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Tablet of Ximenia Americana L. Developed from Mucoadhesive Polymers for Future Use in Oral Treatment of Fungal Infections

The use of biocompatible polymers such as Hydroxypropylmethylcellulose (HPMC), Hydroxyethylcellulose (HEC), Carboxymethylcellulose (CMC), and Carbopol in solid formulations results in mucoadhesive systems capable of promoting the prolonged and localized release of Active Pharmaceutical Ingredients (...

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Autores principales: Almeida, Lucas, Júnior, João Augusto Oshiro, Silva, Milena, Nóbrega, Fernanda, Andrade, Jéssica, Santos, Widson, Ribeiro, Angélica, Conceição, Marta, Veras, Germano, Medeiros, Ana Cláudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419192/
https://www.ncbi.nlm.nih.gov/pubmed/30960363
http://dx.doi.org/10.3390/polym11020379
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author Almeida, Lucas
Júnior, João Augusto Oshiro
Silva, Milena
Nóbrega, Fernanda
Andrade, Jéssica
Santos, Widson
Ribeiro, Angélica
Conceição, Marta
Veras, Germano
Medeiros, Ana Cláudia
author_facet Almeida, Lucas
Júnior, João Augusto Oshiro
Silva, Milena
Nóbrega, Fernanda
Andrade, Jéssica
Santos, Widson
Ribeiro, Angélica
Conceição, Marta
Veras, Germano
Medeiros, Ana Cláudia
author_sort Almeida, Lucas
collection PubMed
description The use of biocompatible polymers such as Hydroxypropylmethylcellulose (HPMC), Hydroxyethylcellulose (HEC), Carboxymethylcellulose (CMC), and Carbopol in solid formulations results in mucoadhesive systems capable of promoting the prolonged and localized release of Active Pharmaceutical Ingredients (APIs). This strategy represents a technological innovation that can be applied to improving the treatment of oral infections, such as oral candidiasis. Therefore, the aim of this study was to develop a tablet of Ximenia americana L. from mucoadhesive polymers for use in the treatment of oral candidiasis. An X. americana extract (MIC of 125 μg·mL(−1)) was obtained by turbolysis at 50% of ethanol, a level that demonstrated activity against Candida albicans. Differential Thermal Analysis and Fourier Transform Infrared Spectroscopy techniques allowed the choice of HPMC as a mucoadhesive agent, besides polyvinylpyrrolidone, magnesium stearate, and mannitol to integrate the formulation of X. americana. These excipients were granulated with an ethanolic solution 70% v/v at PVP 5%, and a mucoadhesive tablet was obtained by compression. Finally, mucoadhesive strength was evaluated, and the results demonstrated good mucoadhesive forces in mucin disk and pig buccal mucosa. Therefore, the study allowed a new alternative to be developed for the treatment of buccal candidiasis, one which overcomes the inconveniences of common treatments, costs little, and facilitates patients’ adhesion.
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spelling pubmed-64191922019-04-02 Tablet of Ximenia Americana L. Developed from Mucoadhesive Polymers for Future Use in Oral Treatment of Fungal Infections Almeida, Lucas Júnior, João Augusto Oshiro Silva, Milena Nóbrega, Fernanda Andrade, Jéssica Santos, Widson Ribeiro, Angélica Conceição, Marta Veras, Germano Medeiros, Ana Cláudia Polymers (Basel) Article The use of biocompatible polymers such as Hydroxypropylmethylcellulose (HPMC), Hydroxyethylcellulose (HEC), Carboxymethylcellulose (CMC), and Carbopol in solid formulations results in mucoadhesive systems capable of promoting the prolonged and localized release of Active Pharmaceutical Ingredients (APIs). This strategy represents a technological innovation that can be applied to improving the treatment of oral infections, such as oral candidiasis. Therefore, the aim of this study was to develop a tablet of Ximenia americana L. from mucoadhesive polymers for use in the treatment of oral candidiasis. An X. americana extract (MIC of 125 μg·mL(−1)) was obtained by turbolysis at 50% of ethanol, a level that demonstrated activity against Candida albicans. Differential Thermal Analysis and Fourier Transform Infrared Spectroscopy techniques allowed the choice of HPMC as a mucoadhesive agent, besides polyvinylpyrrolidone, magnesium stearate, and mannitol to integrate the formulation of X. americana. These excipients were granulated with an ethanolic solution 70% v/v at PVP 5%, and a mucoadhesive tablet was obtained by compression. Finally, mucoadhesive strength was evaluated, and the results demonstrated good mucoadhesive forces in mucin disk and pig buccal mucosa. Therefore, the study allowed a new alternative to be developed for the treatment of buccal candidiasis, one which overcomes the inconveniences of common treatments, costs little, and facilitates patients’ adhesion. MDPI 2019-02-20 /pmc/articles/PMC6419192/ /pubmed/30960363 http://dx.doi.org/10.3390/polym11020379 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
Almeida, Lucas
Júnior, João Augusto Oshiro
Silva, Milena
Nóbrega, Fernanda
Andrade, Jéssica
Santos, Widson
Ribeiro, Angélica
Conceição, Marta
Veras, Germano
Medeiros, Ana Cláudia
Tablet of Ximenia Americana L. Developed from Mucoadhesive Polymers for Future Use in Oral Treatment of Fungal Infections
title Tablet of Ximenia Americana L. Developed from Mucoadhesive Polymers for Future Use in Oral Treatment of Fungal Infections
title_full Tablet of Ximenia Americana L. Developed from Mucoadhesive Polymers for Future Use in Oral Treatment of Fungal Infections
title_fullStr Tablet of Ximenia Americana L. Developed from Mucoadhesive Polymers for Future Use in Oral Treatment of Fungal Infections
title_full_unstemmed Tablet of Ximenia Americana L. Developed from Mucoadhesive Polymers for Future Use in Oral Treatment of Fungal Infections
title_short Tablet of Ximenia Americana L. Developed from Mucoadhesive Polymers for Future Use in Oral Treatment of Fungal Infections
title_sort tablet of ximenia americana l. developed from mucoadhesive polymers for future use in oral treatment of fungal infections
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6419192/
https://www.ncbi.nlm.nih.gov/pubmed/30960363
http://dx.doi.org/10.3390/polym11020379
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