Efeitos da administração tópica da formulação de nanoesfera do malato de sunitinibe na inibição de neovascularização corneana induzida em coelhos

The aim of this study was to compare the sunitinib loaded nanospheres with its free form, in the inhibition of induced corneal neovascularization, in albino rabbits, identifying the degree of inhibition of this neovascularization by measuring the area of corneal neovascularization. The eyes of eleve...

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Detalles Bibliográficos
Autor: Linhares, Luciana Lavigne
Tipo de recurso: tesis de maestría
Estado:Versión publicada
Fecha de publicación:2016
País:Brasil
Institución:Universidade Federal de Goiás (UFG)
Repositorio:Repositório Institucional da UFG
Idioma:portugués
OAI Identifier:oai:repositorio.bc.ufg.br:tede/5840
Acceso en línea:http://repositorio.bc.ufg.br/tede/handle/tede/5840
Access Level:acceso abierto
Palabra clave:Sunitinibe
Neovascularização corneana
Nanoesfera
Nanotecnologia
Angiogênese
Sunitinib
Corneal neovascularization
Nanosphere
Nanotechnology
Angiogenesis
CIENCIAS DA SAUDE::MEDICINA
Descripción
Sumario:The aim of this study was to compare the sunitinib loaded nanospheres with its free form, in the inhibition of induced corneal neovascularization, in albino rabbits, identifying the degree of inhibition of this neovascularization by measuring the area of corneal neovascularization. The eyes of eleven animals were divided into two groups. Group A (right eye of each rabbit) - sunitinib loaded nanospheres and Group B (left eye of each rabbit) - sunitinib solution. Both groups were submited to corneal alkaline burn by sodium hydroxide 1 mol/L. 12 hours after the corneal burn procedure, the group A received topical nanospheres loaded with sunitinib 0.5 mg/mL (Axon Medchem BV, Groningen, Holland), and the group B received 0.5 mg/mL of the sunitinib solution (Axon Medchem BV, Groningen, Holland). Treatment was initiated 12 hours after the surgical and was administered topically 2 times a day during 14 days. After 14 days of treatment all the rabbits were submitted to the examination of the anterior segment slit lamp examination and were photographed using the iSight camera of 8 megapixels with pixels of 1.5 μ. After euthanasia, the eyes were enucleated and sent for histopathological analysis. Neovascularization area in the upper cornea was measured in groups A and B. There was no statistically significant difference between the corneal neovascularization area in each group (p = 0.949). No changes were observed in ophthalmological clinical examination compatible with toxicity to the topical use of sunitinib loaded nanospheres and its free form. No histopathologic diferences were observed in both groups. We conclude that both the free form of sunitinib and sunitinib loaded nanospheres show no difference in inhibiting corneal neovascularization.