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Chitosan gel containing polymeric nanocapsules: a new formulation for vaginal drug delivery
The vaginal route of administration is an alternative for several treatments for either local or systemic pharmacological effects. However, the permanence of a drug in this route represents a challenge for formulation development that can be overcome by using nanoencapsulation and chitosan gel. Thus...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085301/ https://www.ncbi.nlm.nih.gov/pubmed/25061292 http://dx.doi.org/10.2147/IJN.S62599 |
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author | Frank, Luiza A Sandri, Giuseppina D’Autilia, Francesca Contri, Renata V Bonferoni, Maria Cristina Caramella, Carla Frank, Alejandro G Pohlmann, Adriana R Guterres, Silvia S |
author_facet | Frank, Luiza A Sandri, Giuseppina D’Autilia, Francesca Contri, Renata V Bonferoni, Maria Cristina Caramella, Carla Frank, Alejandro G Pohlmann, Adriana R Guterres, Silvia S |
author_sort | Frank, Luiza A |
collection | PubMed |
description | The vaginal route of administration is an alternative for several treatments for either local or systemic pharmacological effects. However, the permanence of a drug in this route represents a challenge for formulation development that can be overcome by using nanoencapsulation and chitosan gel. Thus, this work aimed to evaluate the performance of chitosan hydrogels containing cationic and anionic acrylic-based nanocapsules (Eudragit(®) RS 100 and Eudragit(®) S 100, respectively) with Nile red as a model of lipophilic substance in the vaginal route of administration, as measured by increases in the residence time and the penetration of these formulations. Several formulations were prepared with increasing chitosan concentrations, and were analyzed in terms of pH and rheological behavior so that the most suitable formulation could be selected. The enhancement of the adhesion (tensile stress test and washability profile) and penetration (confocal laser scanning microscopy and extraction followed by quantification) properties of the formulations, when applied to porcine vaginal mucosa, were evaluated. The nanocapsule suspensions produced presented adequate properties: size of approximately 200 nm (polydispersity index of ≤v0.2); zeta potential around +10 mV for the cationic formulation and -10 mV for the anionic formulation; and pH values of 6.1±0.1 (Eudragit RS 100), 5.3±0.2 (Eudragit S 100), 6.2±0.1 (Nile red loaded Eudragit RS 100), and 5.1±0.1 (Nile red loaded Eudragit S 100). The chitosan formulation presented suitable viscosity for vaginal application and acidic pH (approximately 4.5). The tensile stress test showed that both formulations containing polymeric nanocapsules presented higher mucoadhesion when compared with the formulation without nanocapsules. In the washability experiment, no significant differences were found between formulations. Confocal microscopy and fluorescence quantification after extraction from the mucosa showed higher penetration of Nile red when it was nanoencapsulated, particularly in cationic nanocapsules. The formulations developed based on chitosan gel vehicle at 2.5% weight/weight containing polymeric nanocapsules, especially the cationic nanocapsules, demonstrated applicability for the vaginal delivery of hydrophobic substances. |
format | Online Article Text |
id | pubmed-4085301 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-40853012014-07-24 Chitosan gel containing polymeric nanocapsules: a new formulation for vaginal drug delivery Frank, Luiza A Sandri, Giuseppina D’Autilia, Francesca Contri, Renata V Bonferoni, Maria Cristina Caramella, Carla Frank, Alejandro G Pohlmann, Adriana R Guterres, Silvia S Int J Nanomedicine Original Research The vaginal route of administration is an alternative for several treatments for either local or systemic pharmacological effects. However, the permanence of a drug in this route represents a challenge for formulation development that can be overcome by using nanoencapsulation and chitosan gel. Thus, this work aimed to evaluate the performance of chitosan hydrogels containing cationic and anionic acrylic-based nanocapsules (Eudragit(®) RS 100 and Eudragit(®) S 100, respectively) with Nile red as a model of lipophilic substance in the vaginal route of administration, as measured by increases in the residence time and the penetration of these formulations. Several formulations were prepared with increasing chitosan concentrations, and were analyzed in terms of pH and rheological behavior so that the most suitable formulation could be selected. The enhancement of the adhesion (tensile stress test and washability profile) and penetration (confocal laser scanning microscopy and extraction followed by quantification) properties of the formulations, when applied to porcine vaginal mucosa, were evaluated. The nanocapsule suspensions produced presented adequate properties: size of approximately 200 nm (polydispersity index of ≤v0.2); zeta potential around +10 mV for the cationic formulation and -10 mV for the anionic formulation; and pH values of 6.1±0.1 (Eudragit RS 100), 5.3±0.2 (Eudragit S 100), 6.2±0.1 (Nile red loaded Eudragit RS 100), and 5.1±0.1 (Nile red loaded Eudragit S 100). The chitosan formulation presented suitable viscosity for vaginal application and acidic pH (approximately 4.5). The tensile stress test showed that both formulations containing polymeric nanocapsules presented higher mucoadhesion when compared with the formulation without nanocapsules. In the washability experiment, no significant differences were found between formulations. Confocal microscopy and fluorescence quantification after extraction from the mucosa showed higher penetration of Nile red when it was nanoencapsulated, particularly in cationic nanocapsules. The formulations developed based on chitosan gel vehicle at 2.5% weight/weight containing polymeric nanocapsules, especially the cationic nanocapsules, demonstrated applicability for the vaginal delivery of hydrophobic substances. Dove Medical Press 2014-06-28 /pmc/articles/PMC4085301/ /pubmed/25061292 http://dx.doi.org/10.2147/IJN.S62599 Text en © 2014 Frank et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Frank, Luiza A Sandri, Giuseppina D’Autilia, Francesca Contri, Renata V Bonferoni, Maria Cristina Caramella, Carla Frank, Alejandro G Pohlmann, Adriana R Guterres, Silvia S Chitosan gel containing polymeric nanocapsules: a new formulation for vaginal drug delivery |
title | Chitosan gel containing polymeric nanocapsules: a new formulation for vaginal drug delivery |
title_full | Chitosan gel containing polymeric nanocapsules: a new formulation for vaginal drug delivery |
title_fullStr | Chitosan gel containing polymeric nanocapsules: a new formulation for vaginal drug delivery |
title_full_unstemmed | Chitosan gel containing polymeric nanocapsules: a new formulation for vaginal drug delivery |
title_short | Chitosan gel containing polymeric nanocapsules: a new formulation for vaginal drug delivery |
title_sort | chitosan gel containing polymeric nanocapsules: a new formulation for vaginal drug delivery |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4085301/ https://www.ncbi.nlm.nih.gov/pubmed/25061292 http://dx.doi.org/10.2147/IJN.S62599 |
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