Ryckaert Alexander, Ghijs Michael, Portier Christoph, Djuric Dejan, Funke Adrian, Vervaet Chris, De Beer Thomas
Laboratory of Pharmaceutical Process Analytical Technology, Department of Pharmaceutical Analysis, Ghent University, Ottergemsesteenweg 460, 9000 Ghent, Belgium.
BIOMATH, Department of Mathematical Modelling, Statistics and Bio-informatics, Ghent University, Coupure Links 653, 9000 Ghent, Belgium.
Pharmaceutics. 2021 Feb 23;13(2):293. doi: 10.3390/pharmaceutics13020293.
The drying unit of a continuous from-powder-to-tablet manufacturing line based on twin-screw granulation (TSG) is a crucial intermediate process step to achieve the desired tablet quality. Understanding the size reduction of pharmaceutical granules before, during, and after the fluid bed drying process is, however, still lacking. A first major goal was to investigate the breakage and attrition phenomena during transport of wet and dry granules, the filling phase, and drying phase on a ConsiGma-25 system (C25). Pneumatic transport of the wet granules after TSG towards the dryer induced extensive breakage, whereas the turbulent filling and drying phase of the drying cells caused rather moderate breakage and attrition. Subsequently, the dry transfer line was responsible for additional extensive breakage and attrition. The second major goal was to compare the influence of drying air temperature and drying time on granule size and moisture content for granules processed with a commercial-scale ConsiGma-25 system and with the R&D-scale ConsiGma-1 (C1) system. Generally, the granule quality obtained after drying with C1 was not predictive for the C25, making it challenging during process development with the C1 to obtain representative granules for the C25.
基于双螺杆制粒(TSG)的连续式从粉末到片剂生产线的干燥单元,是实现理想片剂质量的关键中间工艺步骤。然而,目前仍缺乏对流化床干燥过程之前、期间和之后药物颗粒尺寸减小情况的了解。第一个主要目标是研究在ConsiGma-25系统(C25)上湿颗粒和干颗粒运输、填充阶段及干燥阶段的破碎和磨损现象。双螺杆制粒后湿颗粒向干燥器的气力输送会导致大量破碎,而干燥单元的湍流填充和干燥阶段造成的破碎和磨损则较为适度。随后,干燥后的传输线导致了额外的大量破碎和磨损。第二个主要目标是比较使用商业规模的ConsiGma-25系统和研发规模的ConsiGma-1(C1)系统处理的颗粒,干燥空气温度和干燥时间对颗粒尺寸和水分含量的影响。一般来说,用C1干燥后获得的颗粒质量无法预测C25的情况,这使得在使用C1进行工艺开发时,很难获得能代表C25的颗粒。