Design of Freeze-Drying Processes for Pharmaceuticals: Practical Advice
By X. Tang, M. Pikal. Pharmaceutical Research, 2004
927 citations recorded by the source corpus.
Subfields: Materials Chemistry, Molecular Biology
View Paper: https://www.semanticscholar.org/paper/94f25bf642ffaa8590fe40618cf24f48078ae44d
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In Materials Chemistry
In Molecular Biology
Citations in the corpus
- Freeze-drying of nanoparticles: formulation, process and storage considerations. (2006, background): “Generally, freezing must be carried out below Tg′ of a frozen amorphous sample or below Teu (eutectic crystallization temperature) which is the crystallization temperature of soluble component as a mixture with ice, if it is in a crystalline state in order to ensure the total solidification of the s”
- Formulation and manufacturability of biologics. (2009, methodology): “The literature is replete with examples on formulation development using such processes [41 ,42–50].”