The effect of the drying temperature on the properties of wet-extruded calcium stearate pellets: Pellet microstructure, drug distribution, solid state and drug dissolution

被引:13
作者
Schrank, S. [1 ,2 ,3 ]
Kann, B. [4 ]
Saurugger, E. [2 ]
Hainschitz, M. [2 ]
Windbergs, M. [4 ,5 ,6 ]
Glasser, B. J. [7 ]
Khinast, J. [1 ,2 ]
Roblegg, E. [2 ,3 ]
机构
[1] Graz Univ Technol, Inst Proc & Particle Engn, A-8010 Graz, Austria
[2] Res Ctr Pharmaceut Engn GmbH, Graz, Austria
[3] Graz Univ, Dept Pharmaceut Technol, Inst Pharmaceut Sci, A-8010 Graz, Austria
[4] Univ Saarland, Dept Biopharmaceut & Pharmaceut Technol, D-66123 Saarbrucken, Germany
[5] Helmholtz Ctr Infect Res HZI, Saarbrucken, Germany
[6] Helmholtz Inst Pharmaceut Res Saarland HIPS, Dept Drug Delivery DDEL, Saarbrucken, Germany
[7] Rutgers State Univ, Dept Chem & Biochem Engn, Piscataway, NJ USA
关键词
Extrusion/spheronization; Ibuprofen; Differential scanning calorimetry; Infrared spectroscopy; Small and wide angle X-ray scattering; Raman imaging; MICROCRYSTALLINE CELLULOSE; EXTRUSION-SPHERONIZATION; ANHYDROUS THEOPHYLLINE; SUPPORTED CATALYSTS; RELEASE PROPERTIES; DELIVERY SYSTEMS; MELT EXTRUSION; PHASE-DIAGRAM; IBUPROFEN; BEHAVIOR;
D O I
10.1016/j.ijpharm.2014.12.030
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Although drying is widely applied during the manufacturing of solid dosage forms, its potential effect on the product's (key) properties is often underestimated. Hence, the present study addresses drying related modifications of wet-extruded pellets comprising calcium stearate (CaSt, matrix former) and ibuprofen (model drug). After spheronization, the pellets were tray dried at different temperatures. The dried pellets were evaluated regarding their microstructure, the ibuprofen distribution, solid state modifications and the resulting in-vitro dissolution profiles. The ibuprofen distribution profiles along the pellets' cross-sections varied for the different drying conditions. The profiles turned from inhomogeneous to uniform with increasing drying temperature. Temperatures above 20 degrees C yielded solid state modifications, including ibuprofen transition into the amorphous state and the formation of eutectic compositions. As none of the batches exhibited a high specific surface area associated with an open, well-interconnected pore system, the dissolution profiles were a function of the ibuprofen distribution. Differences in the solid state did not contribute to the dissolution behavior, since the CaSt matrix did not swell or dissolve in the dissolution medium. These findings show that drying may considerably affect the final product properties even for moderate drying conditions. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:779 / 787
页数:9
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