Abstract

In view of growing interest and investment in continuous manufacturing, the development and utilization of mathematical model(s) of the manufacturing line is of prime importance. These models are essential for understanding the complex interplay between process-wide critical process parameters (CPPs) and critical quality attributes (CQAs) beyond the individual process operations. In this work, a flowsheet model that is an approximate representation of the ConsiGma TM -25 line for continuous tablet manufacturing, including wet granulation, is developed. The manufacturing line involves various unit operations, i.e., feeders, blenders, a twin-screw wet granulator, a fluidized bed dryer, a mill, and a tablet press. The unit operations are simulated using various modeling approaches such as data-driven models, semi-empirical models, population balance models, and mechanistic models. Intermediate feeders, blenders, and transfer lines between the units are also simulated. The continuous process is simulated using the flowsheet model thus developed and case studies are provided to demonstrate its application for dynamic simulation. Finally, the flowsheet model is used to systematically identify critical process parameters (CPPs) that affect process responses of interest using global sensitivity analysis methods. Liquid feed rate to the granulator, and air temperature and drying time in the dryer are identified as CPPs affecting the tablet properties.

Highlights

  • Flowsheet models are approximate mathematical representations of the manufacturing line.The incentives for flowsheet model development for the pharmaceutical industry have been described in the paper of Escotet-Espinoza et al [1]

  • Critical process parameters (CPPs) that affect product quality are identified through implementation of sensitivity analysis as explained in Sections 2.3 and 3.4

  • We focus on global sensitivity analysis as this is more relevant for pharmaceutical processes

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Summary

Introduction

The incentives for flowsheet model development for the pharmaceutical industry have been described in the paper of Escotet-Espinoza et al [1]. The first step in attaining these benefits is by the development of a flowsheet model that captures the relevant mechanisms for assessing the desired product properties as a function of process settings and material properties. This foundation built in this work, comprised of several diverse unit operation models that capture critical mechanisms, as a function of the process inputs

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