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1.
J Microencapsul ; 30(5): 425-31, 2013.
Artículo en Inglés | MEDLINE | ID: mdl-23510368

RESUMEN

Water-in-oil submicron emulsions were used as carrier for the topical delivery of 5-fluorouracil (5FU). The effect of components such as level and hydrophilic-lipophilic balance (HLB) value of surfactant, type of cosurfactant, and drug concentration on the delivery capability of drug in the receptor fluid and in the various skin layers (stratum corneum, epidermis and dermis) were evaluated. The result showed the submicron emulsion could increase the transdermal and deposition of 5FU compared with the aqueous control. Submicron emulsion with surfactant at HLB of 6.0 had higher deposition amount of drug in epidermis layer. The deposition amount of drug in the skin layers increased with increased amounts of surfactant and drug loading of submicron emulsion. However, the 0.2% 5FU-load submicron emulsion showed a comparable deposition effect in various skin layers with the commercial product (5%, Efudix®), which indicated that the submicron emulsions could be a promising drug vehicle for topical application.


Asunto(s)
Antimetabolitos Antineoplásicos/administración & dosificación , Portadores de Fármacos/metabolismo , Emulsiones/metabolismo , Fluorouracilo/administración & dosificación , Absorción Cutánea , Administración Cutánea , Animales , Antimetabolitos Antineoplásicos/farmacocinética , Portadores de Fármacos/química , Emulsiones/química , Fluorouracilo/farmacocinética , Ratas , Ratas Sprague-Dawley , Piel/metabolismo
2.
J Microencapsul ; 28(6): 508-14, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21726123

RESUMEN

Response surface methodology (RSM) was used to develop and optimize the mesomorphic phase formulation for a meloxicam transdermal dosage form. A mixture design was applied to prepare formulations which consisted of three independent variables including oleic acid (X(1)), distilled water (X(2)) and ethanol (X(3)). The flux and lag time (LT) were selected as dependent variables. The result showed that using mesomorphic phases as vehicles can significantly increase flux and shorten LT of drug. The analysis of variance showed that the permeation parameters of meloxicam from formulations were significantly influenced by the independent variables and their interactions. The X(3) (ethanol) had the greatest potential influence on the flux and LT, followed by X(1) and X(2). A new formulation was prepared according to the independent levels provided by RSM. The observed responses were in close agreement with the predicted values, demonstrating that RSM could be successfully used to optimize mesomorphic phase formulations.


Asunto(s)
Antiinflamatorios no Esteroideos/administración & dosificación , Portadores de Fármacos/química , Piel/metabolismo , Tiazinas/administración & dosificación , Tiazoles/administración & dosificación , Administración Cutánea , Animales , Antiinflamatorios no Esteroideos/farmacocinética , Etanol/química , Masculino , Meloxicam , Ácido Oléico/química , Transición de Fase , Ratas , Ratas Sprague-Dawley , Tensoactivos/química , Tiazinas/farmacocinética , Tiazoles/farmacocinética
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