Single and mixed poloxamine micelles as nanocarriers for solubilization and sustained release of ethoxzolamide for topical glaucoma therapy
- Autores
- Ribeiro, Andreza; Sosnik, Alejandro Dario; Chiappetta, Diego Andrés; Veiga, Francisco; Concheiro, Angel; Alvarez Lorenzo, Carmen
- Año de publicación
- 2012
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Polymeric micelles of single and mixed poloxamines (Tetronic) were evaluated regarding their ability to host the antiglaucoma agent ethoxzolamide (ETOX) for topical ocular application. Three highly hydrophilic varieties of poloxamine (T908, T1107 and T1307) and a medium hydrophilic variety (T904), possessing a similar number of propylene oxide units but different contents in ethylene oxide, were chosen for the study. The critical micellar concentration and the cloud point of mixed micelles in 0.9 per cent NaCl were slightly greater than the values predicted from the additive rule, suggesting that the co-micellization is hindered. Micellar size ranged between 17 and 120 nm and it was not altered after the loading of ETOX (2.7-11.5 mg drug g-1 poloxamine). Drug solubilization ability ranked in the order: T904 (50-fold increase in the apparent solubility) > T1107 ≅ T1307 > T908. Mixed micelles showed an intermediate capability to host ETOX but a greater physical stability, maintaining almost 100 per cent drug solubilized after 28 days. Furthermore, the different structural features of poloxamines and their combination in mixed micelles enabled the tuning of drug release profiles, sustaining the release in the 1-5 days range. These findings together with promising hen's egg test-chorioallantoic membrane biocompatibility tests make poloxamine micelles promising nanocarriers for carbonic anhydrase inhibitors in the treatment of glaucoma.
Fil: Ribeiro, Andreza. Universidad de Santiago de Compostela; España
Fil: Sosnik, Alejandro Dario. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Tecnología Farmacéutica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Chiappetta, Diego Andrés. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Tecnología Farmacéutica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Veiga, Francisco. Universidad de Coimbra; Portugal
Fil: Concheiro, Angel. Universidad de Santiago de Compostela; España
Fil: Alvarez Lorenzo, Carmen. Universidad de Santiago de Compostela; España - Materia
-
CARBONIC ANHYDRASE INHIBITOR SOLUBILIZATION
ETHOXZOLAMIDE
OCULAR DELIVERY
POLOXAMINE
POLY(ETHYLENE OXIDE)-POLY(PROPYLENE OXIDE) BLOCK COPOLYMER
POLYMERIC MICELLES - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/197313
Ver los metadatos del registro completo
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oai:ri.conicet.gov.ar:11336/197313 |
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repository_id_str |
3498 |
network_name_str |
CONICET Digital (CONICET) |
spelling |
Single and mixed poloxamine micelles as nanocarriers for solubilization and sustained release of ethoxzolamide for topical glaucoma therapyRibeiro, AndrezaSosnik, Alejandro DarioChiappetta, Diego AndrésVeiga, FranciscoConcheiro, AngelAlvarez Lorenzo, CarmenCARBONIC ANHYDRASE INHIBITOR SOLUBILIZATIONETHOXZOLAMIDEOCULAR DELIVERYPOLOXAMINEPOLY(ETHYLENE OXIDE)-POLY(PROPYLENE OXIDE) BLOCK COPOLYMERPOLYMERIC MICELLEShttps://purl.org/becyt/ford/2.10https://purl.org/becyt/ford/2Polymeric micelles of single and mixed poloxamines (Tetronic) were evaluated regarding their ability to host the antiglaucoma agent ethoxzolamide (ETOX) for topical ocular application. Three highly hydrophilic varieties of poloxamine (T908, T1107 and T1307) and a medium hydrophilic variety (T904), possessing a similar number of propylene oxide units but different contents in ethylene oxide, were chosen for the study. The critical micellar concentration and the cloud point of mixed micelles in 0.9 per cent NaCl were slightly greater than the values predicted from the additive rule, suggesting that the co-micellization is hindered. Micellar size ranged between 17 and 120 nm and it was not altered after the loading of ETOX (2.7-11.5 mg drug g-1 poloxamine). Drug solubilization ability ranked in the order: T904 (50-fold increase in the apparent solubility) > T1107 ≅ T1307 > T908. Mixed micelles showed an intermediate capability to host ETOX but a greater physical stability, maintaining almost 100 per cent drug solubilized after 28 days. Furthermore, the different structural features of poloxamines and their combination in mixed micelles enabled the tuning of drug release profiles, sustaining the release in the 1-5 days range. These findings together with promising hen's egg test-chorioallantoic membrane biocompatibility tests make poloxamine micelles promising nanocarriers for carbonic anhydrase inhibitors in the treatment of glaucoma.Fil: Ribeiro, Andreza. Universidad de Santiago de Compostela; EspañaFil: Sosnik, Alejandro Dario. