| Literature DB >> 19040386 |
Dwayne T Friesen1, Ravi Shanker, Marshall Crew, Daniel T Smithey, W J Curatolo, J A S Nightingale.
Abstract
Spray-dried dispersions (SDDs) of low-solubility drugs have been prepared using the polymer hydroxypropyl methylcellulose acetate succinate (HPMCAS). For a variety of drug structures, these SDDs provide supersaturation in in vitro dissolution determinations and large bioavailability increases in vivo. In bile-salt/lecithin in vitro solutions, these SDDs provide amorphous drug/polymer colloids and an increased concentration of free drug and drug in micelles relative to crystalline or amorphous drug. As dry powders, the SDDs are a single amorphous phase in which the drug remains amorphous and dispersed and does not crystallize over storage times relevant for practical drug products. A melting temperature (Tm)/glass-transition temperature (Tg) (K/K) versus log P map for 139 compounds formulated as SDDs provides a perspective on an appropriate formulation strategy for low-solubility drugs with various physical properties.Entities:
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Year: 2008 PMID: 19040386 DOI: 10.1021/mp8000793
Source DB: PubMed Journal: Mol Pharm ISSN: 1543-8384 Impact factor: 4.939