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The design basis for the integrated and continuous biomanufacturing framework

An 8 ton per year manufacturing facility is described based on the framework for integrated and continuous bioprocessing (ICB) common to all known biopharmaceutical implementations. While the output of this plant rivals some of the largest fed‐batch plants in the world, the equipment inside the plan...

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Autores principales: Coffman, Jon, Bibbo, Kenneth, Brower, Mark, Forbes, Robert, Guros, Nicholas, Horowski, Brian, Lu, Rick, Mahajan, Rajiv, Patil, Ujwal, Rose, Steven, Shultz, Joseph
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/PMC8453788/
https://www.ncbi.nlm.nih.gov/pubmed/33522595
http://dx.doi.org/10.1002/bit.27697
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author Coffman, Jon
Bibbo, Kenneth
Brower, Mark
Forbes, Robert
Guros, Nicholas
Horowski, Brian
Lu, Rick
Mahajan, Rajiv
Patil, Ujwal
Rose, Steven
Shultz, Joseph
author_facet Coffman, Jon
Bibbo, Kenneth
Brower, Mark
Forbes, Robert
Guros, Nicholas
Horowski, Brian
Lu, Rick
Mahajan, Rajiv
Patil, Ujwal
Rose, Steven
Shultz, Joseph
author_sort Coffman, Jon
collection PubMed
description An 8 ton per year manufacturing facility is described based on the framework for integrated and continuous bioprocessing (ICB) common to all known biopharmaceutical implementations. While the output of this plant rivals some of the largest fed‐batch plants in the world, the equipment inside the plant is relatively small: the plant consists of four 2000 L single‐use bioreactors and has a maximum flow rate of 13 L/min. The equipment and facility for the ICB framework is described in sufficient detail to allow biopharmaceutical companies, vendors, contract manufacturers to build or buy their own systems. The design will allow the creation of a global ICB ecosystem that will transform biopharmaceutical manufacturing. The design is fully backward compatible with legacy fed‐batch processes. A clinical production scale is described that can produce smaller batch sizes with the same equipment as that used at the commercial scale. The design described allows the production of as little as 10 g to nearly 35 kg of drug substance per day.
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spelling pubmed-84537882021-09-27 The design basis for the integrated and continuous biomanufacturing framework Coffman, Jon Bibbo, Kenneth Brower, Mark Forbes, Robert Guros, Nicholas Horowski, Brian Lu, Rick Mahajan, Rajiv Patil, Ujwal Rose, Steven Shultz, Joseph Biotechnol Bioeng ARTICLES An 8 ton per year manufacturing facility is described based on the framework for integrated and continuous bioprocessing (ICB) common to all known biopharmaceutical implementations. While the output of this plant rivals some of the largest fed‐batch plants in the world, the equipment inside the plant is relatively small: the plant consists of four 2000 L single‐use bioreactors and has a maximum flow rate of 13 L/min. The equipment and facility for the ICB framework is described in sufficient detail to allow biopharmaceutical companies, vendors, contract manufacturers to build or buy their own systems. The design will allow the creation of a global ICB ecosystem that will transform biopharmaceutical manufacturing. The design is fully backward compatible with legacy fed‐batch processes. A clinical production scale is described that can produce smaller batch sizes with the same equipment as that used at the commercial scale. The design described allows the production of as little as 10 g to nearly 35 kg of drug substance per day. John Wiley and Sons Inc. 2021-05-11 2021-09 /pmc/articles/PMC8453788/ /pubmed/33522595 http://dx.doi.org/10.1002/bit.27697 Text en © 2021 The Authors. Biotechnology and Bioengineering Published by Wiley Periodicals LLC https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle ARTICLES
Coffman, Jon
Bibbo, Kenneth
Brower, Mark
Forbes, Robert
Guros, Nicholas
Horowski, Brian
Lu, Rick
Mahajan, Rajiv
Patil, Ujwal
Rose, Steven
Shultz, Joseph
The design basis for the integrated and continuous biomanufacturing framework
title The design basis for the integrated and continuous biomanufacturing framework
title_full The design basis for the integrated and continuous biomanufacturing framework
title_fullStr The design basis for the integrated and continuous biomanufacturing framework
title_full_unstemmed The design basis for the integrated and continuous biomanufacturing framework
title_short The design basis for the integrated and continuous biomanufacturing framework
title_sort design basis for the integrated and continuous biomanufacturing framework
topic ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8453788/
https://www.ncbi.nlm.nih.gov/pubmed/33522595
http://dx.doi.org/10.1002/bit.27697
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