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Int J Nanomedicine ; 10: 5529-42, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26366075

RESUMO

Nanoemulsions are drug delivery systems that may increase the penetration of lipophilic compounds through the skin, enhancing their topical effect. Chalcones are compounds of low water solubility that have been described as promising molecules for the treatment of cutaneous leishmaniasis (CL). In this context, the aim of this work was to optimize the development of a nanoemulsion containing a synthetic chalcone for CL treatment using a 2(2) full factorial design. The formulations were prepared by spontaneous emulsification and the experimental design studied the influence of two independent variables (type of surfactant - soybean lecithin or sorbitan monooleate and type of co-surfactants - polysorbate 20 or polysorbate 80) on the physicochemical characteristics of the nanoemulsions, as well as on the skin permeation/retention of the synthetic chalcone in porcine skin. In order to evaluate the stability of the systems, the antileishmanial assay was performed against Leishmania amazonensis 24 hours and 60 days after the preparation of the nanoemulsions. The formulation composed of soybean lecithin and polysorbate 20 presented suitable physicochemical characteristics (droplet size 171.9 nm; polydispersity index 0.14; zeta potential -39.43 mV; pH 5.16; and viscosity 2.00 cP), drug content (91.09%) and the highest retention in dermis (3.03 µg·g(-1)) - the main response of interest - confirmed by confocal microscopy. This formulation also presented better stability of leishmanicidal activity in vitro against L. amazonensis amastigote forms (half maximal inhibitory concentration value 0.32±0.05 µM), which confirmed the potential of the nanoemulsion soybean lecithin and polysorbate 20 for CL treatment.


Assuntos
Antiparasitários/farmacologia , Chalcona/farmacologia , Sistemas de Liberação de Medicamentos , Leishmaniose Cutânea/tratamento farmacológico , Nanoestruturas/química , Administração Cutânea , Antiparasitários/química , Linhagem Celular Tumoral , Chalcona/química , Fenômenos Químicos , Emulsões , Humanos , Concentração de Íons de Hidrogênio , Concentração Inibidora 50 , Lecitinas/química , Lecitinas/farmacologia , Tamanho da Partícula , Polissorbatos/química , Polissorbatos/farmacologia , Pele/efeitos dos fármacos , Pele/parasitologia , Solubilidade , Relação Estrutura-Atividade , Tensoativos/química , Tensoativos/farmacologia , Viscosidade
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