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Development of Chitosan/Silver Sulfadiazine/Zeolite Composite Films for Wound Dressing

Biopolymeric films with silver sulfadiazine (AgSD) are proposed as an alternative to the occlusive AgSD-containing creams and gauzes, which are commonly used in the treatment of conventional burns. While the recognized cytotoxicity of AgSD has been reported to compromise its use as an antimicrobial...

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Autores principales: Hissae Yassue-Cordeiro, Patricia, Henrique Zandonai, Cássio, Pereira Genesi, Bianca, Santos Lopes, Patrícia, Sanchez-Lopez, Elena, Luisa Garcia, Maria, Regina Camargo Fernandes-Machado, Nádia, Severino, Patrícia, B. Souto, Eliana, Ferreira da Silva, Classius
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835377/
https://www.ncbi.nlm.nih.gov/pubmed/31615120
http://dx.doi.org/10.3390/pharmaceutics11100535
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author Hissae Yassue-Cordeiro, Patricia
Henrique Zandonai, Cássio
Pereira Genesi, Bianca
Santos Lopes, Patrícia
Sanchez-Lopez, Elena
Luisa Garcia, Maria
Regina Camargo Fernandes-Machado, Nádia
Severino, Patrícia
B. Souto, Eliana
Ferreira da Silva, Classius
author_facet Hissae Yassue-Cordeiro, Patricia
Henrique Zandonai, Cássio
Pereira Genesi, Bianca
Santos Lopes, Patrícia
Sanchez-Lopez, Elena
Luisa Garcia, Maria
Regina Camargo Fernandes-Machado, Nádia
Severino, Patrícia
B. Souto, Eliana
Ferreira da Silva, Classius
author_sort Hissae Yassue-Cordeiro, Patricia
collection PubMed
description Biopolymeric films with silver sulfadiazine (AgSD) are proposed as an alternative to the occlusive AgSD-containing creams and gauzes, which are commonly used in the treatment of conventional burns. While the recognized cytotoxicity of AgSD has been reported to compromise its use as an antimicrobial drug in pharmaceuticals, this limitation can be overcome by developing sustained-release formulations. Microporous materials as zeolites can be used as drug delivery systems for sustained release of AgSD. The purpose of this work was the development and characterization of chitosan/zeolite composite films to be used as wound dressings. Zeolite was impregnated with AgSD before the production of the composite films. The physicochemical properties of zeolites and the films were evaluated, as well as the antimicrobial activity of the polymeric films and the cytotoxicity of the films in fibroblasts Balb 3T3/c. Impregnated zeolite exhibited changes in FTIR spectra and XRD diffraction patterns, in comparison to non-impregnated composites, which corroborate the results obtained with EDX-SEM. The pure chitosan film was compact and without noticeable defects and macropores, while the film with zeolite was opaquer, more rigid, and efficient against Candida albicans and some gram-negative bacteria. The safety evaluation showed that although the AgSD films present cytotoxicity, they could be used in a concentration-dependent fashion.
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spelling pubmed-68353772019-11-25 Development of Chitosan/Silver Sulfadiazine/Zeolite Composite Films for Wound Dressing Hissae Yassue-Cordeiro, Patricia Henrique Zandonai, Cássio Pereira Genesi, Bianca Santos Lopes, Patrícia Sanchez-Lopez, Elena Luisa Garcia, Maria Regina Camargo Fernandes-Machado, Nádia Severino, Patrícia B. Souto, Eliana Ferreira da Silva, Classius Pharmaceutics Article Biopolymeric films with silver sulfadiazine (AgSD) are proposed as an alternative to the occlusive AgSD-containing creams and gauzes, which are commonly used in the treatment of conventional burns. While the recognized cytotoxicity of AgSD has been reported to compromise its use as an antimicrobial drug in pharmaceuticals, this limitation can be overcome by developing sustained-release formulations. Microporous materials as zeolites can be used as drug delivery systems for sustained release of AgSD. The purpose of this work was the development and characterization of chitosan/zeolite composite films to be used as wound dressings. Zeolite was impregnated with AgSD before the production of the composite films. The physicochemical properties of zeolites and the films were evaluated, as well as the antimicrobial activity of the polymeric films and the cytotoxicity of the films in fibroblasts Balb 3T3/c. Impregnated zeolite exhibited changes in FTIR spectra and XRD diffraction patterns, in comparison to non-impregnated composites, which corroborate the results obtained with EDX-SEM. The pure chitosan film was compact and without noticeable defects and macropores, while the film with zeolite was opaquer, more rigid, and efficient against Candida albicans and some gram-negative bacteria. The safety evaluation showed that although the AgSD films present cytotoxicity, they could be used in a concentration-dependent fashion. MDPI 2019-10-14 /pmc/articles/PMC6835377/ /pubmed/31615120 http://dx.doi.org/10.3390/pharmaceutics11100535 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Hissae Yassue-Cordeiro, Patricia
Henrique Zandonai, Cássio
Pereira Genesi, Bianca
Santos Lopes, Patrícia
Sanchez-Lopez, Elena
Luisa Garcia, Maria
Regina Camargo Fernandes-Machado, Nádia
Severino, Patrícia
B. Souto, Eliana
Ferreira da Silva, Classius
Development of Chitosan/Silver Sulfadiazine/Zeolite Composite Films for Wound Dressing
title Development of Chitosan/Silver Sulfadiazine/Zeolite Composite Films for Wound Dressing
title_full Development of Chitosan/Silver Sulfadiazine/Zeolite Composite Films for Wound Dressing
title_fullStr Development of Chitosan/Silver Sulfadiazine/Zeolite Composite Films for Wound Dressing
title_full_unstemmed Development of Chitosan/Silver Sulfadiazine/Zeolite Composite Films for Wound Dressing
title_short Development of Chitosan/Silver Sulfadiazine/Zeolite Composite Films for Wound Dressing
title_sort development of chitosan/silver sulfadiazine/zeolite composite films for wound dressing
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6835377/
https://www.ncbi.nlm.nih.gov/pubmed/31615120
http://dx.doi.org/10.3390/pharmaceutics11100535
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