Evidence map›Paper›PMID 39558516›Full record

ArticleBiotechnology and bioengineering2025

Regeneration of Spent Culture Media for Sustainable and Continuous mAb Production via Ion Concentration Polarization.

Eric Wynne, Junghyo Yoon, Dohyun Park, Mingyang Cui, Caitlin Morris, Jaeweon Lee, Zhao Wang, Seongkyu Yoon, Jongyoon Han

Erratum issuedAbstract read
In one paragraph

Article in Biotechnology and bioengineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Eric WynneDepartment of Electrical Engineering and Computer Science, College of Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.ORCID 0000-0002-4866-5066
Junghyo YoonResearch Laboratory of Electronics, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Dohyun ParkResearch Laboratory of Electronics, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Mingyang CuiResearch Laboratory of Electronics, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.
Caitlin MorrisDepartment of Chemical Engineering, University of Massachusetts Lowell, Lowell, Massachusetts, USA.
Jaeweon LeeDepartment of Chemical Engineering, University of Massachusetts Lowell, Lowell, Massachusetts, USA.ORCID 0000-0002-2067-3857
Zhao WangDepartment of Chemical Engineering, University of Massachusetts Lowell, Lowell, Massachusetts, USA.
Seongkyu YoonDepartment of Chemical Engineering, University of Massachusetts Lowell, Lowell, Massachusetts, USA.ORCID 0000-0002-5330-8784
Jongyoon HanDepartment of Electrical Engineering and Computer Science, College of Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts, USA.

Funding

This research was supported by the National Institute for Innovation in Manufacturing Biopharmaceuticals.
6 · The paper itself

Abstract

In modern bioprocessing, cell culture media is one of the most significant cost drivers, yet the nutrients and other critical factors in the media are often not fully utilized. With the renewed emphasis on reducing the cost of bioprocessing, there is much interest in reducing the overall use of cell culture media. In this work, we introduce a mesoscale microfluidic separation device based on the ion concentration polarization (ICP) process to regenerate the spent media for reuse by removing critical waste products from the cell culture that are known to inhibit the growth of the cells. We demonstrated that up to 75% of spent culture media can be regenerated and reused without affecting the cell viability. A detailed analysis of the materials consumed during antibody production indicated that one could improve the water process mass intensity by up to 33% by regenerating and recycling the media. Given that ICP separation systems have already been scaled up to support large-volume processing, it would be feasible to deploy this technology for manufacturing scale bioreactors (e.g., 50 L perfusion culture of CHO cells), reducing the overall operation cost and water use.

Indexed as

Antibodies, MonoclonalCell Culture TechniquesCricetulusCulture MediaAnimalsBioreactorsCell SurvivalCHO CellsCricetinaeAntibodies, MonoclonalCulture MediabiomanufacturingCHOion concentration polarizationsustainabilitywater conservation

Identifiers

PMID39558516
PMCPMC11718426

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.