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Process Modeling and Simulation of Tableting—An Agent-Based Simulation Methodology for Direct Compression

In pharmaceutical manufacturing, the utmost aim is reliably producing high quality products. Simulation approaches allow virtual experiments of processes in the planning phase and the implementation of digital twins in operation. The industrial processing of active pharmaceutical ingredients (APIs)...

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Autores principales: Martin, Niels Lasse, Schomberg, Ann Kathrin, Finke, Jan Henrik, Abraham, Tim Gyung-min, Kwade, Arno, Herrmann, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308958/
https://www.ncbi.nlm.nih.gov/pubmed/34209261
http://dx.doi.org/10.3390/pharmaceutics13070996
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author Martin, Niels Lasse
Schomberg, Ann Kathrin
Finke, Jan Henrik
Abraham, Tim Gyung-min
Kwade, Arno
Herrmann, Christoph
author_facet Martin, Niels Lasse
Schomberg, Ann Kathrin
Finke, Jan Henrik
Abraham, Tim Gyung-min
Kwade, Arno
Herrmann, Christoph
author_sort Martin, Niels Lasse
collection PubMed
description In pharmaceutical manufacturing, the utmost aim is reliably producing high quality products. Simulation approaches allow virtual experiments of processes in the planning phase and the implementation of digital twins in operation. The industrial processing of active pharmaceutical ingredients (APIs) into tablets requires the combination of discrete and continuous sub-processes with complex interdependencies regarding the material structures and characteristics. The API and excipients are mixed, granulated if required, and subsequently tableted. Thereby, the structure as well as the properties of the intermediate and final product are influenced by the raw materials, the parametrized processes and environmental conditions, which are subject to certain fluctuations. In this study, for the first time, an agent-based simulation model is presented, which enables the prediction, tracking, and tracing of resulting structures and properties of the intermediates of an industrial tableting process. Therefore, the methodology for the identification and development of product and process agents in an agent-based simulation is shown. Implemented physical models describe the impact of process parameters on material structures. The tablet production with a pilot scale rotary press is experimentally characterized to provide calibration and validation data. Finally, the simulation results, predicting the final structures, are compared to the experimental data.
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spelling pubmed-83089582021-07-25 Process Modeling and Simulation of Tableting—An Agent-Based Simulation Methodology for Direct Compression Martin, Niels Lasse Schomberg, Ann Kathrin Finke, Jan Henrik Abraham, Tim Gyung-min Kwade, Arno Herrmann, Christoph Pharmaceutics Article In pharmaceutical manufacturing, the utmost aim is reliably producing high quality products. Simulation approaches allow virtual experiments of processes in the planning phase and the implementation of digital twins in operation. The industrial processing of active pharmaceutical ingredients (APIs) into tablets requires the combination of discrete and continuous sub-processes with complex interdependencies regarding the material structures and characteristics. The API and excipients are mixed, granulated if required, and subsequently tableted. Thereby, the structure as well as the properties of the intermediate and final product are influenced by the raw materials, the parametrized processes and environmental conditions, which are subject to certain fluctuations. In this study, for the first time, an agent-based simulation model is presented, which enables the prediction, tracking, and tracing of resulting structures and properties of the intermediates of an industrial tableting process. Therefore, the methodology for the identification and development of product and process agents in an agent-based simulation is shown. Implemented physical models describe the impact of process parameters on material structures. The tablet production with a pilot scale rotary press is experimentally characterized to provide calibration and validation data. Finally, the simulation results, predicting the final structures, are compared to the experimental data. MDPI 2021-06-30 /pmc/articles/PMC8308958/ /pubmed/34209261 http://dx.doi.org/10.3390/pharmaceutics13070996 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Martin, Niels Lasse
Schomberg, Ann Kathrin
Finke, Jan Henrik
Abraham, Tim Gyung-min
Kwade, Arno
Herrmann, Christoph
Process Modeling and Simulation of Tableting—An Agent-Based Simulation Methodology for Direct Compression
title Process Modeling and Simulation of Tableting—An Agent-Based Simulation Methodology for Direct Compression
title_full Process Modeling and Simulation of Tableting—An Agent-Based Simulation Methodology for Direct Compression
title_fullStr Process Modeling and Simulation of Tableting—An Agent-Based Simulation Methodology for Direct Compression
title_full_unstemmed Process Modeling and Simulation of Tableting—An Agent-Based Simulation Methodology for Direct Compression
title_short Process Modeling and Simulation of Tableting—An Agent-Based Simulation Methodology for Direct Compression
title_sort process modeling and simulation of tableting—an agent-based simulation methodology for direct compression
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8308958/
https://www.ncbi.nlm.nih.gov/pubmed/34209261
http://dx.doi.org/10.3390/pharmaceutics13070996
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