In situ Formed Implants, Based on PLGA and Eudragit Blends, for Novel Florfenicol Controlled Release Formulations
- Autores
- Karp, Federico; Turino, Ludmila Noelia; Helbling, Ignacio Marcelo; Islan, Germán Abel; Luna, Julio Alberto; Estenoz, Diana Alejandra
- Año de publicación
- 2021
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Drug controlled release technologies (DCRTs) represent an opportunity for designing new therapies. Main objectives are dose number optimization and secondary effects reduction to improve the level of patient/client acceptance. The present work studies DCRTs based in blended polymeric implants for single dose and long-term therapies of florfenicol (FF), a broad spectrum antibiotic. Polymers used were PLGA and Eudragit E100/S100 types. Eudragit/PLGA and FF/PLGA ratios were the main studied factors in terms of encapsulation efficiencies (EEs) and drug release profiles. In addition, morphological and physicochemical characterization were carried out. EEs were of 50-100% depending on formulation composition, and the FF releasing rate was increased or diminished when E100 or S100 were added, respectively. PLGA hydrolytic cleavage products possibly affect Eudragit solubility and matrix stability. Different mathematical models were used for better understanding and simulating release processes. Implants maintained the antimicrobial activity against Pseudomonas aeruginosa up to 12 days on agar plates. The developed DCRTs represents a suitable alternative for florfenicol long-term therapies.
Centro de Investigación y Desarrollo en Fermentaciones Industriales - Materia
-
Química
Farmacia
Drug delivery systems
Polymers
Antibiotics
Florfenicol
Controlled release
Biocompatible solvent
Biocompatible polymers
PLGA
Eudragit polymers
Autocatalytic effect - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-sa/4.0/
- Repositorio
- Institución
- Universidad Nacional de La Plata
- OAI Identificador
- oai:sedici.unlp.edu.ar:10915/132559
Ver los metadatos del registro completo
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In situ Formed Implants, Based on PLGA and Eudragit Blends, for Novel Florfenicol Controlled Release FormulationsKarp, FedericoTurino, Ludmila NoeliaHelbling, Ignacio MarceloIslan, Germán AbelLuna, Julio AlbertoEstenoz, Diana AlejandraQuímicaFarmaciaDrug delivery systemsPolymersAntibioticsFlorfenicolControlled releaseBiocompatible solventBiocompatible polymersPLGAEudragit polymersAutocatalytic effectDrug controlled release technologies (DCRTs) represent an opportunity for designing new therapies. Main objectives are dose number optimization and secondary effects reduction to improve the level of patient/client acceptance. The present work studies DCRTs based in blended polymeric implants for single dose and long-term therapies of florfenicol (FF), a broad spectrum antibiotic. Polymers used were PLGA and Eudragit E100/S100 types. Eudragit/PLGA and FF/PLGA ratios were the main studied factors in terms of encapsulation efficiencies (EEs) and drug release profiles. In addition, morphological and physicochemical characterization were carried out. EEs were of 50-100% depending on formulation composition, and the FF releasing rate was increased or diminished when E100 or S100 were added, respectively. PLGA hydrolytic cleavage products possibly affect Eudragit solubility and matrix stability. Different mathematical models were used for better understanding and simulating release processes. Implants maintained the antimicrobial activity against Pseudomonas aeruginosa up to 12 days on agar plates. The developed DCRTs represents a suitable alternative for florfenicol long-term therapies.Centro de Investigación y Desarrollo en Fermentaciones Industriales2021info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf1270-1278http://sedici.unlp.edu.ar/handle/10915/132559enginfo:eu-repo/semantics/altIdentifier/issn/1520-6017info:eu-repo/semantics/altIdentifier/issn/0022-3549info:eu-repo/semantics/altIdentifier/doi/10.1016/j.xphs.2020.11.006info:eu-repo/semantics/altIdentifier/pmid/33217426info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:32:36Zoai:sedici.unlp.edu.ar:10915/132559Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:32:37.149SEDICI (UNLP) - Universidad Nacional de La Platafalse |
dc.title.none.fl_str_mv |
In situ Formed Implants, Based on PLGA and Eudragit Blends, for Novel Florfenicol Controlled Release Formulations |
title |
In situ Formed Implants, Based on PLGA and Eudragit Blends, for Novel Florfenicol Controlled Release Formulations |
spellingShingle |
