Monteyne Tinne, Heeze Liza, Mortier Severine Therese F C, Oldörp Klaus, Cardinaels Ruth, Nopens Ingmar, Vervaet Chris, Remon Jean-Paul, De Beer Thomas
Laboratory of Pharmaceutical Process Analytical Technology Department of Pharmaceutical Analysis, Faculty of Pharmaceutical Sciences, Ghent University, Ottergemsesteenweg 460, 9000, Ghent, Belgium.
BIOMATH, Department of Mathematical Modelling, Statistics and Bioinformatics, Faculty of Bioscience Engineering, Ghent University, Coupure Links 653,, 9000, Ghent, Belgium.
Pharm Res. 2016 Oct;33(10):2481-94. doi: 10.1007/s11095-016-1973-6. Epub 2016 Jun 22.
Twin screw hot melt granulation (TS HMG) is a valuable, but still unexplored alternative to continuous granulation of moisture sensitive drugs. However, knowledge of the material behavior during TS HMG is crucial to optimize the formulation, process and resulting granule properties. The aim of this study was to evaluate the agglomeration mechanism during TS HMG using a rheometer in combination with differential scanning calorimetry (DSC).
An immiscible drug-binder formulation (caffeine-Soluplus(®)) was granulated via TS HMG in combination with thermal and rheological analysis (conventional and Rheoscope), granule characterization and Near Infrared chemical imaging (NIR-CI).
A thin binder layer with restricted mobility was formed on the surface of the drug particles during granulation and is covered by a second layer with improved mobility when the Soluplus(®) concentration exceeded 15% (w/w). The formation of this second layer was facilitated at elevated granulation temperatures and resulted in smaller and more spherical granules.
The combination of thermal and rheological analysis and NIR-CI images was advantageous to develop in-depth understanding of the agglomeration mechanism during continuous TS HMG and provided insight in the granule properties as function of process temperature and binder concentration.
双螺杆热熔制粒(TS HMG)是对湿度敏感药物进行连续制粒的一种有价值但仍未被充分探索的替代方法。然而,了解TS HMG过程中的物料行为对于优化配方、工艺及最终颗粒性质至关重要。本研究的目的是结合流变仪和差示扫描量热法(DSC)评估TS HMG过程中的团聚机制。
通过TS HMG结合热分析和流变分析(传统方法和流变仪)、颗粒表征及近红外化学成像(NIR-CI)对不相容的药物-粘合剂配方(咖啡因-聚乙烯己内酰胺(Soluplus®))进行制粒。
制粒过程中,药物颗粒表面形成了一层流动性受限的薄粘合剂层,当Soluplus®浓度超过15%(w/w)时,该层被一层流动性更好的第二层覆盖。在较高的制粒温度下,第二层的形成更容易,从而得到更小、更球形的颗粒。
热分析和流变分析与NIR-CI图像相结合,有利于深入了解连续TS HMG过程中的团聚机制,并能深入了解颗粒性质与工艺温度和粘合剂浓度之间的关系。