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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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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. |
format | Online Article Text |
id | pubmed-10608304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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