Evidence map›Paper›PMID 40443054›Full record

ArticleBiotechnology and bioengineering2025

Techno-Economic Analysis of Membrane-Based Purification Platforms for AAV Vector Production.

Juan J Romero, Eleanor W Jenkins, Jacob I Monroe, S Ranil Wickramasinghe, Xianghong Qian, Dibakar Bhattacharyya, Scott M Husson

Abstract 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. 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

7 authors.

Juan J RomeroDepartment of Chemical and Biomolecular Engineering, Clemson University, Clemson, South Carolina, USA.
Eleanor W JenkinsSchool of Mathematical and Statistical Sciences, Clemson University, Clemson, South Carolina, USA.
Jacob I MonroeRalph E. Martin Department of Chemical Engineering, University of Arkansas, Fayetteville, Arkansas, USA.
S Ranil WickramasingheRalph E. Martin Department of Chemical Engineering, University of Arkansas, Fayetteville, Arkansas, USA.
Xianghong QianDepartment of Biomedical Engineering, University of Arkansas, Fayetteville, Arkansas, USA.ORCID https://orcid.org/0000-0001-5619-9782
Dibakar BhattacharyyaDepartment of Chemical and Materials Engineering, University of Kentucky, Lexington, Kentucky, USA.
Scott M HussonDepartment of Chemical and Biomolecular Engineering, Clemson University, Clemson, South Carolina, USA.ORCID https://orcid.org/0000-0002-8830-8530

Funding

This study was funded by the National Science Foundation under awards EPSCoR Track 2 (RII 2218054), OIA-2218054 and DMS-2011902.
6 · The paper itself

Abstract

Technologies for large-scale manufacturing of viral vectors for gene therapies, such as tangential flow filtration and membrane chromatography, are under development. In these early stages of process development, techno-economic analyses are useful for identifying membrane properties yielding the greatest impact on process performance. In this study, we adapted a techno-economic framework used for monoclonal antibody capture for adeno-associated viral vector purification. We added mechanistic models to simulate flux decline during harvesting and separating full and empty capsids during polishing. Graphical user interfaces were added to help users explore the design search space. We selected a base process and manipulated selected variables to see their impact on large-scale manufacturing performance. These sensitivity analyses revealed that, under the selected process conditions, increasing module capacity reduces cost of goods more effectively than increasing operational flux in tangential flow membrane filtration modules for virus harvesting. Membrane chromatography columns with relatively low dynamic binding capacity (DBC) and short residence time (RT) offered similar or better economic performance than those with high DBC and long RT. Additionally, the difference in equilibrium solid-phase concentration between full and empty capsids as a function of salt concentration significantly affects purity.

Indexed as

BiotechnologyDependovirusFiltrationGenetic VectorsChromatographyMembranes, ArtificialMembranes, Artificialbioprocess cost modelsmembrane designmodel‐based simulationvector‐based gene therapy

Identifiers

PMID40443054
PMCPMC12322620

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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.