PLGA-corosolic acid implants for potential application in ocular neovascularization diseases

Detalhes bibliográficos
Autor(a) principal: Toledo, Cibele Rodrigues
Data de Publicação: 2020
Outros Autores: Pereira, Vinícius Viana, Andrade, Gracielle Ferreira, Silva-Cunha, Armando
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Brazilian Journal of Pharmaceutical Sciences
Texto Completo: https://www.revistas.usp.br/bjps/article/view/181832
Resumo: Angiogenesis is the formation of new blood vessels from preexisting vasculature. Uncontrolled angiogenesis is associated with progression of several ocular pathologies, such as diabetic retinopathy and macular degeneration. Thus, the inhibition of this process consists in an interesting therapeutic target. Corosolic acid (CA) is a natural derivative of ursolic acid, found in many medicinal herbs and exhibits numerous biological properties, including the antiangiogenic activity. The present study reports the production of CA-loaded poly d,l-lactidecoglycolide acid (PLGA) devices by melt technique. HPLC-UV method was developed and validated to evaluate the uniformity and the release profile of the developed systems. The devices were also characterized by Fourier transform infrared spectroscopy, thermal analysis, and scanning electron morphology. It was studied the antiangiogenic activity of the CA-polymer system, using an in vivo model, the chorioallantoic membrane assay (CAM). CA was dispersed uniformly in the polymer matrix and no chemical interaction between the components of the formulation was verified. The implants presented a sustained release of the drug, which was confirmed by the morphological study and demonstrated an antiangiogenic activity. Therefore, the developed delivery system is a promising therapeutic tool for the treatment of ocular diseases associated with neovascularization or others related to the angiogenic process.
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spelling PLGA-corosolic acid implants for potential application in ocular neovascularization diseasesCorosolic acidPLGAAntiangiogenic activityImplantAngiogenesis is the formation of new blood vessels from preexisting vasculature. Uncontrolled angiogenesis is associated with progression of several ocular pathologies, such as diabetic retinopathy and macular degeneration. Thus, the inhibition of this process consists in an interesting therapeutic target. Corosolic acid (CA) is a natural derivative of ursolic acid, found in many medicinal herbs and exhibits numerous biological properties, including the antiangiogenic activity. The present study reports the production of CA-loaded poly d,l-lactidecoglycolide acid (PLGA) devices by melt technique. HPLC-UV method was developed and validated to evaluate the uniformity and the release profile of the developed systems. The devices were also characterized by Fourier transform infrared spectroscopy, thermal analysis, and scanning electron morphology. It was studied the antiangiogenic activity of the CA-polymer system, using an in vivo model, the chorioallantoic membrane assay (CAM). CA was dispersed uniformly in the polymer matrix and no chemical interaction between the components of the formulation was verified. The implants presented a sustained release of the drug, which was confirmed by the morphological study and demonstrated an antiangiogenic activity. Therefore, the developed delivery system is a promising therapeutic tool for the treatment of ocular diseases associated with neovascularization or others related to the angiogenic process.Universidade de São Paulo. Faculdade de Ciências Farmacêuticas2020-12-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfhttps://www.revistas.usp.br/bjps/article/view/18183210.1590/s2175-97902019000418484Brazilian Journal of Pharmaceutical Sciences; Vol. 56 (2020); e18484Brazilian Journal of Pharmaceutical Sciences; v. 56 (2020); e18484Brazilian Journal of Pharmaceutical Sciences; Vol. 56 (2020); e184842175-97901984-8250reponame:Brazilian Journal of Pharmaceutical Sciencesinstname:Universidade de São Paulo (USP)instacron:USPenghttps://www.revistas.usp.br/bjps/article/view/181832/168734Copyright (c) 2020 Brazilian Journal of Pharmaceutical Scienceshttp://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessToledo, Cibele Rodrigues Pereira, Vinícius Viana Andrade, Gracielle Ferreira Silva-Cunha, Armando 2021-06-12T19:46:54Zoai:revistas.usp.br:article/181832Revistahttps://www.revistas.usp.br/bjps/indexPUBhttps://old.scielo.br/oai/scielo-oai.phpbjps@usp.br||elizabeth.igne@gmail.com2175-97901984-8250opendoar:2021-06-12T19:46:54Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv PLGA-corosolic acid implants for potential application in ocular neovascularization diseases
