Fast-Dissolving Solid Dispersions for the Controlled Release of Poorly Watersoluble Drugs
Author:
Affiliation:
1. Deakin University, School of Medicine, Geelong,Australia
2. College of Pharmacy, Ajou University, Suwon,Korea
3. Department for Management of Science and Technology Development, Ton Duc Thang University, Ho Chi Minh City,Vietnam
Abstract
Publisher
Bentham Science Publishers Ltd.
Subject
Drug Discovery,Pharmacology
Reference111 articles.
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3. Morgen M.; Saxena A.; Chen X-Q.; Miller W.; Nkansah R.; Goodwin A.; Cape J.; Haskell R.; Su C.; Gudmundsson O.; Hageman M.; Kumar A.; Chowan G.S.; Rao A.; Holenarsipur V.K.; Lipophilic salts of poorly soluble compounds to enable high-dose lipidic SEDDS formulations in drug discovery. Eur J Pharm Biopharm 2017,117,212-223
4. Alsenz J.; Kansy M.; High throughput solubility measurement in drug discovery and development. Adv Drug Deliv Rev 2007,59(7),546-567
5. Kuentz M.; Imanidis G.; In silico prediction of the solubility advantage for amorphous drugs - Are there property-based rules for drug discovery and early pharmaceutical development? Eur J Pharm Sci 2013,48(3),554-562
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