Ex Vivo Permeation of Carprofen Vehiculated by PLGA Nanoparticles through Porcine Mucous Membranes and Ophthalmic Tissues
(1) Background: Carprofen (CP), 2-(6-chlorocarbazole) propionic acid, is used as an anti-inflammatory, analgesic and anti-pyretic agent and it belongs to the family of non-steroidal anti-inflammatory drugs (NSAIDs). CP has some adverse reactions in systemic administration; for this reason, topical a...
| Autores: | , , , , , |
|---|---|
| Tipo de recurso: | artículo |
| Estado: | Versión publicada |
| Fecha de publicación: | 2020 |
| País: | España |
| Institución: | Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
| Repositorio: | Recercat. Dipósit de la Recerca de Catalunya |
| OAI Identifier: | oai:recercat.cat:2445/161798 |
| Acceso en línea: | https://hdl.handle.net/2445/161798 |
| Access Level: | acceso abierto |
| Palabra clave: | Nanopartícules Solucions (Farmàcia) Sistemes d'alliberament de medicaments Agents antiinflamatoris Malalties dels animals Porc Assaigs clínics Nanoparticles Solutions (Pharmacy) Drug delivery systems Antiinflammatory agents Animal diseases Swine Clinical trials |
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Ex Vivo Permeation of Carprofen Vehiculated by PLGA Nanoparticles through Porcine Mucous Membranes and Ophthalmic TissuesGómez, LidiaParra Coca, AlexanderCalpena Campmany, Ana CristinaGimeno Sandig, ÁlvaroGómez de Aranda Pulgarín, InmaculadaBoix Montañés, Antonio de PáduaNanopartículesSolucions (Farmàcia)Sistemes d'alliberament de medicamentsAgents antiinflamatorisMalalties dels animalsPorcAssaigs clínicsNanoparticlesSolutions (Pharmacy)Drug delivery systemsAntiinflammatory agentsAnimal diseasesSwineClinical trials(1) Background: Carprofen (CP), 2-(6-chlorocarbazole) propionic acid, is used as an anti-inflammatory, analgesic and anti-pyretic agent and it belongs to the family of non-steroidal anti-inflammatory drugs (NSAIDs). CP has some adverse reactions in systemic administration; for this reason, topical administration with CP nanoparticles (CP-NPs) can be an optimal alternative. The main objective of this work is the investigation of ex vivo permeation of CP through different types of porcine mucous membranes (buccal, sublingual and vaginal) and ophthalmic tissues (cornea, sclera and conjunctiva) to compare the influence of CP-NPs formulation over a CP solution (CP-Solution). (2) Methods: The ex vivo permeation profiles were evaluated using Franz diffusion cells. Furthermore, in vivo studies were performed to verify that the formulations did not affect the cell structure and to establish the amount retained (Qr) in the tissues. (3) Results: Permeation of CP-NPs is more effective in terms of drug retention in almost all tissues (with the exception of sclera and sublingual). In vivo studies show that neither of the two formulations affects tissue structure, so both formulations are safe. (4) Conclusions: It was concluded that CP-NPs may be a useful tool for the topical treatment of local inflammation in veterinary and human medicine.MDPI2020202020202020info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://hdl.handle.net/2445/161798Articles publicats en revistes (Farmàcia, Tecnologia Farmacèutica i Fisicoquímica)reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)InglésReproducció del document publicat a: https://doi.org/10.3390/nano10020355Nanomaterials, 2020, vol. 10, num. 2, p. 355https://doi.org/10.3390/nano10020355cc-by (c) Gomez, Lidia et al., 2020http://creativecommons.org/licenses/by/3.0/esinfo:eu-repo/semantics/openAccessoai:recercat.cat:2445/1617982026-05-29T05:05:01Z |
| dc.title.none.fl_str_mv |
Ex Vivo Permeation of Carprofen Vehiculated by PLGA Nanoparticles through Porcine Mucous Membranes and Ophthalmic Tissues |
| title |
Ex Vivo Permeation of Carprofen Vehiculated by PLGA Nanoparticles through Porcine Mucous Membranes and Ophthalmic Tissues |
| spellingShingle |
Ex Vivo Permeation of Carprofen Vehiculated by PLGA Nanoparticles through Porcine Mucous Membranes and Ophthalmic Tissues Gómez, Lidia Nanopartícules Solucions (Farmàcia) Sistemes d'alliberament de medicaments Agents antiinflamatoris Malalties dels animals Porc Assaigs clínics Nanoparticles Solutions (Pharmacy) Drug delivery systems Antiinflammatory agents Animal diseases Swine Clinical trials |
| title_short |
Ex Vivo Permeation of Carprofen Vehiculated by PLGA Nanoparticles through Porcine Mucous Membranes and Ophthalmic Tissues |
| title_full |
Ex Vivo Permeation of Carprofen Vehiculated by PLGA Nanoparticles through Porcine Mucous Membranes and Ophthalmic Tissues |
