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Linear flow‐velocity gradient chromatography—An efficient method for increasing the process efficiency of batch and continuous capture chromatography of proteins
A new method was proposed for increasing the capture chromatography process efficiency, linear flow‐velocity gradient (LFG). The method uses a linear decreasing flow‐velocity gradient with time during the sample loading. The initial flow velocity, the final flow velocity and the gradient time are th...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986079/ https://www.ncbi.nlm.nih.gov/pubmed/33283261 http://dx.doi.org/10.1002/bit.27649 |
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author | Chen, Chyi‐Shin Ando, Kosei Yoshimoto, Noriko Yamamoto, Shuichi |
author_facet | Chen, Chyi‐Shin Ando, Kosei Yoshimoto, Noriko Yamamoto, Shuichi |
author_sort | Chen, Chyi‐Shin |
collection | PubMed |
description | A new method was proposed for increasing the capture chromatography process efficiency, linear flow‐velocity gradient (LFG). The method uses a linear decreasing flow‐velocity gradient with time during the sample loading. The initial flow velocity, the final flow velocity and the gradient time are the parameters to be tuned. We have developed a method for determining these parameters by using the total column capacity and the total loaded amount as a function of time. The capacity can be calculated by using the relationships between dynamic binding capacity (DBC) and residence time. By leveraging the capacity, loading amount, and the required conditions, the optimum LFG can be designed. The method was verified by ion‐exchange and protein A chromatography of monoclonal antibodies (mAbs). A two‐fold increase in the productivity during the sample loading was possible by LFG compared with the constant flow‐velocity (CF) operation. LFG was also applied to a 4‐column continuous process. The simulation showed that the cost of resin per unit amount of processed mAbs can be reduced by 13% while 1.4 times enhancement in productivity was preserved after optimization by LFG compared to CF. The process efficiency improvement is more pronounced when the isotherm is highly favorable and the loading volume is large. |
format | Online Article Text |
id | pubmed-7986079 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79860792021-03-25 Linear flow‐velocity gradient chromatography—An efficient method for increasing the process efficiency of batch and continuous capture chromatography of proteins Chen, Chyi‐Shin Ando, Kosei Yoshimoto, Noriko Yamamoto, Shuichi Biotechnol Bioeng ARTICLES A new method was proposed for increasing the capture chromatography process efficiency, linear flow‐velocity gradient (LFG). The method uses a linear decreasing flow‐velocity gradient with time during the sample loading. The initial flow velocity, the final flow velocity and the gradient time are the parameters to be tuned. We have developed a method for determining these parameters by using the total column capacity and the total loaded amount as a function of time. The capacity can be calculated by using the relationships between dynamic binding capacity (DBC) and residence time. By leveraging the capacity, loading amount, and the required conditions, the optimum LFG can be designed. The method was verified by ion‐exchange and protein A chromatography of monoclonal antibodies (mAbs). A two‐fold increase in the productivity during the sample loading was possible by LFG compared with the constant flow‐velocity (CF) operation. LFG was also applied to a 4‐column continuous process. The simulation showed that the cost of resin per unit amount of processed mAbs can be reduced by 13% while 1.4 times enhancement in productivity was preserved after optimization by LFG compared to CF. The process efficiency improvement is more pronounced when the isotherm is highly favorable and the loading volume is large. John Wiley and Sons Inc. 2021-01-03 2021-03 /pmc/articles/PMC7986079/ /pubmed/33283261 http://dx.doi.org/10.1002/bit.27649 Text en © 2020 The Authors. Biotechnology and Bioengineering Published by Wiley Periodicals LLC This is an open access article under the terms of the http://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 Chen, Chyi‐Shin Ando, Kosei Yoshimoto, Noriko Yamamoto, Shuichi Linear flow‐velocity gradient chromatography—An efficient method for increasing the process efficiency of batch and continuous capture chromatography of proteins |
title | Linear flow‐velocity gradient chromatography—An efficient method for increasing the process efficiency of batch and continuous capture chromatography of proteins |
title_full | Linear flow‐velocity gradient chromatography—An efficient method for increasing the process efficiency of batch and continuous capture chromatography of proteins |
title_fullStr | Linear flow‐velocity gradient chromatography—An efficient method for increasing the process efficiency of batch and continuous capture chromatography of proteins |
title_full_unstemmed | Linear flow‐velocity gradient chromatography—An efficient method for increasing the process efficiency of batch and continuous capture chromatography of proteins |
title_short | Linear flow‐velocity gradient chromatography—An efficient method for increasing the process efficiency of batch and continuous capture chromatography of proteins |
title_sort | linear flow‐velocity gradient chromatography—an efficient method for increasing the process efficiency of batch and continuous capture chromatography of proteins |
topic | ARTICLES |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7986079/ https://www.ncbi.nlm.nih.gov/pubmed/33283261 http://dx.doi.org/10.1002/bit.27649 |
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