Evidence map›Paper›PMID 42415185›Full record

ArticleBiotechnology progress

Application of commercial ultrafiltration membranes for protein purification by high performance countercurrent membrane purification (HPCMP).

Aylin Mohammadzadehmarandi, Nate Heller, Mohammadreza Ahmadimashhadi, Jon Petrone, Nicholas Marchand, Siavash Darvishmanesh, Ka Zhang, Stefano Menegatti, Andrew L Zydney

Abstract read
In one paragraph

Article in Biotechnology progress. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Aylin MohammadzadehmarandiDepartment of Chemical Engineering, The Pennsylvania State University, University Park, Pennsylvania, USA.
Nate HellerDepartment of Chemical Engineering, The Pennsylvania State University, University Park, Pennsylvania, USA.
Mohammadreza AhmadimashhadiDepartment of Biomedical Engineering, The Pennsylvania State University, University Park, Pennsylvania, USA.
Jon PetroneCytiva, Marlborough, Massachusetts, USA.
Nicholas MarchandCytiva, Marlborough, Massachusetts, USA.
Siavash DarvishmaneshCytiva, Marlborough, Massachusetts, USA.
Ka ZhangDepartment of Chemical Engineering, The North Carolina State University, Raleigh, North Carolina, USA.
Stefano MenegattiDepartment of Chemical Engineering, The North Carolina State University, Raleigh, North Carolina, USA.
Andrew L ZydneyDepartment of Chemical Engineering, The Pennsylvania State University, University Park, Pennsylvania, USA.ORCID https://orcid.org/0000-0003-1865-9156

Funding

National Science Foundation 1841474National Science Foundation 2310832
6 · The paper itself

Abstract

High performance countercurrent membrane purification (HPCMP) has emerged as a promising diffusive separation strategy for the purification of recombinant proteins and monoclonal antibodies (mAbs). However, prior studies employed dialysis membranes, which are designed for diffusive separations but have not been validated for biopharmaceutical manufacturing. This study evaluates the ability of commercial ultrafiltration (UF) membranes, engineered for pressure-driven filtration, to support highly selective diffusive separations. Scanning electron microscopy (SEM) analysis of the membrane cross-sections revealed marked morphological differences between UF and dialysis membranes. Yet, transport studies using polydisperse dextrans and model proteins demonstrated that UF membranes can deliver exceptional diffusive separation selectivity. In particular, a 100 kDa polysulfone membrane (Cytiva) provided >150-fold diffusive selectivity between bovine serum albumin (BSA) and immunoglobulin G (IgG). When utilized for mAb separation from a clarified CHO cell culture fluid, this membrane achieved >98% product yield, near-complete removal of low molecular weight species, and significant reduction in both DNA and host cell protein (HCP) levels. These results demonstrate that commercial UF membranes that are validated for bioprocessing applications can be repurposed for HPCMP, enabling scalable, continuous downstream processing of biotherapeutics.

Indexed as

Antibodies, MonoclonalMembranes, ArtificialRecombinant ProteinsAnimalsCattleCHO CellsCountercurrent DistributionCricetinaeCricetulusImmunoglobulin GSerum Albumin, BovineUltrafiltrationAntibodies, MonoclonalImmunoglobulin GMembranes, ArtificialRecombinant ProteinsSerum Albumin, Bovinebioprocessingbioseparationsdiffusive transportmembranesmonoclonal antibody

Identifiers

PMID42415185
PMCPMC13636633

What OpenQuestion holds

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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.