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Vaginal Polyelectrolyte Layer-by-Layer Films Based on Chitosan Derivatives and Eudragit(®) S100 for pH Responsive Release of Tenofovir

Women are still at high risk of contracting the human immunodeficiency virus (HIV) virus due to the lack of protection methods under their control, especially in sub-Saharan countries. Polyelectrolyte multilayer smart vaginal films based on chitosan derivatives (chitosan lactate, chitosan tartate, a...

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Autores principales: Cazorla-Luna, Raúl, Martín-Illana, Araceli, Notario-Pérez, Fernando, Bedoya, Luis Miguel, Tamayo, Aitana, Ruiz-Caro, Roberto, Rubio, Juan, Veiga, María-Dolores
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7024361/
https://www.ncbi.nlm.nih.gov/pubmed/31936439
http://dx.doi.org/10.3390/md18010044
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author Cazorla-Luna, Raúl
Martín-Illana, Araceli
Notario-Pérez, Fernando
Bedoya, Luis Miguel
Tamayo, Aitana
Ruiz-Caro, Roberto
Rubio, Juan
Veiga, María-Dolores
author_facet Cazorla-Luna, Raúl
Martín-Illana, Araceli
Notario-Pérez, Fernando
Bedoya, Luis Miguel
Tamayo, Aitana
Ruiz-Caro, Roberto
Rubio, Juan
Veiga, María-Dolores
author_sort Cazorla-Luna, Raúl
collection PubMed
description Women are still at high risk of contracting the human immunodeficiency virus (HIV) virus due to the lack of protection methods under their control, especially in sub-Saharan countries. Polyelectrolyte multilayer smart vaginal films based on chitosan derivatives (chitosan lactate, chitosan tartate, and chitosan citrate) and Eudragit(®) S100 were developed for the pH-sensitive release of Tenofovir. Films were characterized through texture analysis and scanning electron microscopy (SEM). Swelling and drug release studies were carried out in simulated vaginal fluid and a mixture of simulated vaginal and seminal fluids. Ex vivo mucoadhesion was evaluated in bovine vaginal mucosa. SEM micrographs revealed the formation of multilayer films. According to texture analysis, chitosan citrate was the most flexible compared to chitosan tartrate and lactate. The swelling studies showed a moderate water uptake (<300% in all cases), leading to the sustained release of Tenofovir in simulated vaginal fluid (up to 120 h), which was accelerated in the simulated fluid mixture (4–6 h). The films had high mucoadhesion in bovine vaginal mucosa. The multilayer films formed by a mixture of chitosan citrate and Eudragit(®) S100 proved to be the most promising, with zero toxicity, excellent mechanical properties, moderate swelling (<100%), high mucoadhesion capacity, and Tenofovir release of 120 h and 4 h in vaginal fluid and the simulated fluid mixture respectively.
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spelling pubmed-70243612020-03-11 Vaginal Polyelectrolyte Layer-by-Layer Films Based on Chitosan Derivatives and Eudragit(®) S100 for pH Responsive Release of Tenofovir Cazorla-Luna, Raúl Martín-Illana, Araceli Notario-Pérez, Fernando Bedoya, Luis Miguel Tamayo, Aitana Ruiz-Caro, Roberto Rubio, Juan Veiga, María-Dolores Mar Drugs Article Women are still at high risk of contracting the human immunodeficiency virus (HIV) virus due to the lack of protection methods under their control, especially in sub-Saharan countries. Polyelectrolyte multilayer smart vaginal films based on chitosan derivatives (chitosan lactate, chitosan tartate, and chitosan citrate) and Eudragit(®) S100 were developed for the pH-sensitive release of Tenofovir. Films were characterized through texture analysis and scanning electron microscopy (SEM). Swelling and drug release studies were carried out in simulated vaginal fluid and a mixture of simulated vaginal and seminal fluids. Ex vivo mucoadhesion was evaluated in bovine vaginal mucosa. SEM micrographs revealed the formation of multilayer films. According to texture analysis, chitosan citrate was the most flexible compared to chitosan tartrate and lactate. The swelling studies showed a moderate water uptake (<300% in all cases), leading to the sustained release of Tenofovir in simulated vaginal fluid (up to 120 h), which was accelerated in the simulated fluid mixture (4–6 h). The films had high mucoadhesion in bovine vaginal mucosa. The multilayer films formed by a mixture of chitosan citrate and Eudragit(®) S100 proved to be the most promising, with zero toxicity, excellent mechanical properties, moderate swelling (<100%), high mucoadhesion capacity, and Tenofovir release of 120 h and 4 h in vaginal fluid and the simulated fluid mixture respectively. MDPI 2020-01-09 /pmc/articles/PMC7024361/ /pubmed/31936439 http://dx.doi.org/10.3390/md18010044 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
Cazorla-Luna, Raúl
Martín-Illana, Araceli
Notario-Pérez, Fernando
Bedoya, Luis Miguel
Tamayo, Aitana
Ruiz-Caro, Roberto
Rubio, Juan
Veiga, María-Dolores
Vaginal Polyelectrolyte Layer-by-Layer Films Based on Chitosan Derivatives and Eudragit(®) S100 for pH Responsive Release of Tenofovir
title Vaginal Polyelectrolyte Layer-by-Layer Films Based on Chitosan Derivatives and Eudragit(®) S100 for pH Responsive Release of Tenofovir
title_full Vaginal Polyelectrolyte Layer-by-Layer Films Based on Chitosan Derivatives and Eudragit(®) S100 for pH Responsive Release of Tenofovir
title_fullStr Vaginal Polyelectrolyte Layer-by-Layer Films Based on Chitosan Derivatives and Eudragit(®) S100 for pH Responsive Release of Tenofovir
title_full_unstemmed Vaginal Polyelectrolyte Layer-by-Layer Films Based on Chitosan Derivatives and Eudragit(®) S100 for pH Responsive Release of Tenofovir
title_short Vaginal Polyelectrolyte Layer-by-Layer Films Based on Chitosan Derivatives and Eudragit(®) S100 for pH Responsive Release of Tenofovir
title_sort vaginal polyelectrolyte layer-by-layer films based on chitosan derivatives and eudragit(®) s100 for ph responsive release of tenofovir
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7024361/
https://www.ncbi.nlm.nih.gov/pubmed/31936439
http://dx.doi.org/10.3390/md18010044
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