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Bimatoprost-Loaded Ocular Inserts as Sustained Release Drug Delivery Systems for Glaucoma Treatment: In Vitro and In Vivo Evaluation

The purpose of the present study was to develop and assess a novel sustained-release drug delivery system of Bimatoprost (BIM). Chitosan polymeric inserts were prepared using the solvent casting method and characterized by swelling studies, infrared spectroscopy, differential scanning calorimetry, d...

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Autores principales: Franca, Juçara Ribeiro, Foureaux, Giselle, Fuscaldi, Leonardo Lima, Ribeiro, Tatiana Gomes, Rodrigues, Lívia Bomfim, Bravo, Renata, Castilho, Rachel Oliveira, Yoshida, Maria Irene, Cardoso, Valbert Nascimento, Fernandes, Simone Odília, Cronemberger, Sebastião, Ferreira, Anderson José, Faraco, André Augusto Gomes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005758/
https://www.ncbi.nlm.nih.gov/pubmed/24788066
http://dx.doi.org/10.1371/journal.pone.0095461
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author Franca, Juçara Ribeiro
Foureaux, Giselle
Fuscaldi, Leonardo Lima
Ribeiro, Tatiana Gomes
Rodrigues, Lívia Bomfim
Bravo, Renata
Castilho, Rachel Oliveira
Yoshida, Maria Irene
Cardoso, Valbert Nascimento
Fernandes, Simone Odília
Cronemberger, Sebastião
Ferreira, Anderson José
Faraco, André Augusto Gomes
author_facet Franca, Juçara Ribeiro
Foureaux, Giselle
Fuscaldi, Leonardo Lima
Ribeiro, Tatiana Gomes
Rodrigues, Lívia Bomfim
Bravo, Renata
Castilho, Rachel Oliveira
Yoshida, Maria Irene
Cardoso, Valbert Nascimento
Fernandes, Simone Odília
Cronemberger, Sebastião
Ferreira, Anderson José
Faraco, André Augusto Gomes
author_sort Franca, Juçara Ribeiro
collection PubMed
description The purpose of the present study was to develop and assess a novel sustained-release drug delivery system of Bimatoprost (BIM). Chitosan polymeric inserts were prepared using the solvent casting method and characterized by swelling studies, infrared spectroscopy, differential scanning calorimetry, drug content, scanning electron microscopy and in vitro drug release. Biodistribution of (99m)Tc-BIM eye drops and (99m)Tc-BIM-loaded inserts, after ocular administration in Wistar rats, was accessed by ex vivo radiation counting. The inserts were evaluated for their therapeutic efficacy in glaucomatous Wistar rats. Glaucoma was induced by weekly intracameral injection of hyaluronic acid. BIM-loaded inserts (equivalent to 9.0 µg BIM) were administered once into conjunctival sac, after ocular hypertension confirmation. BIM eye drop was topically instilled in a second group of glaucomatous rats for 15 days days, while placebo inserts were administered once in a third group. An untreated glaucomatous group was used as control. Intraocular pressure (IOP) was monitored for four consecutive weeks after treatment began. At the end of the experiment, retinal ganglion cells and optic nerve head cupping were evaluated in the histological eye sections. Characterization results revealed that the drug physically interacted, but did not chemically react with the polymeric matrix. Inserts sustainedly released BIM in vitro during 8 hours. Biodistribution studies showed that the amount of (99m)Tc-BIM that remained in the eye was significantly lower after eye drop instillation than after chitosan insert implantation. BIM-loaded inserts lowered IOP for 4 weeks, after one application, while IOP values remained significantly high for the placebo and untreated groups. Eye drops were only effective during the daily treatment period. IOP results were reflected in RGC counting and optic nerve head cupping damage. BIM-loaded inserts provided sustained release of BIM and seem to be a promising system for glaucoma management.
