Casas-Orozco Daniel, Laky Daniel, Wang Vivian, Abdi Mesfin, Feng X, Wood E, Reklaitis Gintaras V, Nagy Zoltan K
Davidson School of Chemical Engineering, Purdue University, West Lafayette, IN 47906, USA.
Office of Pharmaceutical Quality, Center for Drug Evaluation and Research, Food & Drug Administration, Silver Spring, MD, USA.
AIChE J. 2023;69(9). doi: 10.1002/aic.18142. Epub 2023 Apr 16.
Increased interest in the pharmaceutical industry to transition from batch to continuouos manufacturing motivates the use of digital frameworks that allow systematic comparison of candidate process configurations. This paper evaluates the technical and economic feasibility of different end-to-end optimal process configurations, . batch, hybrid and continuous, for small-scale manufacturing of an active pharmaceutical ingredient. Production were analyzed for those configurations containing continuous equipment, where significant start-up effects are expected given the relatively short campaign times considered. Hybrid operating mode was found to be the most attractive process configuration at intermediate and large annual production targets, which stems from combining continuous reactors and semi-batch vaporization equipment. Continuous operation was found to be more costly, due to long stabilization times of continuous crystallization, and thermodynamic limitations of flash vaporization. Our work reveals the benefits of systematic digital evaluation of process configurations that operate under feasible conditions and compliant product quality attributes.
制药行业对从间歇式生产向连续式生产转型的兴趣日益浓厚,这推动了数字框架的使用,该框架允许对候选工艺配置进行系统比较。本文评估了用于活性药物成分小规模生产的不同端到端最优工艺配置(间歇式、混合式和连续式)的技术和经济可行性。对那些包含连续设备的配置进行了生产分析,考虑到所考虑的相对较短的生产周期,预计会有显著的启动效应。发现混合操作模式在中等和大型年度生产目标下是最具吸引力的工艺配置,这源于连续反应器和半间歇式汽化设备的结合。由于连续结晶的稳定时间长以及闪蒸汽化的热力学限制,连续操作成本更高。我们的工作揭示了对在可行条件下运行且符合产品质量属性的工艺配置进行系统数字评估的好处。