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A Proposed Methodology for a Risk Assessment-Based Liposome Development Process

The requirements of a liposomal formulation vary depending on the pharmaceutical indication, the target patient population, and the corresponding route of administration. Different preparation methods require various material attributes (MAs) (properties and characteristics of the components) and pr...

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Publicado en:Pharmaceutics
Main Authors: Németh, Zsófia, Pallagi, Edina, Dobó, Dorina Gabriella, Csóka, Ildikó
Formato: Artigo
Idioma:Inglês
Publicado: MDPI 2020
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC7760874/
https://ncbi.nlm.nih.gov/pubmed/33260443
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/pharmaceutics12121164
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