Tian Geng, Koolivand Abdollah, Gu Zongyu, Orella Michael, Shaw Ryan, O'Connor Thomas F
Office of Pharmaceutical Quality, Center for Drug Evaluation Research, Food and Drug Administration, 10903 New Hampshire Ave, Silver Spring, Maryland, 20993, USA.
Department of Chemical Engineering, Massachusetts Institute of Technology, 25 Ames Street, Cambridge, Massachusetts, 02139, USA.
AAPS PharmSciTech. 2021 Jan 5;22(1):25. doi: 10.1208/s12249-020-01913-8.
Continuous manufacturing (CM) is an emerging technology which can improve pharmaceutical manufacturing and reduce drug product quality issues. One challenge that needs to be addressed when adopting CM technology is material traceability through the entire continuous process, which constitutes one key aspect of control strategy. Residence time distribution (RTD) plays an important role in material traceability as it characterizes the material spreading through the process. The propagation of upstream disturbances could be predictively tracked through the entire process by convolution of the disturbance and the RTD. The present study sets up the RTD-based modeling framework in a commonly used process modeling environment, gPROMS, and integrates it with existing modules and built-in tools (e.g., parameter estimation). Concentration calculations based on the convolution integral requires access to historical stream property information, which is not readily available in flowsheet modeling platforms. Thus, a novel approach is taken whereby a partial differential equation is used to propagate and store historical data as the simulation marches forward in time. Other stream properties not modeled by an RTD are determined in auxiliary modules. To illustrate the application of the framework, an integrated RTD-auxiliary model for a continuous direct compression manufacturing line was developed. An excellent agreement was found between the model predictions and experiments. The validated model was subsequently used to assess in-process control strategies for feeder and material traceability through the process. Our simulation results show that the employed modeling approach facilitates risk-based assessment of the continuous line by promoting our understanding on the process.
连续制造(CM)是一种新兴技术,它可以改善药品生产并减少药品质量问题。采用CM技术时需要解决的一个挑战是在整个连续过程中的物料可追溯性,这是控制策略的一个关键方面。停留时间分布(RTD)在物料可追溯性中起着重要作用,因为它表征了物料在整个过程中的扩散情况。通过将干扰与RTD进行卷积,可以在整个过程中预测性地跟踪上游干扰的传播。本研究在常用的过程建模环境gPROMS中建立了基于RTD的建模框架,并将其与现有模块和内置工具(如参数估计)集成。基于卷积积分的浓度计算需要访问历史物流属性信息,而这在流程图建模平台中不易获得。因此,采用了一种新颖的方法,即使用偏微分方程随着模拟时间的推进来传播和存储历史数据。未由RTD建模的其他物流属性在辅助模块中确定。为了说明该框架的应用,开发了一个用于连续直接压片生产线的集成RTD-辅助模型。模型预测与实验结果之间发现了极好的一致性。随后,使用经过验证的模型来评估进料器的过程控制策略以及整个过程中的物料可追溯性。我们的模拟结果表明,所采用的建模方法通过增进我们对过程的理解,促进了对连续生产线基于风险的评估。