In situ Formed Implants, Based on PLGA and Eudragit Blends, for Novel Florfenicol Controlled Release Formulations Karp, Federico Química Farmacia Drug delivery systems Polymers Antibiotics Florfenicol Controlled release Biocompatible solvent Biocompatible polymers PLGA Eudragit polymers Autocatalytic effect |
title_short |
In situ Formed Implants, Based on PLGA and Eudragit Blends, for Novel Florfenicol Controlled Release Formulations |
title_full |
In situ Formed Implants, Based on PLGA and Eudragit Blends, for Novel Florfenicol Controlled Release Formulations |
title_fullStr |
In situ Formed Implants, Based on PLGA and Eudragit Blends, for Novel Florfenicol Controlled Release Formulations |
title_full_unstemmed |
In situ Formed Implants, Based on PLGA and Eudragit Blends, for Novel Florfenicol Controlled Release Formulations |
title_sort |
In situ Formed Implants, Based on PLGA and Eudragit Blends, for Novel Florfenicol Controlled Release Formulations |
dc.creator.none.fl_str_mv |
Karp, Federico Turino, Ludmila Noelia Helbling, Ignacio Marcelo Islan, Germán Abel Luna, Julio Alberto Estenoz, Diana Alejandra |
author |
Karp, Federico |
author_facet |
Karp, Federico Turino, Ludmila Noelia Helbling, Ignacio Marcelo Islan, Germán Abel Luna, Julio Alberto Estenoz, Diana Alejandra |
author_role |
author |
author2 |
Turino, Ludmila Noelia Helbling, Ignacio Marcelo Islan, Germán Abel Luna, Julio Alberto Estenoz, Diana Alejandra |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
Química Farmacia Drug delivery systems Polymers Antibiotics Florfenicol Controlled release Biocompatible solvent Biocompatible polymers PLGA Eudragit polymers Autocatalytic effect |
topic |
Química Farmacia Drug delivery systems Polymers Antibiotics Florfenicol Controlled release Biocompatible solvent Biocompatible polymers PLGA Eudragit polymers Autocatalytic effect |
dc.description.none.fl_txt_mv |
Drug controlled release technologies (DCRTs) represent an opportunity for designing new therapies. Main objectives are dose number optimization and secondary effects reduction to improve the level of patient/client acceptance. The present work studies DCRTs based in blended polymeric implants for single dose and long-term therapies of florfenicol (FF), a broad spectrum antibiotic. Polymers used were PLGA and Eudragit E100/S100 types. Eudragit/PLGA and FF/PLGA ratios were the main studied factors in terms of encapsulation efficiencies (EEs) and drug release profiles. In addition, morphological and physicochemical characterization were carried out. EEs were of 50-100% depending on formulation composition, and the FF releasing rate was increased or diminished when E100 or S100 were added, respectively. PLGA hydrolytic cleavage products possibly affect Eudragit solubility and matrix stability. Different mathematical models were used for better understanding and simulating release processes. Implants maintained the antimicrobial activity against Pseudomonas aeruginosa up to 12 days on agar plates. The developed DCRTs represents a suitable alternative for florfenicol long-term therapies. Centro de Investigación y Desarrollo en Fermentaciones Industriales |
description |
Drug controlled release technologies (DCRTs) represent an opportunity for designing new therapies. Main objectives are dose number optimization and secondary effects reduction to improve the level of patient/client acceptance. The present work studies DCRTs based in blended polymeric implants for single dose and long-term therapies of florfenicol (FF), a broad spectrum antibiotic. Polymers used were PLGA and Eudragit E100/S100 types. Eudragit/PLGA and FF/PLGA ratios were the main studied factors in terms of encapsulation efficiencies (EEs) and drug release profiles. In addition, morphological and physicochemical characterization were carried out. EEs were of 50-100% depending on formulation composition, and the FF releasing rate was increased or diminished when E100 or S100 were added, respectively. PLGA hydrolytic cleavage products possibly affect Eudragit solubility and matrix stability. Different mathematical models were used for better understanding and simulating release processes. Implants maintained the antimicrobial activity against Pseudomonas aeruginosa up to 12 days on agar plates. The developed DCRTs represents a suitable alternative for florfenicol long-term therapies. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Articulo http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
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publishedVersion |
dc.identifier.none.fl_str_mv |
http://sedici.unlp.edu.ar/handle/10915/132559 |
url |
http://sedici.unlp.edu.ar/handle/10915/132559 |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
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