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Tecnología Farmacéutica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Chiappetta, Diego Andrés. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Tecnología Farmacéutica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Veiga, Francisco. Universidad de Coimbra; PortugalFil: Concheiro, Angel. Universidad de Santiago de Compostela; EspañaFil: Alvarez Lorenzo, Carmen. Universidad de Santiago de Compostela; EspañaThe Royal Society2012-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/197313Ribeiro, Andreza; Sosnik, Alejandro Dario; Chiappetta, Diego Andrés; Veiga, Francisco; Concheiro, Angel; et al.; Single and mixed poloxamine micelles as nanocarriers for solubilization and sustained release of ethoxzolamide for topical glaucoma therapy; The Royal Society; Journal of the Royal Society Interface; 9; 74; 9-2012; 2059-20691742-5689CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://rsif.royalsocietypublishing.org/content/9/74/2059.full.pdf+htmlinfo:eu-repo/semantics/altIdentifier/doi/10.1098/rsif.2012.0102info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:09:03Zoai:ri.conicet.gov.ar:11336/197313instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-10 13:09:04.268CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Single and mixed poloxamine micelles as nanocarriers for solubilization and sustained release of ethoxzolamide for topical glaucoma therapy |
title |
Single and mixed poloxamine micelles as nanocarriers for solubilization and sustained release of ethoxzolamide for topical glaucoma therapy |
spellingShingle |
Single and mixed poloxamine micelles as nanocarriers for solubilization and sustained release of ethoxzolamide for topical glaucoma therapy Ribeiro, Andreza CARBONIC ANHYDRASE INHIBITOR SOLUBILIZATION ETHOXZOLAMIDE OCULAR DELIVERY POLOXAMINE POLY(ETHYLENE OXIDE)-POLY(PROPYLENE OXIDE) BLOCK COPOLYMER POLYMERIC MICELLES |
title_short |
Single and mixed poloxamine micelles as nanocarriers for solubilization and sustained release of ethoxzolamide for topical glaucoma therapy |
title_full |
Single and mixed poloxamine micelles as nanocarriers for solubilization and sustained release of ethoxzolamide for topical glaucoma therapy |
title_fullStr |
Single and mixed poloxamine micelles as nanocarriers for solubilization and sustained release of ethoxzolamide for topical glaucoma therapy |
title_full_unstemmed |
Single and mixed poloxamine micelles as nanocarriers for solubilization and sustained release of ethoxzolamide for topical glaucoma therapy |
title_sort |
Single and mixed poloxamine micelles as nanocarriers for solubilization and sustained release of ethoxzolamide for topical glaucoma therapy |
dc.creator.none.fl_str_mv |
Ribeiro, Andreza Sosnik, Alejandro Dario Chiappetta, Diego Andrés Veiga, Francisco Concheiro, Angel Alvarez Lorenzo, Carmen |
author |
Ribeiro, Andreza |
author_facet |
Ribeiro, Andreza Sosnik, Alejandro Dario Chiappetta, Diego Andrés Veiga, Francisco Concheiro, Angel Alvarez Lorenzo, Carmen |
author_role |
author |
author2 |
Sosnik, Alejandro Dario Chiappetta, Diego Andrés Veiga, Francisco Concheiro, Angel Alvarez Lorenzo, Carmen |
author2_role |
author author author author author |
dc.subject.none.fl_str_mv |
CARBONIC ANHYDRASE INHIBITOR SOLUBILIZATION ETHOXZOLAMIDE OCULAR DELIVERY POLOXAMINE POLY(ETHYLENE OXIDE)-POLY(PROPYLENE OXIDE) BLOCK COPOLYMER POLYMERIC MICELLES |
topic |
CARBONIC ANHYDRASE INHIBITOR SOLUBILIZATION ETHOXZOLAMIDE OCULAR DELIVERY POLOXAMINE POLY(ETHYLENE OXIDE)-POLY(PROPYLENE OXIDE) BLOCK COPOLYMER POLYMERIC MICELLES |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/2.10 https://purl.org/becyt/ford/2 |
dc.description.none.fl_txt_mv |