| title_fullStr |
Ex Vivo Permeation of Carprofen Vehiculated by PLGA Nanoparticles through Porcine Mucous Membranes and Ophthalmic Tissues |
| title_full_unstemmed |
Ex Vivo Permeation of Carprofen Vehiculated by PLGA Nanoparticles through Porcine Mucous Membranes and Ophthalmic Tissues |
| title_sort |
Ex Vivo Permeation of Carprofen Vehiculated by PLGA Nanoparticles through Porcine Mucous Membranes and Ophthalmic Tissues |
| dc.creator.none.fl_str_mv |
Gómez, Lidia Parra Coca, Alexander Calpena Campmany, Ana Cristina Gimeno Sandig, Álvaro Gómez de Aranda Pulgarín, Inmaculada Boix Montañés, Antonio de Pádua |
| author |
Gómez, Lidia |
| author_facet |
Gómez, Lidia Parra Coca, Alexander Calpena Campmany, Ana Cristina Gimeno Sandig, Álvaro Gómez de Aranda Pulgarín, Inmaculada Boix Montañés, Antonio de Pádua |
| author_role |
author |
| author2 |
Parra Coca, Alexander Calpena Campmany, Ana Cristina Gimeno Sandig, Álvaro Gómez de Aranda Pulgarín, Inmaculada Boix Montañés, Antonio de Pádua |
| author2_role |
author author author author author |
| dc.subject.none.fl_str_mv |
Nanopartícules Solucions (Farmàcia) Sistemes d'alliberament de medicaments Agents antiinflamatoris Malalties dels animals Porc Assaigs clínics Nanoparticles Solutions (Pharmacy) Drug delivery systems Antiinflammatory agents Animal diseases Swine Clinical trials |
| topic |
Nanopartícules Solucions (Farmàcia) Sistemes d'alliberament de medicaments Agents antiinflamatoris Malalties dels animals Porc Assaigs clínics Nanoparticles Solutions (Pharmacy) Drug delivery systems Antiinflammatory agents Animal diseases Swine Clinical trials |
| description |
(1) Background: Carprofen (CP), 2-(6-chlorocarbazole) propionic acid, is used as an anti-inflammatory, analgesic and anti-pyretic agent and it belongs to the family of non-steroidal anti-inflammatory drugs (NSAIDs). CP has some adverse reactions in systemic administration; for this reason, topical administration with CP nanoparticles (CP-NPs) can be an optimal alternative. The main objective of this work is the investigation of ex vivo permeation of CP through different types of porcine mucous membranes (buccal, sublingual and vaginal) and ophthalmic tissues (cornea, sclera and conjunctiva) to compare the influence of CP-NPs formulation over a CP solution (CP-Solution). (2) Methods: The ex vivo permeation profiles were evaluated using Franz diffusion cells. Furthermore, in vivo studies were performed to verify that the formulations did not affect the cell structure and to establish the amount retained (Qr) in the tissues. (3) Results: Permeation of CP-NPs is more effective in terms of drug retention in almost all tissues (with the exception of sclera and sublingual). In vivo studies show that neither of the two formulations affects tissue structure, so both formulations are safe. (4) Conclusions: It was concluded that CP-NPs may be a useful tool for the topical treatment of local inflammation in veterinary and human medicine. |
| publishDate |
2020 |
| dc.date.none.fl_str_mv |
2020 2020 2020 2020 |
| dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
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article |
| status_str |
publishedVersion |
| dc.identifier.none.fl_str_mv |
https://hdl.handle.net/2445/161798 |
| url |
https://hdl.handle.net/2445/161798 |
| dc.language.none.fl_str_mv |
Inglés |
| language_invalid_str_mv |
Inglés |
| dc.relation.none.fl_str_mv |
Reproducció del document publicat a: https://doi.org/10.3390/nano10020355 Nanomaterials, 2020, vol. 10, num. 2, p. 355 https://doi.org/10.3390/nano10020355 |
| dc.rights.none.fl_str_mv |
cc-by (c) Gomez, Lidia et al., 2020 http://creativecommons.org/licenses/by/3.0/es info:eu-repo/semantics/openAccess |
| rights_invalid_str_mv |
cc-by (c) Gomez, Lidia et al., 2020 http://creativecommons.org/licenses/by/3.0/es |
| eu_rights_str_mv |
openAccess |
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application/pdf |
| dc.publisher.none.fl_str_mv |
MDPI |
| publisher.none.fl_str_mv |
MDPI |
| dc.source.none.fl_str_mv |
Articles publicats en revistes (Farmàcia, Tecnologia Farmacèutica i Fisicoquímica) reponame:Recercat. Dipósit de la Recerca de Catalunya instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya) |
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Recercat. Dipósit de la Recerca de Catalunya |
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Recercat. Dipósit de la Recerca de Catalunya |
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