Raman‐controlled pyruvate feeding to control metabolic activity and product quality in continuous biomanufacturing

Author:

Romann Patrick12ORCID,Schneider Sebastian1,Tobler Daniela1,Jordan Martin3,Perilleux Arnaud3,Souquet Jonathan3,Herwig Christoph2ORCID,Bielser Jean‐Marc3,Villiger Thomas K.1ORCID

Affiliation:

1. Institute for Pharma Technology School of Life Science University of Applied Sciences and Arts Northwestern Switzerland Muttenz Switzerland

2. Research Division Biochemical Engineering Institute of Chemical Environmental and Bioscience Engineering Vienna University of Technology Vienna Austria

3. Biotech Process Science Merck Serono SA (an affiliate of Merck KGaA, Darmstadt, Germany) Corsier‐sur‐Vevey Switzerland

Abstract

AbstractBackgroundDespite technological advances ensuring stable cell culture perfusion operation over prolonged time, reaching a cellular steady‐state metabolism remains a challenge for certain manufacturing cell lines. This study investigated the stabilization of a steady‐state perfusion process producing a bispecific antibody with drifting product quality attributes, caused by shifting metabolic activity in the cell culture.Main methodsA novel on‐demand pyruvate feeding strategy was developed, leveraging lactate as an indicator for tricarboxylic acid (TCA) cycle saturation. Real‐time lactate monitoring was achieved through in‐line Raman spectroscopy, enabling accurate control at predefined target setpoints.Major resultsThe implemented feedback control strategy resulted in a three‐fold reduction of ammonium accumulation and stabilized product quality profiles. Stable and flat glycosylation profiles were achieved with standard deviations below 0.2% for high mannose and fucosylation. Whereas galactosylation and sialylation were stabilized in a similar manner, varying lactate setpoints might allow for fine‐tuning of these glycan forms.ImplicationThe Raman‐controlled pyruvate feeding strategy represents a valuable tool for continuous manufacturing, stabilizing metabolic activity, and preventing product quality drifting in perfusion cell cultures. Additionally, this approach effectively reduced high mannose, helping to mitigate increases associated with process intensification, such as extended culture durations or elevated culture densities.

Publisher

Wiley

Subject

Molecular Medicine,Applied Microbiology and Biotechnology,General Medicine

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