Polymeric micelles of single and mixed poloxamines (Tetronic) were evaluated regarding their ability to host the antiglaucoma agent ethoxzolamide (ETOX) for topical ocular application. Three highly hydrophilic varieties of poloxamine (T908, T1107 and T1307) and a medium hydrophilic variety (T904), possessing a similar number of propylene oxide units but different contents in ethylene oxide, were chosen for the study. The critical micellar concentration and the cloud point of mixed micelles in 0.9 per cent NaCl were slightly greater than the values predicted from the additive rule, suggesting that the co-micellization is hindered. Micellar size ranged between 17 and 120 nm and it was not altered after the loading of ETOX (2.7-11.5 mg drug g-1 poloxamine). Drug solubilization ability ranked in the order: T904 (50-fold increase in the apparent solubility) > T1107 ≅ T1307 > T908. Mixed micelles showed an intermediate capability to host ETOX but a greater physical stability, maintaining almost 100 per cent drug solubilized after 28 days. Furthermore, the different structural features of poloxamines and their combination in mixed micelles enabled the tuning of drug release profiles, sustaining the release in the 1-5 days range. These findings together with promising hen's egg test-chorioallantoic membrane biocompatibility tests make poloxamine micelles promising nanocarriers for carbonic anhydrase inhibitors in the treatment of glaucoma. Fil: Ribeiro, Andreza. Universidad de Santiago de Compostela; España Fil: Sosnik, Alejandro Dario. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Tecnología Farmacéutica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Chiappetta, Diego Andrés. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Tecnología Farmacéutica; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Veiga, Francisco. Universidad de Coimbra; Portugal Fil: Concheiro, Angel. Universidad de Santiago de Compostela; España Fil: Alvarez Lorenzo, Carmen. Universidad de Santiago de Compostela; España |
description |
Polymeric micelles of single and mixed poloxamines (Tetronic) were evaluated regarding their ability to host the antiglaucoma agent ethoxzolamide (ETOX) for topical ocular application. Three highly hydrophilic varieties of poloxamine (T908, T1107 and T1307) and a medium hydrophilic variety (T904), possessing a similar number of propylene oxide units but different contents in ethylene oxide, were chosen for the study. The critical micellar concentration and the cloud point of mixed micelles in 0.9 per cent NaCl were slightly greater than the values predicted from the additive rule, suggesting that the co-micellization is hindered. Micellar size ranged between 17 and 120 nm and it was not altered after the loading of ETOX (2.7-11.5 mg drug g-1 poloxamine). Drug solubilization ability ranked in the order: T904 (50-fold increase in the apparent solubility) > T1107 ≅ T1307 > T908. Mixed micelles showed an intermediate capability to host ETOX but a greater physical stability, maintaining almost 100 per cent drug solubilized after 28 days. Furthermore, the different structural features of poloxamines and their combination in mixed micelles enabled the tuning of drug release profiles, sustaining the release in the 1-5 days range. These findings together with promising hen's egg test-chorioallantoic membrane biocompatibility tests make poloxamine micelles promising nanocarriers for carbonic anhydrase inhibitors in the treatment of glaucoma. |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-09 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/197313 Ribeiro, Andreza; Sosnik, Alejandro Dario; Chiappetta, Diego Andrés; Veiga, Francisco; Concheiro, Angel; et al.; Single and mixed poloxamine micelles as nanocarriers for solubilization and sustained release of ethoxzolamide for topical glaucoma therapy; The Royal Society; Journal of the Royal Society Interface; 9; 74; 9-2012; 2059-2069 1742-5689 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/197313 |
identifier_str_mv |
Ribeiro, Andreza; Sosnik, Alejandro Dario; Chiappetta, Diego Andrés; Veiga, Francisco; Concheiro, Angel; et al.; Single and mixed poloxamine micelles as nanocarriers for solubilization and sustained release of ethoxzolamide for topical glaucoma therapy; The Royal Society; Journal of the Royal Society Interface; 9; 74; 9-2012; 2059-2069 1742-5689 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://rsif.royalsocietypublishing.org/content/9/74/2059.full.pdf+html info:eu-repo/semantics/altIdentifier/doi/10.1098/rsif.2012.0102 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
The Royal Society |
publisher.none.fl_str_mv |
The Royal Society |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1842980440210669568 |
score |
12.993085 |