Evidence map›Paper›PMID 41868385›Full record

ReviewNanoscale advances2026

Massart iron oxide nanoparticles in mechanobiology.

Myriam Reffay, Gilles Tessier, Jean-François Berret

Abstract readReview
In one paragraph

Review in Nanoscale advances, 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

3 authors.

Myriam ReffayUniversité Paris Cité, CNRS, Matière et Systèmes Complexes 75013 Paris France jean-francois.berret@u-paris.fr.ORCID https://orcid.org/0000-0002-3695-2789
Gilles TessierSorbonne Université, INSERM, CNRS, Institut de la Vision 17 rue Moreau F-75012, Paris France.ORCID https://orcid.org/0000-0003-3558-925X
Jean-François BerretUniversité Paris Cité, CNRS, Matière et Systèmes Complexes 75013 Paris France jean-francois.berret@u-paris.fr.ORCID https://orcid.org/0000-0001-5458-8653

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Magnetic nanoparticles (MNPs) derived from the Massart coprecipitation method have played a pioneering role in bridging materials science and biology. Their magnetic moment and nanoscale dimensions have long enabled applications in magnetic resonance imaging, targeted drug delivery, separation technologies, and hyperthermia. Beyond these well-established uses, a growing research direction has emerged at the interface of physics and biology: the application of MNPs in mechanobiology, the study of how mechanical forces regulate cellular and tissue functions. This review examines how Massart MNPs can be used to generate, transmit, and measure forces within living systems. Particular attention is given to interfacial control through advanced surface chemistries, which ensure colloidal stability, minimize toxicity, and preserve the nanoscale integrity of the particles. We also show that the robustness and scalability of Massart synthesis make it ideally suited to the production of biocompatible nanomaterials in quantities required for comprehensive biological studies. Two complementary approaches are discussed. The first exploits MNP assemblies that arise spontaneously within cells, in the form of endosomes. These compartments enable the application of controlled magnetic forces to study both the formation of reconstructed tissues and organoids, and their viscoelastic response. The second focuses on micrometric magnetic wires fabricated from MNPs, used in active microrheology to probe the cytoplasm of living cells over a wide frequency range. Together, these approaches illustrate how MNP assemblies can accurately quantify cellular and tissue mechanics, providing new opportunities for mechanobiological studies and enabling the development of novel readouts of cellular mechanics with potential diagnostic applications.

Identifiers

PMID41868385
PMCPMC13000760

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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.