Evidence map›Paper›PMID 42605573›Full record

ArticleBiotechnology journal2026

Anion-Exchange Membrane Chromatography for the Separation of Empty and Full Adeno-Associated Viral Capsids.

Luca Ossi, Samuele Delfino, Helena Marie, Michael Schulte, Mattia Sponchioni

Abstract read
In one paragraph

Article in Biotechnology journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

5 authors.

Luca OssiDepartment of Chemistry, Materials and Chemical Engineering, Politecnico Di Milano, Milano, Italy.
Samuele DelfinoDepartment of Chemistry, Materials and Chemical Engineering, Politecnico Di Milano, Milano, Italy.
Helena MarieMerck Life Science KGaA, Darmstad, Germany.
Michael SchulteMerck Life Science KGaA, Darmstad, Germany.
Mattia SponchioniDepartment of Chemistry, Materials and Chemical Engineering, Politecnico Di Milano, Milano, Italy.ORCID https://orcid.org/0000-0002-8130-6495

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The separation of empty and full adeno-associated viruses (AAVs) is particularly critical because of the similarity between the two. Anion-exchange chromatography represents a scalable tool, leveraging their slight difference in isoelectric point. However, traditional resin chromatography can only deliver poor resolution, mainly due to the restricted accessibility of the capisds to the bead pores. To cover this gap, in this work, we designed and optimized the separation of empty and full AAVs using anion-exchange membrane chromatography. The role played by flowrate, gradient slope and wash step parameters on the chromatographic resolution was first investigated with two consecutive designs of experiments (DoE). The response surfaces indicated that high process flowrates, that is 15 membrane volumes (MVs)/min, with a gradient from 115 mM to 250 mM sodium acetate in 350 MVs maximize the chromatographic resolution. Then, preparative experiments showed that fast loading is possible, with residence time as short as 24 s, without product breakthrough. Moreover, membrane loading up to 1.2E17 viral particles (vp)/L

Indexed as

CapsidDependovirusAnion Exchange ResinsChromatography, Ion ExchangeMembranes, ArtificialAnion Exchange ResinsMembranes, Artificialadeno‐associated virusesanion exchangedesign of experimentselution chromatographyempty/full separationmembrane chromatographyprocess optimization

Identifiers

PMID42605573
PMCPMC13478881

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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.