A fluidized-bed coating technology using near-critical carbon dioxide as fluidizing and drying medium

被引:11
作者
Niu, Fenghui [2 ]
Haslam, John [3 ]
Rajewski, Roger [4 ]
Subramaniam, Bala [1 ,2 ]
机构
[1] Univ Kansas, Dept Chem & Petr Engn, Lawrence, KS 66045 USA
[2] Univ Kansas, Ctr Environm Beneficial Catalysis, Lawrence, KS 66045 USA
[3] Univ Kansas, Biotechnol Innovat & Optimizat Ctr, Lawrence, KS 66045 USA
[4] Univ Kansas, Dept Pharmaceut Chem, Lawrence, KS 66045 USA
关键词
Coating; Fluidized bed; Polymers; Controlled release formulations; Near-critical carbon dioxide; ENCAPSULATION; PRESSURES; PARTICLES; AMBIENT; SOLIDS;
D O I
10.1016/j.supflu.2011.11.007
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A Wurster-type coater employing near-critical carbon dioxide as the fluidizing medium and antisolvent was developed for pharmaceutical applications. Suitably designed glass inserts housed in a high-pressure chamber allow for the controlled fluidization and circulation of the substrates with dense CO2. The CO2 also removes the solvent from the coating solution sprayed on the substrates, thereby precipitating the coating as a smooth layer. A variety of substrates were successfully coated with thin polymer films for aesthetic/handling purposes or for delayed release applications such as taste masking. The geometry of substrates include glass and microcrystalline cellulose (MCC) beads ranging in diameter from 0.5 to 2 mm, tablets up to 7.9 mm and cylindrical stents up to 20 mm in length. The demonstrated coating process expands the range of substrate/coating combinations possible with the conventional air-fluidized Wurster coater, making it feasible to coat water-soluble substrates with solutes sprayed from organic solutions at near-ambient temperatures wherein degradation of the active pharmaceutical ingredient is avoided. Coating with dense CO2 enables the use of traditional organic solvents with no risk of explosion. (c) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:315 / 320
页数:6
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