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Integration of a perfusion reactor and continuous precipitation in an entirely membrane‐based process for antibody capture

Continuous precipitation coupled with continuous tangential flow filtration is a cost‐effective alternative for the capture of recombinant antibodies from crude cell culture supernatant. The removal of surge tanks between unit operations, by the adoption of tubular reactors, maintains a continuous h...

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Autores principales: Recanati, Gabriele, Pappenreiter, Magdalena, Gstoettner, Christoph, Scheidl, Patrick, Vega, Elena Domínguez, Sissolak, Bernhard, Jungbauer, Alois
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10545976/
https://www.ncbi.nlm.nih.gov/pubmed/37795344
http://dx.doi.org/10.1002/elsc.202300219
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author Recanati, Gabriele
Pappenreiter, Magdalena
Gstoettner, Christoph
Scheidl, Patrick
Vega, Elena Domínguez
Sissolak, Bernhard
Jungbauer, Alois
author_facet Recanati, Gabriele
Pappenreiter, Magdalena
Gstoettner, Christoph
Scheidl, Patrick
Vega, Elena Domínguez
Sissolak, Bernhard
Jungbauer, Alois
author_sort Recanati, Gabriele
collection PubMed
description Continuous precipitation coupled with continuous tangential flow filtration is a cost‐effective alternative for the capture of recombinant antibodies from crude cell culture supernatant. The removal of surge tanks between unit operations, by the adoption of tubular reactors, maintains a continuous harvest and mass flow of product with the advantage of a narrow residence time distribution (RTD). We developed a continuous process implementing two orthogonal precipitation methods, CaCl(2) precipitation for removal of host‐cell DNA and polyethylene glycol (PEG) for capturing the recombinant antibody, with no influence on the glycosylation profile. Our lab‐scale prototype consisting of two tubular reactors and two stages of tangential flow microfiltration was continuously operated for up to 8 days in a truly continuous fashion and without any product flow interruption, both as a stand‐alone capture and as an integrated perfusion‐capture. Furthermore, we explored the use of a negatively charged membrane adsorber for flow‐through anion exchange as first polishing step. We obtained a product recovery of approximately 80% and constant product quality, with more than two logarithmic reduction values (LRVs) for both host‐cell proteins and host‐cell DNA by the combination of the precipitation‐based capture and the first polishing step.
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spelling pubmed-105459762023-10-04 Integration of a perfusion reactor and continuous precipitation in an entirely membrane‐based process for antibody capture Recanati, Gabriele Pappenreiter, Magdalena Gstoettner, Christoph Scheidl, Patrick Vega, Elena Domínguez Sissolak, Bernhard Jungbauer, Alois Eng Life Sci Research Articles Continuous precipitation coupled with continuous tangential flow filtration is a cost‐effective alternative for the capture of recombinant antibodies from crude cell culture supernatant. The removal of surge tanks between unit operations, by the adoption of tubular reactors, maintains a continuous harvest and mass flow of product with the advantage of a narrow residence time distribution (RTD). We developed a continuous process implementing two orthogonal precipitation methods, CaCl(2) precipitation for removal of host‐cell DNA and polyethylene glycol (PEG) for capturing the recombinant antibody, with no influence on the glycosylation profile. Our lab‐scale prototype consisting of two tubular reactors and two stages of tangential flow microfiltration was continuously operated for up to 8 days in a truly continuous fashion and without any product flow interruption, both as a stand‐alone capture and as an integrated perfusion‐capture. Furthermore, we explored the use of a negatively charged membrane adsorber for flow‐through anion exchange as first polishing step. We obtained a product recovery of approximately 80% and constant product quality, with more than two logarithmic reduction values (LRVs) for both host‐cell proteins and host‐cell DNA by the combination of the precipitation‐based capture and the first polishing step. John Wiley and Sons Inc. 2023-09-07 /pmc/articles/PMC10545976/ /pubmed/37795344 http://dx.doi.org/10.1002/elsc.202300219 Text en © 2023 The Authors. Engineering in Life Sciences published by Wiley‐VCH GmbH. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Recanati, Gabriele
Pappenreiter, Magdalena
Gstoettner, Christoph
Scheidl, Patrick
Vega, Elena Domínguez
Sissolak, Bernhard
Jungbauer, Alois
Integration of a perfusion reactor and continuous precipitation in an entirely membrane‐based process for antibody capture
title Integration of a perfusion reactor and continuous precipitation in an entirely membrane‐based process for antibody capture
title_full Integration of a perfusion reactor and continuous precipitation in an entirely membrane‐based process for antibody capture
title_fullStr Integration of a perfusion reactor and continuous precipitation in an entirely membrane‐based process for antibody capture
title_full_unstemmed Integration of a perfusion reactor and continuous precipitation in an entirely membrane‐based process for antibody capture
title_short Integration of a perfusion reactor and continuous precipitation in an entirely membrane‐based process for antibody capture
title_sort integration of a perfusion reactor and continuous precipitation in an entirely membrane‐based process for antibody capture
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10545976/
https://www.ncbi.nlm.nih.gov/pubmed/37795344
http://dx.doi.org/10.1002/elsc.202300219
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