Laboratory of Pharmaceutical Process Analytical Technology, Ghent University, Ghent, Belgium.
Eur J Pharm Biopharm. 2012 Oct;82(2):429-36. doi: 10.1016/j.ejpb.2012.07.017. Epub 2012 Aug 7.
Manufacturers of pharmaceutical solid dosage forms aim for a reduced production time and a shorter "time-to-market." Therefore, continuous manufacturing gains increasing interest in the pharmaceutical industry. For continuous manufacturing, the quality of produced pharmaceuticals should be assessed in real-time (in-line, on-line, and at-line) and not via the traditional off-line, often destructive and time-consuming analysis methods that supply the desired information only hours after sampling. This research paper evaluates three Process Analytical Technology (PAT) tools for the real-time at-line analysis of granules, which were produced using a continuous wet twin-screw granulator being part of a from powder-to-tablet production line (ConsiGma™-25). A Raman and NIR spectrometer were used together with a photometric imaging technique in order to acquire solid-state information and granule size data. These multivariate data were then used to predict the granules' moisture content, tapped and bulk density, and flowability. The three PAT tools provided complementary information for predicting these quality attributes of the continuously produced granules. The residual moisture content was mostly correlated with the spectroscopic data, whereas the imaging data had the highest predictive capability for the flowability of the granules.
制药固体制剂制造商的目标是缩短生产时间和“上市时间”。因此,连续制造在制药行业中的关注度日益增加。对于连续制造,应实时(在线、离线和在线)评估所生产药品的质量,而不是通过传统的离线、通常具有破坏性且耗时的分析方法,这些方法只能在采样数小时后提供所需信息。本文评估了三种过程分析技术 (PAT) 工具,用于实时分析使用连续湿双螺杆造粒机(ConsiGma™-25)生产的颗粒。拉曼和近红外光谱仪与光度成像技术一起使用,以获取固态信息和颗粒尺寸数据。然后,使用这些多元数据来预测颗粒的水分含量、振实和堆积密度以及流动性。这三种 PAT 工具为预测连续生产颗粒的这些质量特性提供了互补信息。残余水分含量主要与光谱数据相关,而成像数据对颗粒的流动性具有最高的预测能力。