Evidence map›Paper›PMID 42509331›Full record

ArticleNature materials2026

Force-responsive biomaterials drive tissue repair by harnessing endogenous growth factors.

Magdalene Y Ho, Nuria Oliva, Christopher Basu, Marcos R Rodriguez, Jose Antonio Duran-Mota, Divya M Gollapalli, Victor G Szwarcberg, Mo Akhavani, Kyle P Quinn, Benjamin D Almquist

Abstract read
In one paragraph

Article in Nature materials, 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

10 authors.

Magdalene Y HoDepartment of Bioengineering, Imperial College London, London, UK.ORCID 0000-0001-7700-0293
Nuria OlivaDepartment of Bioengineering, Imperial College London, London, UK.ORCID 0000-0002-6305-0801
Christopher BasuDepartment of Bioengineering, Imperial College London, London, UK.
Marcos R RodriguezDepartment of Biomedical Engineering, University of Arkansas, Fayetteville, AR, USA.ORCID 0000-0003-2883-3971
Jose Antonio Duran-MotaDepartment of Bioengineering, Imperial College London, London, UK.ORCID 0000-0003-1864-5248
Divya M GollapalliDepartment of Biomedical Engineering, University of Arkansas, Fayetteville, AR, USA.ORCID 0009-0004-3767-9202
Victor G SzwarcbergDepartment of Bioengineering, Imperial College London, London, UK.ORCID 0009-0003-1027-1269
Mo AkhavaniDepartment of Plastic and Reconstructive Surgery, Royal Free Hospital, London, UK.
Kyle P QuinnDepartment of Biomedical Engineering, University of Arkansas, Fayetteville, AR, USA.ORCID 0000-0002-6876-3608
Benjamin D AlmquistDepartment of Bioengineering, Imperial College London, London, UK. b.almquist@imperial.ac.uk.ORCID 0000-0001-9718-777X

Funding

Unraveling Gene-Environment Interactions Shaping Metabolism: A Multi-Omics Analysis in DrosophilaP20GM139768 · NIGMS · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI Joanna Fiddler · 2021 to 2026
$17.0M
Non-invasive automated wound analysis via deep learning neural networksR01EB031032 · NIBIB · UNIVERSITY OF ARKANSAS AT FAYETTEVILLE · PI QUINN, KYLE PATRICK · 2021 to 2024
$1.6M
NIBIB NIH HHS R01 EB031032NIGMS NIH HHS P20 GM139768RCUK | Biotechnology and Biological Sciences Research Council (BBSRC) BB/T017929/1RCUK | Medical Research Council (MRC) MR/X502959/1
6 · The paper itself

Abstract

Materials enabling the cell-responsive delivery of endogenous biologics, such as growth factors, have the potential to modulate wound repair cost-effectively and safely. Unlike passive drug delivery strategies that require supraphysiological doses of recombinant protein or stimuli-responsive systems that rely on external triggers, we demonstrate a strategy that harnesses cellular traction forces as an intrinsic delivery trigger. Traction-force-activated payloads are bioinspired aptamer constructs attached to biomaterial scaffolds that selectively harvest, concentrate and reactivate multiple endogenous growth factors from cells, injury sites and blood lysate in vivo (rat femur and mouse skin) and ex vivo (human skin), at doses orders of magnitude lower than current clinical standards. Unmodified oligonucleotide aptamers retain functionality in enzyme-rich wound environments, substantially expanding the translational potential of nucleic-acid-based therapeutics. The ability to harvest and redeliver endogenous growth factors without exogenous triggers, recombinant proteins or cold-chain logistics via mechanoresponsive biomaterials opens possibilities for accessible, cost-effective combinatorial biologic therapies.

Indexed as

Biocompatible MaterialsIntercellular Signaling Peptides and ProteinsWound HealingAnimalsAptamers, NucleotideHumansMiceRatsAptamers, NucleotideBiocompatible MaterialsIntercellular Signaling Peptides and Proteins

Identifiers

PMID42509331
PMCPMC13518237

What OpenQuestion holds

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Registered trials

None linked

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.