Solid Dispersions of Poorly Water Soluble Drug

被引:0
|
作者
Gruberova, Lucie [1 ]
Kratochvil, Bohumil [1 ]
机构
[1] Vysoka Skola Chem Technol Praze, Ustav Chem Pevnych Latek, Tech 5, Prague 16628 6, Czech Republic
来源
CHEMICKE LISTY | 2019年 / 113卷 / 06期
关键词
crystalline/amorphous solid dispersions; solid solution; solid suspension; poorly water soluble drugs; carrier-controlled/drug-controlled dissolution; melting method; solvent method; INCREASING DISSOLUTION RATES; GASTROINTESTINAL ABSORPTION; EUTECTIC MIXTURES; IN-VITRO; BIOAVAILABILITY; RELEASE; BEHAVIOR; STABILIZATION; FORMULATION; SOLUBILITY;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
There has been a great interest in solid dispersions since 60's because it is one of the most promising methods to increase the low bioavailability of poorly water soluble drugs. Numerous studies on solid dispersions have been published, showing advantages of these materials. The main benefits of solid dispersions for low soluble drugs lie in the possibility to reduce the particle size, even to molecular level, to enhance wettability and porosity, as well as to change the drug crystalline state, preferably into amorphous state. Despite high research interests, the number of marketed products with solid dispersion is surprisingly low. The aim of this review is to provide basic information for better understanding of solid dispersions. The article contains definitions and characterization of the various system including four generations of solid dispersions, description of preparation methods and mechanisms of drug dissolution.
引用
收藏
页码:383 / 390
页数:8
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