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AAPS PharmSciTech ; 9(2): 620-7, 2008.
Artículo en Inglés | MEDLINE | ID: mdl-18459048

RESUMEN

The purpose of this paper was to develop a statistical methodology to optimize tablet manufacturing considering drug chemical and physical properties applying a crossed experimental design. The assessed model drug was dried ferrous sulphate and the variables were the hardness and the relative proportions of three excipients, binder, filler and disintegrant. Granule properties were modeled as a function of excipient proportions and tablet parameters were defined by the excipient proportion and hardness. The desirability function was applied to achieve optimal values for excipient proportions and hardness. In conclusion, crossed experimental design using hardness as the only process variable is an efficient strategy to quickly determine the optimal design process for tablet manufacturing. This method can be applied for any tablet manufacturing method.


Asunto(s)
Excipientes/química , Compuestos Ferrosos/química , Modelos Estadísticos , Tecnología Farmacéutica/métodos , Celulosa/química , Química Farmacéutica , Dureza , Tamaño de la Partícula , Povidona/química , Polvos , Almidón/análogos & derivados , Almidón/química , Ácidos Esteáricos/química , Comprimidos , Factores de Tiempo
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