Continuous Cocrystallization for Dissolution Rate Optimization of a Poorly Water-Soluble Drug

被引:54
|
作者
Moradiya, Hiren [1 ]
Islam, Muhammad T. [1 ]
Woollam, Grahame R. [2 ]
Slipper, Ian J. [1 ]
Halsey, Sheelagh
Snowden, Martin J. [1 ]
Douroumis, D. [1 ]
机构
[1] Univ Greenwich, Fac Sci & Engn, Chatham ME4 4TB, Kent, England
[2] Novartis Pharma AG, Werk Klybeck, CH-4057 Basel, Switzerland
关键词
PHARMACEUTICAL CO-CRYSTALS; SOLID-STATE; CARBAMAZEPINE; FORMS;
D O I
10.1021/cg401375a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A continuous manufacturing process, hot melt extrusion (HME), was employed for the development of high quality carbamazepine-saccharin (CBZ-SCH) cocrystals. The produced cocrystals were compared with a prototype prepared by a solvent method. It was found that processing parameters such as temperature, screw speed, and screw configuration were the critical processing parameters. In-line near-infrared analysis demonstrated that cocrystallization takes place gradually during the process along the extruder's mixing zones. Further characterization of the extruded cocrystals proved that the manufactured highly crystalline cocrystals were similar to the prototype but had improved CBZ dissolution rates. Continuous manufacturing of cocrystals of water-insoluble drugs is a novel and robust approach.
引用
收藏
页码:189 / 198
页数:10
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