Process Design of Continuous Powder Blending Using Residence Time Distribution and Feeding Models

The present paper reports a thorough continuous powder blending process design of acetylsalicylic acid (ASA) and microcrystalline cellulose (MCC) based on the Process Analytical Technology (PAT) guideline. A NIR-based method was applied using multivariate data analysis to achieve in-line process monitoring. The process dynamics were described with residence time distribution (RTD) models to achieve deep process understanding. The RTD was determined using the active pharmaceutical ingredient (API) as a tracer with multiple designs of experiment (DoE) studies to determine the effect of critical process parameters (CPPs) on the process dynamics. To achieve quality control through material diversion from feeding data, soft sensor-based process control tools were designed using the RTD model. The operation block model of the system was designed to select feasible experimental setups using the RTD model, and feeder characterizations as digital twins, therefore visualizing the output of theoretical setups. The concept significantly reduces the material and instrumental costs of process design and implementation.

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or continue reading here: Gyürkés, M.; Madarász, L.; Köte, Á.; Domokos, A.; Mészáros, D.; Beke, Á.K.; Nagy, B.; Marosi, G.; Pataki, H.; Nagy, Z.K.; Farkas, A. Process Design of Continuous Powder Blending Using Residence Time Distribution and Feeding Models. Pharmaceutics 2020, 12, 1119.

Keywords: residence time distribution; continuous powder blending; operation block model; feeder selection; funnel plot; Acetylsalicylic acid (ASA), microcrystalline cellulose (MCC, Vivapur® 200)

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