无定形固体
过饱和度
喷雾干燥
生物利用度
胶束
聚合物
材料科学
化学
化学工程
溶解
玻璃化转变
色谱法
差示扫描量热法
溶解度
结晶
溶解试验
有机化学
结晶度
作者
Dwayne Thomas Friesen,Ravi Mysore Shanker,Marshall David Crew,Daniel Tod Smithey,W. J. Curatolo,James Alan Schriver Nightingale
摘要
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.
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