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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

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

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.

Original languageEnglish
Pages (from-to)2400-2409
Number of pages10
JournalBiotechnology and Bioengineering
Volume122
Issue number9
DOIs
StatePublished - Sep 2025

Bibliographical note

Publisher Copyright:
© 2025 The Author(s). Biotechnology and Bioengineering published by Wiley Periodicals LLC.

Funding

S.M.H. acknowledges support from the William B. “Bill” Sturgis, ‘57 and Martha Elizabeth “Martha Beth” Blackmon Sturgis Distinguished Professorship in Chemical and Biomolecular Engineering. This study was funded by the National Science Foundation under awards EPSCoR Track 2 (RII 2218054), OIA‐2218054 and DMS‐2011902 is gratefully acknowledged.

FundersFunder number
National Science Foundation Arctic Social Science ProgramOIA‐2218054, RII 2218054, DMS‐2011902

    Keywords

    • bioprocess cost models
    • membrane design
    • model-based simulation
    • vector-based gene therapy

    ASJC Scopus subject areas

    • Biotechnology
    • Bioengineering
    • Applied Microbiology and Biotechnology

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