Preformulation in Drug Product Design
Author:
Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-52520-9_3
Reference12 articles.
1. Arnott JA, Planey SL. The influence of lipophilicity in drug discovery and design. Expert Opin Drug Discovery. 2012;7(10):863–75.
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3. Huang S, Mao C, Williams RO III, Yang CY. Solubility advantage (and disadvantage) of pharmaceutical amorphous solid dispersions. J Pharm Sci. 2016;105(12):3549–61.
4. Jermain SV, Brough C, Williams RO III. Amorphous solid dispersions and nanocrystal technologies for poorly water-soluble drug delivery–an update. Int J Pharm. 2018;535(1–2):379–92.
5. Leleux J, Williams R. Recent advancements in mechanical reduction methods: particulate systems. Drug Dev Ind Pharm. 2014;40(3):289–300.
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