Evidence map›Paper›PMID 42182877›Full record

ArticleMaterials today. Bio2026

A proof-of-concept study of an albumin-based bilayered scaffold for cartilage regeneration.

Christelle Bertsch, Florent Colin, Eya Aloui, Julien Graff, Maria Cristina Antal, Sabine Kuchler-Bopp, Adrien Moya, Romy Marek, Sven Zaugg, Eric Mathieu and 9 more

Abstract read
In one paragraph

Article in Materials today. Bio, 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

19 authors.

Christelle BertschInserm UMR_S 1121, CNRS EMR 7003, Université de Strasbourg, Biomaterials and Bioengineering, Centre de Recherche en Biomédecine de Strasbourg, 1 Rue Eugène Boeckel, Strasbourg, F-67000, France.
Florent ColinInserm UMR_S 1121, CNRS EMR 7003, Université de Strasbourg, Biomaterials and Bioengineering, Centre de Recherche en Biomédecine de Strasbourg, 1 Rue Eugène Boeckel, Strasbourg, F-67000, France.
Eya AlouiALBUPAD SAS, 32 Allée de la Robertsau, Strasbourg, 67000, France.
Julien GraffInstitut d'histologie, Faculté de médecine, Université de Strasbourg, Strasbourg, France.
Maria Cristina AntalInstitut d'histologie, Faculté de médecine, Université de Strasbourg, Strasbourg, France.
Sabine Kuchler-BoppInserm UMR_S 1121, CNRS EMR 7003, Université de Strasbourg, Biomaterials and Bioengineering, Centre de Recherche en Biomédecine de Strasbourg, 1 Rue Eugène Boeckel, Strasbourg, F-67000, France.
Adrien MoyaDepartment of Biomedicine, University of Basel, University Hospital of Basel, Hebelstrasse 20, