhshouri, Laleh Int J Mol Sci Article The preparation, characterization, and in vitro release of 5-aminosalicylic acid (5-ASA) from methacrylic acid (MAA)/perlite composites (APC) prepared via a sol–gel route are reported. The free-radical graft polymerization of methacrylic acid (MAA) onto perlite particles was studied experimentally. The grafting procedure consisted of surface activation with 3-(trimethoxysilyl) propyl methacrylate (TSPA), followed by free-radical graft polymerization of methacrylic acid (MAA) in ethyl acetate with 2,2′-azobisisobutyronitrile (AIBN) initiator. The composition of the composites hybrid materials was determined by FTIR spectroscopy. Equilibrium swelling studies were carried out in enzyme-free simulated gastric and intestinal fluids (SGF and SIF, respectively). The dried composites were immersed in a saturated solution of 5-ASA in water overnight and dried over a period of three days at room temperature and the in vitro release profiles were established separately in both (SGF, pH 1) and (SIF, pH 7.4). The 5-ASA concentration of the solution was measured using a UV-Vis spectrophotometer (205 nm) at different time intervals. The in vitro drug release test revealed that the release rate of 5-ASA in buffer solutions increased with the silica content in the composites; on the contrary, the increase of the content of 3-(trimethoxysilyl)propyl methacrylate (TSPA), a coupling agent, decreased the drug release rate. Molecular Diversity Preservation International (MDPI) 2010-04-12 /pmc/articles/PMC2871130/ /pubmed/20480034 http://dx.doi.org/10.3390/ijms11041546 Text en © 2010 by the authors; licensee Molecular Diversity Preservation International, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Mahkam, Mehrdad Vakhshouri, Laleh Colon-Specific Drug Delivery Behavior of pH-Responsive PMAA/Perlite Composite |
title | Colon-Specific Drug Delivery Behavior of pH-Responsive PMAA/Perlite Composite |
title_full | Colon-Specific Drug Delivery Behavior of pH-Responsive PMAA/Perlite Composite |
title_fullStr | Colon-Specific Drug Delivery Behavior of pH-Responsive PMAA/Perlite Composite |
title_full_unstemmed | Colon-Specific Drug Delivery Behavior of pH-Responsive PMAA/Perlite Composite |
title_short | Colon-Specific Drug Delivery Behavior of pH-Responsive PMAA/Perlite Composite |
title_sort | colon-specific drug delivery behavior of ph-responsive pmaa/perlite composite |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2871130/ https://www.ncbi.nlm.nih.gov/pubmed/20480034 http://dx.doi.org/10.3390/ijms11041546 |
work_keys_str_mv | AT mahkammehrdad colonspecificdrugdeliverybehaviorofphresponsivepmaaperlitecomposite AT vakhshourilaleh colonspecificdrugdeliverybehaviorofphresponsivepmaaperlitecomposite |