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J Pharm Sci ; 112(1): 264-271, 2023 01.
Artigo em Inglês | MEDLINE | ID: mdl-36270539

RESUMO

Quality control is of critical importance in manufacturing of lyophilized drug product, which is accomplished by monitoring the process parameters. The residual gas analyzer has emerged as a useful tool in determination of endpoint for primary and secondary drying in lyophilization process as well as leak detection in vacuum systems. This study presents the application of in situ RGA to quantify outgassing rates of species released from aqueous inorganic and organic ammonium salt formulations throughout the freeze-drying process. The determination of ammonia outgassing conditions aids in ensuring product quality where ammonia release is an indication for loss of co-solvent or degradation of active pharmaceutical ingredients (APIs). Data analysis methods are developed to determine ammonia presence under various process conditions. In-situ real time monitoring of vapor dynamics enables RGA to be used as a tool to characterize counter-ion loss throughout the freeze-drying cycle.


Assuntos
Compostos de Amônio , Química Farmacêutica , Química Farmacêutica/métodos , Amônia , Liofilização/métodos , Composição de Medicamentos/métodos , Gases , Temperatura
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