Evidence map›Paper›PMID 42272436›Full record

ArticlemAbs2026

NMR detects clustering and ultra-weak excipient interactions governing monoclonal antibody viscosity in formulation-relevant conditions.

Liza Boëffard-Dosierre, Camille Dagallier, Géraldine Eudier, Vasco Filipe, Atifa Badar-Majeed, Solène Fraumont, Sophie Zinn-Justin, Francois-Xavier Theillet

Abstract read
In one paragraph

Article in mAbs, 2026. 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

8 authors.

Liza Boëffard-DosierreInstitute for Integrative Biology of the Cell (I2BC), Université Paris-Saclay, CEA, CNRS, Gif-sur-Yvette, France.ORCID 0009-0009-5935-961X
Camille DagallierSanofi R&D, Biologics Drug Products Development & Manufacturing, Vitry-Sur-Seine, France.ORCID 0000-0002-6757-3570
Géraldine EudierSanofi R&D, Biologics Drug Products Development & Manufacturing, Vitry-Sur-Seine, France.ORCID 0009-0007-2693-0758
Vasco FilipeSanofi R&D, Biologics Drug Products Development & Manufacturing, Vitry-Sur-Seine, France.ORCID 0009-0008-0272-8181
Atifa Badar-MajeedInstitute for Integrative Biology of the Cell (I2BC), Université Paris-Saclay, CEA, CNRS, Gif-sur-Yvette, France.
Solène FraumontInstitute for Integrative Biology of the Cell (I2BC), Université Paris-Saclay, CEA, CNRS, Gif-sur-Yvette, France.
Sophie Zinn-JustinInstitute for Integrative Biology of the Cell (I2BC), Université Paris-Saclay, CEA, CNRS, Gif-sur-Yvette, France.ORCID 0000-0002-7680-1088
Francois-Xavier TheilletInstitute for Integrative Biology of the Cell (I2BC), Université Paris-Saclay, CEA, CNRS, Gif-sur-Yvette, France.ORCID 0000-0002-3264-210X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

High-concentration formulations of monoclonal antibodies (mAbs) are required for subcutaneous administration but are frequently challenging to develop due to elevated viscosity and colloidal instability. These properties are governed by mAb-mAb interactions that are regulated by additional mAb-excipient interactions. These ultra-weak interactions remain difficult to characterize using conventional techniques. Here, we combined nuclear magnetic resonance (NMR) spectroscopy with rheometry and dynamic light scattering to investigate mAb interactions under formulation-relevant conditions. Rheological measurements showed that, in the case of the chosen mAb, the excipients arginine and lysine strongly reduce the macroscopic viscosity, whereas other excipients display a moderate effect by themselves. Characterization of the mAb oligomeric state by

Indexed as

Antibodies, MonoclonalExcipientsMagnetic Resonance SpectroscopyViscosityAntibodies, MonoclonalExcipientsExcipientsformulation developmentmonoclonal antibodiesNMR spectroscopyprotein–excipient interactionsviscosity

Identifiers

PMID42272436
PMCPMC13271275

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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.