Process analytical technique (PAT) miniaturization for monoclonal antibody aggregate detection in continuous downstream processing

The transition to continuous biomanufacturing is considered the next step to reduce costs and improve process robustness in the biopharmaceutical industry, while also improving productivity and product quality. The platform production process for monoclonal antibodies (mAbs) is eligible for continuo...

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Veröffentlicht in:Journal of chemical technology and biotechnology (1986) 2022-09, Vol.97 (9), p.2347-2364
Hauptverfasser: São Pedro, Mariana N, Klijn, Marieke E, Eppink, Michel HM, Ottens, Marcel
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container_issue 9
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container_title Journal of chemical technology and biotechnology (1986)
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creator São Pedro, Mariana N
Klijn, Marieke E
Eppink, Michel HM
Ottens, Marcel
description The transition to continuous biomanufacturing is considered the next step to reduce costs and improve process robustness in the biopharmaceutical industry, while also improving productivity and product quality. The platform production process for monoclonal antibodies (mAbs) is eligible for continuous processing to lower manufacturing costs due to patent expiration and subsequent growing competition. One of the critical quality attributes of interest during mAb purification is aggregate formation, with several processing parameters and environmental factors known to influence antibody aggregation. Therefore, a real‐time measurement to monitor aggregate formation is crucial to have immediate feedback and process control and to achieve a continuous downstream processing. Miniaturized biosensors as an in‐line process analytical technology tool could play a pivotal role to facilitate the transition to continuous manufacturing. In this review, miniaturization of already well‐established methods to detect protein aggregation, such as dynamic light scattering, Raman spectroscopy and circular dichroism, will be extensively evaluated for the possibility of providing a real‐time measurement of mAb aggregation. The method evaluation presented in this review shows which limitations of each analytical method still need to be addressed and provides application examples of each technique for mAb aggregate characterization. Additionally, challenges related to miniaturization are also addressed, such as the design of the microfluidic chip and the microfabrication material. The evaluation provided in this review shows why the development of microfluidic biosensors is considered the key for real‐time measurement of mAb aggregates and how it can contribute to the transition to a continuous processing. © 2021 The Authors. Journal of Chemical Technology and Biotechnology published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry (SCI).
doi_str_mv 10.1002/jctb.6920
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subjects Agglomeration
Biopharmaceuticals
Biosensors
Biotechnology
Chemical technology
Circular dichroism
continuous biomanufacturing
Dichroism
Environmental factors
Evaluation
Light scattering
Mathematical analysis
Microfluidics
Miniaturization
Monoclonal antibodies
Photon correlation spectroscopy
process analytical technology (PAT)
Process control
Process controls
Process parameters
Production costs
protein aggregation
Protein interaction
Quality management
Raman spectroscopy
Reviews
Technology assessment
Time measurement
title Process analytical technique (PAT) miniaturization for monoclonal antibody aggregate detection in continuous downstream processing
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