Model based adaptive control of a continuous capture process for monoclonal antibodies production

•It is shown how a continuous capture process can be designed and operated in a continuous integrated process with optimal performance.•A novel two column capture process, capable of continuously processing a feed stream, is presented.•The process was designed using a novel mechanistic model for aff...

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Veröffentlicht in:Journal of Chromatography A 2016-04, Vol.1444, p.50-56
Hauptverfasser: Steinebach, Fabian, Angarita, Monica, Karst, Daniel J., Müller-Späth, Thomas, Morbidelli, Massimo
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container_end_page 56
container_issue
container_start_page 50
container_title Journal of Chromatography A
container_volume 1444
creator Steinebach, Fabian
Angarita, Monica
Karst, Daniel J.
Müller-Späth, Thomas
Morbidelli, Massimo
description •It is shown how a continuous capture process can be designed and operated in a continuous integrated process with optimal performance.•A novel two column capture process, capable of continuously processing a feed stream, is presented.•The process was designed using a novel mechanistic model for affinity capture.•Compared to two column continuous batch-wise capture, the countercurrent operation results in a much more economic process. A two-column capture process for continuous processing of cell-culture supernatant is presented. Similar to other multicolumn processes, this process uses sequential countercurrent loading of the target compound in order maximize resin utilization and productivity for a given product yield. The process was designed using a novel mechanistic model for affinity capture, which takes both specific adsorption as well as transport through the resin beads into account. Simulations as well as experimental results for the capture of an IgG antibody are discussed. The model was able to predict the process performance in terms of yield, productivity and capacity utilization. Compared to continuous capture with two columns operated batch wise in parallel, a 2.5-fold higher capacity utilization was obtained for the same productivity and yield. This results in an equal improvement in product concentration and reduction of buffer consumption. The developed model was used not only for the process design and optimization but also for its online control. In particular, the unit operating conditions are changed in order to maintain high product yield while optimizing the process performance in terms of capacity utilization and buffer consumption also in the presence of changing upstream conditions and resin aging.
doi_str_mv 10.1016/j.chroma.2016.03.014
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A two-column capture process for continuous processing of cell-culture supernatant is presented. Similar to other multicolumn processes, this process uses sequential countercurrent loading of the target compound in order maximize resin utilization and productivity for a given product yield. The process was designed using a novel mechanistic model for affinity capture, which takes both specific adsorption as well as transport through the resin beads into account. Simulations as well as experimental results for the capture of an IgG antibody are discussed. The model was able to predict the process performance in terms of yield, productivity and capacity utilization. Compared to continuous capture with two columns operated batch wise in parallel, a 2.5-fold higher capacity utilization was obtained for the same productivity and yield. This results in an equal improvement in product concentration and reduction of buffer consumption. 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subjects Adsorption
Antibodies, Monoclonal - isolation & purification
Antibody purification
Biotechnology - instrumentation
Biotechnology - methods
Buffers
Cell Culture Techniques
Consumption
Continuous bioprocessing
Continuous chromatography
Countercurrent Distribution
Immunoglobulin G - isolation & purification
Mathematical models
Models, Biological
Optimization
Polymers
Process control
Productivity
Protein A affinity chromatography
Resins
Resins, Synthetic - chemistry
Utilization
title Model based adaptive control of a continuous capture process for monoclonal antibodies production
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