Current Trends on Solid Dispersions: Past, Present, and Future

被引:21
|
作者
Malkawi, Ruba [1 ]
Malkawi, Walla I. I. [2 ]
Al-Mahmoud, Yahia [1 ]
Tawalbeh, Jawad [3 ]
机构
[1] Jadara Univ, Sch Pharm, POB 733, Irbid 21110, Jordan
[2] Iowa State Univ, Sch Pharm, Ames, IA 50011 USA
[3] Teesside Univ, Sch Business, Campus Heart, Southfield Rd, Middlesbrough TS1 3BX, England
关键词
WATER-SOLUBLE DRUGS; HOT-MELT EXTRUSION; IN-VIVO EVALUATION; ORAL BIOAVAILABILITY; DISSOLUTION RATE; SOLUBILITY ENHANCEMENT; SOLVENT EVAPORATION; CYCLODEXTRIN COMPLEXES; ANTIOXIDANT ACTIVITY; VITRO;
D O I
10.1155/2022/5916013
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Solid dispersions have achieved significant interest as an effective means of enhancing the dissolution rate and thus the bioavailability of a range of weakly water-soluble drugs. Solid dispersions of weakly water-soluble drugs with water-soluble carriers have lowered the frequency of these problems and improved dissolution. Solid dispersion is a solubilization technology emphasizing mainly on, drug-polymer two-component systems in which drug dispersion and its stabilization is the key to formulation development. Therefore, this technology is recognized as an exceptionally useful means of improving the dissolution properties of poorly water-soluble drugs and in the latest years, a big deal of understanding has been accumulated about solid dispersion, however, their commercial application is limited. In this review article, emphasis is placed on solubility, BCS classification, and carriers. Moreover, this article presents the diverse preparation techniques for solid dispersion and gathers some of the recent technological transfers. The different types of solid dispersions based on the carrier used and molecular arrangement were underlined. Additionally, it summarizes the mechanisms, the methods of preparing solid dispersions, and the marketed drugs that are available using solid dispersion approaches.
引用
收藏
页数:17
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