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spelling pubmed-40057582014-05-09 Bimatoprost-Loaded Ocular Inserts as Sustained Release Drug Delivery Systems for Glaucoma Treatment: In Vitro and In Vivo Evaluation Franca, Juçara Ribeiro Foureaux, Giselle Fuscaldi, Leonardo Lima Ribeiro, Tatiana Gomes Rodrigues, Lívia Bomfim Bravo, Renata Castilho, Rachel Oliveira Yoshida, Maria Irene Cardoso, Valbert Nascimento Fernandes, Simone Odília Cronemberger, Sebastião Ferreira, Anderson José Faraco, André Augusto Gomes PLoS One Research Article The purpose of the present study was to develop and assess a novel sustained-release drug delivery system of Bimatoprost (BIM). Chitosan polymeric inserts were prepared using the solvent casting method and characterized by swelling studies, infrared spectroscopy, differential scanning calorimetry, drug content, scanning electron microscopy and in vitro drug release. Biodistribution of (99m)Tc-BIM eye drops and (99m)Tc-BIM-loaded inserts, after ocular administration in Wistar rats, was accessed by ex vivo radiation counting. The inserts were evaluated for their therapeutic efficacy in glaucomatous Wistar rats. Glaucoma was induced by weekly intracameral injection of hyaluronic acid. BIM-loaded inserts (equivalent to 9.0 µg BIM) were administered once into conjunctival sac, after ocular hypertension confirmation. BIM eye drop was topically instilled in a second group of glaucomatous rats for 15 days days, while placebo inserts were administered once in a third group. An untreated glaucomatous group was used as control. Intraocular pressure (IOP) was monitored for four consecutive weeks after treatment began. At the end of the experiment, retinal ganglion cells and optic nerve head cupping were evaluated in the histological eye sections. Characterization results revealed that the drug physically interacted, but did not chemically react with the polymeric matrix. Inserts sustainedly released BIM in vitro during 8 hours. Biodistribution studies showed that the amount of (99m)Tc-BIM that remained in the eye was significantly lower after eye drop instillation than after chitosan insert implantation. BIM-loaded inserts lowered IOP for 4 weeks, after one application, while IOP values remained significantly high for the placebo and untreated groups. Eye drops were only effective during the daily treatment period. IOP results were reflected in RGC counting and optic nerve head cupping damage. BIM-loaded inserts provided sustained release of BIM and seem to be a promising system for glaucoma management. Public Library of Science 2014-04-30 /pmc/articles/PMC4005758/ /pubmed/24788066 http://dx.doi.org/10.1371/journal.pone.0095461 Text en © 2014 Franca et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Franca, Juçara Ribeiro
Foureaux, Giselle
Fuscaldi, Leonardo Lima
Ribeiro, Tatiana Gomes
Rodrigues, Lívia Bomfim
Bravo, Renata
Castilho, Rachel Oliveira
Yoshida, Maria Irene
Cardoso, Valbert Nascimento
Fernandes, Simone Odília
Cronemberger, Sebastião
Ferreira, Anderson José
Faraco, André Augusto Gomes
Bimatoprost-Loaded Ocular Inserts as Sustained Release Drug Delivery Systems for Glaucoma Treatment: In Vitro and In Vivo Evaluation
title Bimatoprost-Loaded Ocular Inserts as Sustained Release Drug Delivery Systems for Glaucoma Treatment: In Vitro and In Vivo Evaluation
title_full Bimatoprost-Loaded Ocular Inserts as Sustained Release Drug Delivery Systems for Glaucoma Treatment: In Vitro and In Vivo Evaluation
title_fullStr Bimatoprost-Loaded Ocular Inserts as Sustained Release Drug Delivery Systems for Glaucoma Treatment: In Vitro and In Vivo Evaluation
title_full_unstemmed Bimatoprost-Loaded Ocular Inserts as Sustained Release Drug Delivery Systems for Glaucoma Treatment: In Vitro and In Vivo Evaluation
title_short Bimatoprost-Loaded Ocular Inserts as Sustained Release Drug Delivery Systems for Glaucoma Treatment: In Vitro and In Vivo Evaluation
title_sort bimatoprost-loaded ocular inserts as sustained release drug delivery systems for glaucoma treatment: in vitro and in vivo evaluation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4005758/
https://www.ncbi.nlm.nih.gov/pubmed/24788066
http://dx.doi.org/10.1371/journal.pone.0095461
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