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AAPS PharmSciTech ; 14(4): 1294-302, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23975571

RESUMO

The aim of the study was to investigate the factors affecting the stability and performance of ipratropium bromide and fenoterol hydrobromide in a pressurized-metered dose inhaler (pMDI). A factorial design was applied to investigate the effects of three parameters (propellant, water, and ethanol) on the performance of 27 designed formulations of a solution-based pMDI. The formulations that contained a hydrofluoroalkane (HFA) propellant lower than 72% v/v and an ethanol concentration higher than 27% v/v remained as clear solutions. Nine formulations that contained the HFA propellant higher than 74% v/v precipitated. The results indicated that it was not only the HFA propellant content of the formulations that was related to the formulation instability but also ethanol content. Only six formulations from the 18 formulations, that did not precipitate, produced drug contents that were within the acceptable range (80-120%). These six formulations generated aerosols with mass median aerodynamic diameters (MMAD) of approximately 2 µm with a fine particle fraction (FPF; particle size, <6.4 µm) between 45% and 52%. The MMAD and FPF did not change significantly after 6 months of storage (P > 0.05).


Assuntos
Broncodilatadores/análise , Fenoterol/administração & dosagem , Ipratrópio/análise , Inaladores Dosimetrados , Administração por Inalação , Aerossóis , Química Farmacêutica , Clorofluorcarbonetos de Metano , Estabilidade de Medicamentos , Armazenamento de Medicamentos , Desenho de Equipamento , Concentração de Íons de Hidrogênio , Tamanho da Partícula , Solventes
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