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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 mon...

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Autores principales: Gyürkés, Martin, Madarász, Lajos, Köte, Ákos, Domokos, András, Mészáros, Dániel, Beke, Áron Kristóf, Nagy, Brigitta, Marosi, György, Pataki, Hajnalka, Nagy, Zsombor Kristóf, Farkas, Attila
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7699818/
https://www.ncbi.nlm.nih.gov/pubmed/33233635
http://dx.doi.org/10.3390/pharmaceutics12111119
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author Gyürkés, Martin
Madarász, Lajos
Köte, Ákos
Domokos, András
Mészáros, Dániel
Beke, Áron Kristóf
Nagy, Brigitta
Marosi, György
Pataki, Hajnalka
Nagy, Zsombor Kristóf
Farkas, Attila
author_facet Gyürkés, Martin
Madarász, Lajos
Köte, Ákos
Domokos, András
Mészáros, Dániel
Beke, Áron Kristóf
Nagy, Brigitta
Marosi, György
Pataki, Hajnalka
Nagy, Zsombor Kristóf
Farkas, Attila
author_sort Gyürkés, Martin
collection PubMed
description 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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spelling pubmed-76998182020-11-29 Process Design of Continuous Powder Blending Using Residence Time Distribution and Feeding Models Gyürkés, Martin Madarász, Lajos Köte, Ákos Domokos, András Mészáros, Dániel Beke, Áron Kristóf Nagy, Brigitta Marosi, György Pataki, Hajnalka Nagy, Zsombor Kristóf Farkas, Attila Pharmaceutics Article 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. MDPI 2020-11-20 /pmc/articles/PMC7699818/ /pubmed/33233635 http://dx.doi.org/10.3390/pharmaceutics12111119 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gyürkés, Martin
Madarász, Lajos
Köte, Ákos
Domokos, András
Mészáros, Dániel
Beke, Áron Kristóf
Nagy, Brigitta
Marosi, György
Pataki, Hajnalka
Nagy, Zsombor Kristóf
Farkas, Attila
Process Design of Continuous Powder Blending Using Residence Time Distribution and Feeding Models
title Process Design of Continuous Powder Blending Using Residence Time Distribution and Feeding Models
title_full Process Design of Continuous Powder Blending Using Residence Time Distribution and Feeding Models
title_fullStr Process Design of Continuous Powder Blending Using Residence Time Distribution and Feeding Models
title_full_unstemmed Process Design of Continuous Powder Blending Using Residence Time Distribution and Feeding Models
title_short Process Design of Continuous Powder Blending Using Residence Time Distribution and Feeding Models
title_sort process design of continuous powder blending using residence time distribution and feeding models
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7699818/
https://www.ncbi.nlm.nih.gov/pubmed/33233635
http://dx.doi.org/10.3390/pharmaceutics12111119
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