Evidence map›Paper›PMID 41744561›Full record

ArticleBiomimetics (Basel, Switzerland)2026

Natural Nacre-Derived Biomimetic Materials for In Vivo Bone Regeneration.

Pierre-Yves Collart-Dutilleul, Naveen Fatima, Richard Younes, Frédéric Cuisinier, Véronique Barragan-Montero, Alban Desoutter

Abstract read
In one paragraph

Article in Biomimetics (Basel, Switzerland), 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

6 authors.

Pierre-Yves Collart-DutilleulLaboratory Bioengineering Nanosciences (LBN), University of Montpellier, 34193 Montpellier, France.ORCID 0000-0003-3017-6843
Naveen FatimaLaboratory Bioengineering Nanosciences (LBN), University of Montpellier, 34193 Montpellier, France.
Richard YounesLaboratory Bioengineering Nanosciences (LBN), University of Montpellier, 34193 Montpellier, France.
Frédéric CuisinierLaboratory Bioengineering Nanosciences (LBN), University of Montpellier, 34193 Montpellier, France.ORCID 0000-0001-6870-0490
Véronique Barragan-MonteroLaboratory Bioengineering Nanosciences (LBN), University of Montpellier, 34193 Montpellier, France.ORCID 0000-0002-3397-9265
Alban DesoutterLaboratory Bioengineering Nanosciences (LBN), University of Montpellier, 34193 Montpellier, France.ORCID 0000-0001-9302-3890

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone regeneration in critical-size defects requires biomaterials that provide both structural support and appropriate osteoinductive cues. Natural nacre contains an organic matrix rich in acidic macromolecules with reported osteogenic activity; however, its in vivo regenerative potential remains insufficiently explored. This study evaluated the bone regenerative capacity of nacre-derived materials alone and combined with oxidized porous silicon microparticles (pSi-MP), a bioactive material known to release silicic acid and support mineralized tissue formation. Critical-size defects were created in four caudal vertebrae of Wistar rats and filled with nacre, pSi-MP, a nacre-pSi composite, or left empty. After 60 days, bone formation was assessed using micro-computed tomography and non-decalcified histology. Empty defects failed to regenerate, whereas nacre and pSi-MP individually promoted partial mineralized tissue deposition. The nacre-pSi composite produced the most extensive repair, showing near-complete defect bridging, higher bone mineral density, and seamless integration of particles within newly formed bone. No inflammation or adverse reactions were observed, and osteoid deposition occurred directly on material surfaces. These findings demonstrate that nacre-derived materials exert intrinsic osteogenic effects in vivo and that combining nacre with porous silicon yields a synergistic response that significantly enhances bone regeneration. The composite represents a promising candidate for future bone repair strategies.

Indexed as

biomimetic materialsbone regenerationcritical-size defectnacre proteinsosteoinductionporous silicon microparticlestissue engineering

Identifiers

PMID41744561
PMCPMC12938552

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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.