Wilms Annika, Kleinebudde Peter
INVITE GmbH, Drug Delivery Innovation Center (DDIC), Chempark Building W32, 51368 Leverkusen, Germany.
Heinrich Heine University Düsseldorf, Institute of Pharmaceutics and Biopharmaceutics, Universitätsstraße 1, 40225 Düsseldorf, Germany.
Int J Pharm X. 2020 Nov 10;2:100059. doi: 10.1016/j.ijpx.2020.100059. eCollection 2020 Dec.
A key quality attribute for solid oral dosage forms is their hardness and ability to withstand breaking or grinding. If the product is to be manufactured continuously, it can be of interest to monitor the hardness of the material at different stages of manufacturing. Using the controlled process parameters of roll compaction/dry granulation specific compaction force, roll speed and gap width, hardness of the resulting ribbons and granules can be predicted. For the first time, in this study two yield variables (corrected torque of the granulation unit and throughput of material) are used to predict the granules failure load. The increase in granule hardness was monitored in-line when the specific compaction force was increased during the compaction process. This opens the way for in-line control of material hardness, and its use for feedback and feedforward control loops for future continuous manufacturing processes.
固体口服制剂的一个关键质量属性是其硬度以及承受破碎或研磨的能力。如果产品要连续生产,那么在制造的不同阶段监测材料的硬度可能会很有意义。利用辊压/干法制粒的受控工艺参数(比压实力、辊速和间隙宽度),可以预测所得带状物和颗粒的硬度。在本研究中,首次使用两个产量变量(制粒单元的校正扭矩和物料通量)来预测颗粒的破坏载荷。在压实过程中比压实力增加时,在线监测颗粒硬度的增加情况。这为材料硬度的在线控制以及将其用于未来连续制造过程的反馈和前馈控制回路开辟了道路。