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Scalability of Sartobind(®) Rapid A Membrane for High Productivity Monoclonal Antibody Capture

Improved upstream titres in therapeutic monoclonal antibody (mAb) production have shifted capacity constraints to the downstream process. The consideration of membrane-based chromatographic devices as a debottlenecking option is gaining increasing attention with the recent introduction of high-capac...

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Autores principales: Yang, Sabrina, Braczkowski, Ryszard, Chen, Shih-Hsun, Busse, Ricarda, Li, Yudhi, Fabri, Louis, Bekard, Innocent Berbelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10608304/
https://www.ncbi.nlm.nih.gov/pubmed/37887987
http://dx.doi.org/10.3390/membranes13100815
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author Yang, Sabrina
Braczkowski, Ryszard
Chen, Shih-Hsun
Busse, Ricarda
Li, Yudhi
Fabri, Louis
Bekard, Innocent Berbelle
author_facet Yang, Sabrina
Braczkowski, Ryszard
Chen, Shih-Hsun
Busse, Ricarda
Li, Yudhi
Fabri, Louis
Bekard, Innocent Berbelle
author_sort Yang, Sabrina
collection PubMed
description Improved upstream titres in therapeutic monoclonal antibody (mAb) production have shifted capacity constraints to the downstream process. The consideration of membrane-based chromatographic devices as a debottlenecking option is gaining increasing attention with the recent introduction of high-capacity bind and elute membranes. We have evaluated the performance and scalability of the Sartobind(®) Rapid A affinity membrane (1 mL) for high-productivity mAb capture. For scalability assessment, a 75 mL prototype device was used to process 100 L of clarified cell culture harvest (CH) on a novel multi-use rapid cycling chromatography system (MU-RCC). MabSelect™ PrismA (4.7 mL) was used as a benchmark comparator for Protein A (ProtA) resin studies. Results show that in addition to a productivity gain of >10×, process and product quality attributes were either improved or comparable to the benchmark. Concentrations of eluate pools were 7.5× less than that of the benchmark, with the comparatively higher bulk volume likely to cause handling challenges at process scale. The MU-RCC system is capable of membrane operation at pilot scale with comparable product quality profile to the 1 mL device. The Sartobind(®) Rapid A membrane is a scalable alternative to conventional ProtA resin chromatography for the isolation and purification of mAbs from harvested cell culture media.
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spelling pubmed-106083042023-10-28 Scalability of Sartobind(®) Rapid A Membrane for High Productivity Monoclonal Antibody Capture Yang, Sabrina Braczkowski, Ryszard Chen, Shih-Hsun Busse, Ricarda Li, Yudhi Fabri, Louis Bekard, Innocent Berbelle Membranes (Basel) Article Improved upstream titres in therapeutic monoclonal antibody (mAb) production have shifted capacity constraints to the downstream process. The consideration of membrane-based chromatographic devices as a debottlenecking option is gaining increasing attention with the recent introduction of high-capacity bind and elute membranes. We have evaluated the performance and scalability of the Sartobind(®) Rapid A affinity membrane (1 mL) for high-productivity mAb capture. For scalability assessment, a 75 mL prototype device was used to process 100 L of clarified cell culture harvest (CH) on a novel multi-use rapid cycling chromatography system (MU-RCC). MabSelect™ PrismA (4.7 mL) was used as a benchmark comparator for Protein A (ProtA) resin studies. Results show that in addition to a productivity gain of >10×, process and product quality attributes were either improved or comparable to the benchmark. Concentrations of eluate pools were 7.5× less than that of the benchmark, with the comparatively higher bulk volume likely to cause handling challenges at process scale. The MU-RCC system is capable of membrane operation at pilot scale with comparable product quality profile to the 1 mL device. The Sartobind(®) Rapid A membrane is a scalable alternative to conventional ProtA resin chromatography for the isolation and purification of mAbs from harvested cell culture media. MDPI 2023-09-27 /pmc/articles/PMC10608304/ /pubmed/37887987 http://dx.doi.org/10.3390/membranes13100815 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Yang, Sabrina
Braczkowski, Ryszard
Chen, Shih-Hsun
Busse, Ricarda
Li, Yudhi
Fabri, Louis
Bekard, Innocent Berbelle
Scalability of Sartobind(®) Rapid A Membrane for High Productivity Monoclonal Antibody Capture
title Scalability of Sartobind(®) Rapid A Membrane for High Productivity Monoclonal Antibody Capture
title_full Scalability of Sartobind(®) Rapid A Membrane for High Productivity Monoclonal Antibody Capture
title_fullStr Scalability of Sartobind(®) Rapid A Membrane for High Productivity Monoclonal Antibody Capture
title_full_unstemmed Scalability of Sartobind(®) Rapid A Membrane for High Productivity Monoclonal Antibody Capture
title_short Scalability of Sartobind(®) Rapid A Membrane for High Productivity Monoclonal Antibody Capture
title_sort scalability of sartobind(®) rapid a membrane for high productivity monoclonal antibody capture
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10608304/
https://www.ncbi.nlm.nih.gov/pubmed/37887987
http://dx.doi.org/10.3390/membranes13100815
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