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Technology transfer of a monitoring system to predict product concentration and purity of biopharmaceuticals in real‐time during chromatographic separation

Technological developments require the transfer to their location of application to make use of them. We describe the transfer of a real‐time monitoring system for lab‐scale preparative chromatography to two new sites where it will be used and developed further. Equivalent equipment was used. The ca...

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Autores principales: Christler, Anna, Scharl, Theresa, Sauer, Dominik G., Köppl, Johannes, Tscheließnig, Anne, Toy, Cabir, Melcher, Michael, Jungbauer, Alois, Dürauer, Astrid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518415/
https://www.ncbi.nlm.nih.gov/pubmed/34170524
http://dx.doi.org/10.1002/bit.27870
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author Christler, Anna
Scharl, Theresa
Sauer, Dominik G.
Köppl, Johannes
Tscheließnig, Anne
Toy, Cabir
Melcher, Michael
Jungbauer, Alois
Dürauer, Astrid
author_facet Christler, Anna
Scharl, Theresa
Sauer, Dominik G.
Köppl, Johannes
Tscheließnig, Anne
Toy, Cabir
Melcher, Michael
Jungbauer, Alois
Dürauer, Astrid
author_sort Christler, Anna
collection PubMed
description Technological developments require the transfer to their location of application to make use of them. We describe the transfer of a real‐time monitoring system for lab‐scale preparative chromatography to two new sites where it will be used and developed further. Equivalent equipment was used. The capture of a biopharmaceutical model protein, human fibroblast growth factor 2 (FGF‐2) was used to evaluate the system transfer. Predictive models for five quality attributes based on partial least squares regression were transferred. Six out of seven online sensors (UV/VIS, pH, conductivity, IR, RI, and MALS) showed comparable signals between the sites while one sensor (fluorescence) showed different signal profiles. A direct transfer of the models for real‐time monitoring was not possible, mainly due to differences in sensor signals. Adaptation of the models was necessary. Then, among five prediction models, the prediction errors of the test run at the new sites were on average twice as high as at the training site (model‐wise 0.9–5.7 times). Additionally, new prediction models for different products were trained at each new site. These allowed monitoring the critical quality attributes of two new biopharmaceutical products during their purification processes with mean relative deviations between 1% and 33%.
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spelling pubmed-85184152021-10-21 Technology transfer of a monitoring system to predict product concentration and purity of biopharmaceuticals in real‐time during chromatographic separation Christler, Anna Scharl, Theresa Sauer, Dominik G. Köppl, Johannes Tscheließnig, Anne Toy, Cabir Melcher, Michael Jungbauer, Alois Dürauer, Astrid Biotechnol Bioeng ARTICLES Technological developments require the transfer to their location of application to make use of them. We describe the transfer of a real‐time monitoring system for lab‐scale preparative chromatography to two new sites where it will be used and developed further. Equivalent equipment was used. The capture of a biopharmaceutical model protein, human fibroblast growth factor 2 (FGF‐2) was used to evaluate the system transfer. Predictive models for five quality attributes based on partial least squares regression were transferred. Six out of seven online sensors (UV/VIS, pH, conductivity, IR, RI, and MALS) showed comparable signals between the sites while one sensor (fluorescence) showed different signal profiles. A direct transfer of the models for real‐time monitoring was not possible, mainly due to differences in sensor signals. Adaptation of the models was necessary. Then, among five prediction models, the prediction errors of the test run at the new sites were on average twice as high as at the training site (model‐wise 0.9–5.7 times). Additionally, new prediction models for different products were trained at each new site. These allowed monitoring the critical quality attributes of two new biopharmaceutical products during their purification processes with mean relative deviations between 1% and 33%. John Wiley and Sons Inc. 2021-07-03 2021-10 /pmc/articles/PMC8518415/ /pubmed/34170524 http://dx.doi.org/10.1002/bit.27870 Text en © 2021 The Authors. Biotechnology and Bioengineering Published by Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle ARTICLES
Christler, Anna
Scharl, Theresa
Sauer, Dominik G.
Köppl, Johannes
Tscheließnig, Anne
Toy, Cabir
Melcher, Michael
Jungbauer, Alois
Dürauer, Astrid
Technology transfer of a monitoring system to predict product concentration and purity of biopharmaceuticals in real‐time during chromatographic separation
title Technology transfer of a monitoring system to predict product concentration and purity of biopharmaceuticals in real‐time during chromatographic separation
title_full Technology transfer of a monitoring system to predict product concentration and purity of biopharmaceuticals in real‐time during chromatographic separation
title_fullStr Technology transfer of a monitoring system to predict product concentration and purity of biopharmaceuticals in real‐time during chromatographic separation
title_full_unstemmed Technology transfer of a monitoring system to predict product concentration and purity of biopharmaceuticals in real‐time during chromatographic separation
title_short Technology transfer of a monitoring system to predict product concentration and purity of biopharmaceuticals in real‐time during chromatographic separation
title_sort technology transfer of a monitoring system to predict product concentration and purity of biopharmaceuticals in real‐time during chromatographic separation
topic ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518415/
https://www.ncbi.nlm.nih.gov/pubmed/34170524
http://dx.doi.org/10.1002/bit.27870
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