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Bilayer Mucoadhesive Buccal Film for Mucosal Ulcers Treatment: Development, Characterization, and Single Study Case

The formation of mucosal ulcers is an end result of epithelial damage, and it occurs due to some specific causes, such as trauma, aphthous stomatitis, lichen planus and lichenoid reactions, cytotoxic effects of chemotherapy and radiation, and drug-induced hypersensitivity reactions and malignant set...

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Autores principales: Alves, Thais F. R., Rios, Alesssandra C., da Silva Pontes, Katiusca, Portella, Decio L., Aranha, Norberto, Severino, Patricia, Souto, Eliana B., Gonsalves, Joyce K. M., de Souza Nunes, Rogeria, Chaud, Marco V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408552/
https://www.ncbi.nlm.nih.gov/pubmed/32664574
http://dx.doi.org/10.3390/pharmaceutics12070657
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author Alves, Thais F. R.
Rios, Alesssandra C.
da Silva Pontes, Katiusca
Portella, Decio L.
Aranha, Norberto
Severino, Patricia
Souto, Eliana B.
Gonsalves, Joyce K. M.
de Souza Nunes, Rogeria
Chaud, Marco V.
author_facet Alves, Thais F. R.
Rios, Alesssandra C.
da Silva Pontes, Katiusca
Portella, Decio L.
Aranha, Norberto
Severino, Patricia
Souto, Eliana B.
Gonsalves, Joyce K. M.
de Souza Nunes, Rogeria
Chaud, Marco V.
author_sort Alves, Thais F. R.
collection PubMed
description The formation of mucosal ulcers is an end result of epithelial damage, and it occurs due to some specific causes, such as trauma, aphthous stomatitis, lichen planus and lichenoid reactions, cytotoxic effects of chemotherapy and radiation, and drug-induced hypersensitivity reactions and malignant settings. This study focused on films for target drug delivery with respect to the treatment of the diseases of the oral mucosa, specifically mucositis. The results of a single clinical study as a pre-experimental design was performed and followed up to the outcome until 30 days. The polymeric film was prepared in a mucoadhesive bilayer structure: the basal layer with lidocaine HCl had a faster release than the apical layer with benzydamine HCl and N-acetyl-cysteine. Fourier Transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC), and SEM characterized the physical–chemical and morphological properties. The cell viability and cytotoxicity were evaluated in cell line MCF7. The transport mechanism of the solvent (swelling) and the drugs in the basal or apical layer (drug release) was explained with mathematical models. To evaluate the effect of movement inside the mouth, the folding endurance was determined. The mucoadhesive bilayer film is biologically safe and stimulates cellular proliferation. A single study in vivo demonstrated the therapeutic effect of the mucoadhesive bilayer film in buccal mucositis.
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spelling pubmed-74085522020-08-13 Bilayer Mucoadhesive Buccal Film for Mucosal Ulcers Treatment: Development, Characterization, and Single Study Case Alves, Thais F. R. Rios, Alesssandra C. da Silva Pontes, Katiusca Portella, Decio L. Aranha, Norberto Severino, Patricia Souto, Eliana B. Gonsalves, Joyce K. M. de Souza Nunes, Rogeria Chaud, Marco V. Pharmaceutics Article The formation of mucosal ulcers is an end result of epithelial damage, and it occurs due to some specific causes, such as trauma, aphthous stomatitis, lichen planus and lichenoid reactions, cytotoxic effects of chemotherapy and radiation, and drug-induced hypersensitivity reactions and malignant settings. This study focused on films for target drug delivery with respect to the treatment of the diseases of the oral mucosa, specifically mucositis. The results of a single clinical study as a pre-experimental design was performed and followed up to the outcome until 30 days. The polymeric film was prepared in a mucoadhesive bilayer structure: the basal layer with lidocaine HCl had a faster release than the apical layer with benzydamine HCl and N-acetyl-cysteine. Fourier Transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC), and SEM characterized the physical–chemical and morphological properties. The cell viability and cytotoxicity were evaluated in cell line MCF7. The transport mechanism of the solvent (swelling) and the drugs in the basal or apical layer (drug release) was explained with mathematical models. To evaluate the effect of movement inside the mouth, the folding endurance was determined. The mucoadhesive bilayer film is biologically safe and stimulates cellular proliferation. A single study in vivo demonstrated the therapeutic effect of the mucoadhesive bilayer film in buccal mucositis. MDPI 2020-07-11 /pmc/articles/PMC7408552/ /pubmed/32664574 http://dx.doi.org/10.3390/pharmaceutics12070657 Text en © 2020 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
Alves, Thais F. R.
Rios, Alesssandra C.
da Silva Pontes, Katiusca
Portella, Decio L.
Aranha, Norberto
Severino, Patricia
Souto, Eliana B.
Gonsalves, Joyce K. M.
de Souza Nunes, Rogeria
Chaud, Marco V.
Bilayer Mucoadhesive Buccal Film for Mucosal Ulcers Treatment: Development, Characterization, and Single Study Case
title Bilayer Mucoadhesive Buccal Film for Mucosal Ulcers Treatment: Development, Characterization, and Single Study Case
title_full Bilayer Mucoadhesive Buccal Film for Mucosal Ulcers Treatment: Development, Characterization, and Single Study Case
title_fullStr Bilayer Mucoadhesive Buccal Film for Mucosal Ulcers Treatment: Development, Characterization, and Single Study Case
title_full_unstemmed Bilayer Mucoadhesive Buccal Film for Mucosal Ulcers Treatment: Development, Characterization, and Single Study Case
title_short Bilayer Mucoadhesive Buccal Film for Mucosal Ulcers Treatment: Development, Characterization, and Single Study Case
title_sort bilayer mucoadhesive buccal film for mucosal ulcers treatment: development, characterization, and single study case
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7408552/
https://www.ncbi.nlm.nih.gov/pubmed/32664574
http://dx.doi.org/10.3390/pharmaceutics12070657
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