PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
March 23, 2026Biotechnology and Bioengineering2 citations

Pseudo Perfusion of Chinese Hamster Ovary (CHO) Cells as a Reliable Platform for Data Generation to Model and Guide Continuous Perfusion Biomanufacturing

View Full Paper
NMNikola G. MalinovSBShivam BarodiyaMIMarianthi Ierapetritou

Key Points

  • This research aims to validate a pseudo perfusion platform for enhancing monoclonal antibody production in continuous biomanufacturing.
  • Developed a phenotype-driven pseudo perfusion platform
  • Validated the platform's ability to emulate continuous perfusion characteristics
  • Characterized metabolic data and cell parameters during the process
  • The pseudo perfusion platform improves predictions of amino acid demands in bioreactors
  • Demonstrated exceptional correlation across various cell-specific perfusion rates
  • Increased the reliability and dimensionality of metabolic datasets for process development

Abstract

ABSTRACT Chinese Hamster Ovary (CHO) cell monoclonal antibody (mAb) production in continuous perfusion has witnessed a renewed interest within the biopharmaceutical industry. Widespread implementation of perfusion biomanufacturing, however, remains hindered by long process development timelines and high costs. Use of predictive scale‐down platforms to generate large informative metabolic datasets and guide process development decisions is critical to decreasing a molecule's time to market. While scale‐down platforms based on the pseudo perfusion concept have been previously reported, they have not been rigorously validated. They are often limited by oxygen transport or insufficient metabolic characterization, reducing their role to a preliminary screening tool. Here, we report the design and validation of a pseudo perfusion platform based on a phenotype‐driven approach to ascertain that the process emulates continuous perfusion characteristics and is not oxygen limited. Beyond metabolic and cell size steady state, we show that our pseudo perfusion design enables cell cycle subpopulation and intracellular antibody expression steady state. We also demonstrate that pseudo perfusion robustly predicts amino acid demands in continuous perfusion bioreactors with exceptional linear correlation across a broad range of cell‐specific perfusion rates. When coupling the pseudo perfusion platform developed here with a workflow for metabolic characterization, we significantly augment the dimensionality and reliability of data which can be generated at this scale to gain actionable insights towards perfusion process design, ultimately reducing process development timelines and the associated costs.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Malinov et al. (2026) studied this question.

synapsesocial.com/papers/69c08b6ba48f6b84677f8a8ahttps://doi.org/10.1002/bit.70190
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Hybrid modeling for in silico optimization of a dynamic perfusion cell culture process2024 · 3 citations
  2. 2Multi-strategy nonlinear model predictive control for Chinese hamster ovary continuous process2026
  3. 3Two scale‐down tools for the optimization of perfusion bioreactors for the manufacture of biopharmaceuticals2024
  4. 4Cell specific perfusion rates drive growth dynamics and metabolism in CHO N-1 perfusion processes independent of perfusion rate control method2025
  5. 5Enhancing <scp>CHO</scp> cell recombinant protein production using a perfusion‐directed host evolution approach2025