title PLGA-corosolic acid implants for potential application in ocular neovascularization diseases
spellingShingle PLGA-corosolic acid implants for potential application in ocular neovascularization diseases
Toledo, Cibele Rodrigues
Corosolic acid
PLGA
Antiangiogenic activity
Implant
title_short PLGA-corosolic acid implants for potential application in ocular neovascularization diseases
title_full PLGA-corosolic acid implants for potential application in ocular neovascularization diseases
title_fullStr PLGA-corosolic acid implants for potential application in ocular neovascularization diseases
title_full_unstemmed PLGA-corosolic acid implants for potential application in ocular neovascularization diseases
title_sort PLGA-corosolic acid implants for potential application in ocular neovascularization diseases
author Toledo, Cibele Rodrigues
author_facet Toledo, Cibele Rodrigues
Pereira, Vinícius Viana
Andrade, Gracielle Ferreira
Silva-Cunha, Armando
author_role author
author2 Pereira, Vinícius Viana
Andrade, Gracielle Ferreira
Silva-Cunha, Armando
author2_role author
author
author
dc.contributor.author.fl_str_mv Toledo, Cibele Rodrigues
Pereira, Vinícius Viana
Andrade, Gracielle Ferreira
Silva-Cunha, Armando
dc.subject.por.fl_str_mv Corosolic acid
PLGA
Antiangiogenic activity
Implant
topic Corosolic acid
PLGA
Antiangiogenic activity
Implant
description Angiogenesis is the formation of new blood vessels from preexisting vasculature. Uncontrolled angiogenesis is associated with progression of several ocular pathologies, such as diabetic retinopathy and macular degeneration. Thus, the inhibition of this process consists in an interesting therapeutic target. Corosolic acid (CA) is a natural derivative of ursolic acid, found in many medicinal herbs and exhibits numerous biological properties, including the antiangiogenic activity. The present study reports the production of CA-loaded poly d,l-lactidecoglycolide acid (PLGA) devices by melt technique. HPLC-UV method was developed and validated to evaluate the uniformity and the release profile of the developed systems. The devices were also characterized by Fourier transform infrared spectroscopy, thermal analysis, and scanning electron morphology. It was studied the antiangiogenic activity of the CA-polymer system, using an in vivo model, the chorioallantoic membrane assay (CAM). CA was dispersed uniformly in the polymer matrix and no chemical interaction between the components of the formulation was verified. The implants presented a sustained release of the drug, which was confirmed by the morphological study and demonstrated an antiangiogenic activity. Therefore, the developed delivery system is a promising therapeutic tool for the treatment of ocular diseases associated with neovascularization or others related to the angiogenic process.
publishDate 2020
dc.date.none.fl_str_mv 2020-12-09
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://www.revistas.usp.br/bjps/article/view/181832
10.1590/s2175-97902019000418484
url https://www.revistas.usp.br/bjps/article/view/181832
identifier_str_mv 10.1590/s2175-97902019000418484
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv https://www.revistas.usp.br/bjps/article/view/181832/168734
dc.rights.driver.fl_str_mv Copyright (c) 2020 Brazilian Journal of Pharmaceutical Sciences
http://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv Copyright (c) 2020 Brazilian Journal of Pharmaceutical Sciences
http://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
publisher.none.fl_str_mv Universidade de São Paulo. Faculdade de Ciências Farmacêuticas
dc.source.none.fl_str_mv Brazilian Journal of Pharmaceutical Sciences; Vol. 56 (2020); e18484
Brazilian Journal of Pharmaceutical Sciences; v. 56 (2020); e18484
Brazilian Journal of Pharmaceutical Sciences; Vol. 56 (2020); e18484
2175-9790
1984-8250
reponame:Brazilian Journal of Pharmaceutical Sciences
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Brazilian Journal of Pharmaceutical Sciences
collection Brazilian Journal of Pharmaceutical Sciences
repository.name.fl_str_mv Brazilian Journal of Pharmaceutical Sciences - Universidade de São Paulo (USP)
repository.mail.fl_str_mv bjps@usp.br||elizabeth.igne@gmail.com
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