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Chitosan-Based Composite Membranes with Different Biocompatible Metal Oxide Nanoparticles: Physicochemical Properties and Drug-Release Study

Chitosan (CS) composite membranes were prepared using different biocompatible metal oxide nanoparticles (NPs): titanium dioxide (TiO(2)); iron oxide (Fe(3)O(4)); and aluminum oxide (Al(2)O(3)). For each nanoparticle, the CS-based composite membranes were prepared with two NPs contents in the CS solu...

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Autores principales: Baroudi, Alia, García-Payo, Carmen, Khayet, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10347105/
https://www.ncbi.nlm.nih.gov/pubmed/37447450
http://dx.doi.org/10.3390/polym15132804
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author Baroudi, Alia
García-Payo, Carmen
Khayet, Mohamed
author_facet Baroudi, Alia
García-Payo, Carmen
Khayet, Mohamed
author_sort Baroudi, Alia
collection PubMed
description Chitosan (CS) composite membranes were prepared using different biocompatible metal oxide nanoparticles (NPs): titanium dioxide (TiO(2)); iron oxide (Fe(3)O(4)); and aluminum oxide (Al(2)O(3)). For each nanoparticle, the CS-based composite membranes were prepared with two NPs contents in the CS solution, high (H) and low (L) NPs concentrations. To establish both concentrations, the NPs saturation point in the CS polymeric matrix was determined. The influence of NP concentrations on the physicochemical properties of the CS films was assessed. The prepared CS membranes were characterized with different techniques, such as X-ray diffraction (XRD), scanning electron microscopy (SEM), and zeta potential. It was found that the addition of NPs in the CS matrix improved both swelling and mechanical properties. Nanocomposite CS membranes could be prepared using Al(2)O(3) NPs. Swelling experiments revealed different pH-sensitive mechanisms, which might be beneficial in biomedical applications since solute permeation through CS-based composite membranes could be controlled by adjusting environmental conditions. When aspirin transport (ASA) through the prepared membranes was carried out in different release media, SGF (simulating gastric fluid) and SIF (simulating intestinal fluid without enzymes), it was observed that the Fickian diffusion coefficient (D) was conditioned by the pH of the release solution. In SGIT (simulating gastrointestinal transit) medium, a transition time (t(trans)) was detected due to the shrinkage of the CS polymeric chains, and the drug release depended not only on the Fickian’s diffusion but also on the shrinkage of the biopolymer, obeying Peppas and Sahlin equation.
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spelling pubmed-103471052023-07-15 Chitosan-Based Composite Membranes with Different Biocompatible Metal Oxide Nanoparticles: Physicochemical Properties and Drug-Release Study Baroudi, Alia García-Payo, Carmen Khayet, Mohamed Polymers (Basel) Article Chitosan (CS) composite membranes were prepared using different biocompatible metal oxide nanoparticles (NPs): titanium dioxide (TiO(2)); iron oxide (Fe(3)O(4)); and aluminum oxide (Al(2)O(3)). For each nanoparticle, the CS-based composite membranes were prepared with two NPs contents in the CS solution, high (H) and low (L) NPs concentrations. To establish both concentrations, the NPs saturation point in the CS polymeric matrix was determined. The influence of NP concentrations on the physicochemical properties of the CS films was assessed. The prepared CS membranes were characterized with different techniques, such as X-ray diffraction (XRD), scanning electron microscopy (SEM), and zeta potential. It was found that the addition of NPs in the CS matrix improved both swelling and mechanical properties. Nanocomposite CS membranes could be prepared using Al(2)O(3) NPs. Swelling experiments revealed different pH-sensitive mechanisms, which might be beneficial in biomedical applications since solute permeation through CS-based composite membranes could be controlled by adjusting environmental conditions. When aspirin transport (ASA) through the prepared membranes was carried out in different release media, SGF (simulating gastric fluid) and SIF (simulating intestinal fluid without enzymes), it was observed that the Fickian diffusion coefficient (D) was conditioned by the pH of the release solution. In SGIT (simulating gastrointestinal transit) medium, a transition time (t(trans)) was detected due to the shrinkage of the CS polymeric chains, and the drug release depended not only on the Fickian’s diffusion but also on the shrinkage of the biopolymer, obeying Peppas and Sahlin equation. MDPI 2023-06-24 /pmc/articles/PMC10347105/ /pubmed/37447450 http://dx.doi.org/10.3390/polym15132804 Text en © 2023 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
Baroudi, Alia
García-Payo, Carmen
Khayet, Mohamed
Chitosan-Based Composite Membranes with Different Biocompatible Metal Oxide Nanoparticles: Physicochemical Properties and Drug-Release Study
title Chitosan-Based Composite Membranes with Different Biocompatible Metal Oxide Nanoparticles: Physicochemical Properties and Drug-Release Study
title_full Chitosan-Based Composite Membranes with Different Biocompatible Metal Oxide Nanoparticles: Physicochemical Properties and Drug-Release Study
title_fullStr Chitosan-Based Composite Membranes with Different Biocompatible Metal Oxide Nanoparticles: Physicochemical Properties and Drug-Release Study
title_full_unstemmed Chitosan-Based Composite Membranes with Different Biocompatible Metal Oxide Nanoparticles: Physicochemical Properties and Drug-Release Study
title_short Chitosan-Based Composite Membranes with Different Biocompatible Metal Oxide Nanoparticles: Physicochemical Properties and Drug-Release Study
title_sort chitosan-based composite membranes with different biocompatible metal oxide nanoparticles: physicochemical properties and drug-release study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10347105/
https://www.ncbi.nlm.nih.gov/pubmed/37447450
http://dx.doi.org/10.3390/polym15132804
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