Ghent University, Laboratory of Pharmaceutical Process Analytical Technology, Ottergemsesteenweg 460, Gent 9000, Belgium; Ghent University, BIOMATH, Department of Data Analysis and Mathematical Modelling, Coupure Links 653, Gent 9000, Belgium.
Ghent University, Laboratory of Pharmaceutical Process Analytical Technology, Ottergemsesteenweg 460, Gent 9000, Belgium.
Int J Pharm. 2022 Jan 25;612:121284. doi: 10.1016/j.ijpharm.2021.121284. Epub 2021 Nov 20.
For continuous pharmaceutical manufacturing of oral solid dosages, it is essential that product quality is measured inline. In this application, a continuous rotary tablet press is used. The goal is a model-based assessment of the quality of the blend in the feed frame to determine whether the concentration of the active pharmaceutical ingredient (API) will be within the prescribed limits. This is to achieve a better quality assurance than by offline testing of a small sample of tablets. In this way, product quality for real-time release (RTR) could be implemented. With a near-infrared (NIR) probe, the concentration of the API in the feed chute and the feed-frame were measured, as well as the API concentration of the tablets by an offline NIR measurement. These different data sets are connected and used for the residence time distribution characterization of the mixing dynamic of the tablet press. A residence time distribution model is fitted to the data, and is further used to compute the lead-lag time. This yields information on how long it takes for a quantity of product to go from being measured in the feed frame until ending up in tablets. Further, it gives information on the occurrence of mixing in the feed-frame itself. These models allow making accurate predictions of whether tablets fall within specified concentration range in real-time. The real-time prediction can be used in combination with a control system both to maintain the quality of the blend as well as to know which tablets to discard. This real-time quality assurance will lead to less material waste and fewer declined batches of tablets.
对于连续的口服固体制剂制药生产,产品质量的在线测量至关重要。在本应用中,使用了连续旋转压片机。目标是基于模型评估进料架中混合物的质量,以确定活性药物成分 (API) 的浓度是否在规定范围内。这是为了通过对少量片剂进行离线测试来实现更好的质量保证。通过这种方式,可以实施实时放行 (RTR) 的产品质量。使用近红外 (NIR) 探头,测量了进料槽和进料架中 API 的浓度,以及离线 NIR 测量的片剂中 API 的浓度。这些不同的数据集被连接起来,并用于压片机混合动态的停留时间分布特性的描述。将停留时间分布模型拟合到数据中,并进一步用于计算滞后时间。这提供了有关产品从进料架中测量到最终进入片剂所需时间的信息。此外,它还提供了关于进料架本身混合发生的信息。这些模型允许对片剂是否实时落入指定浓度范围内进行准确预测。实时预测可与控制系统结合使用,以维持混合物的质量,并了解要丢弃哪些片剂。这种实时质量保证将导致更少的材料浪费和更少的片剂批次不合格。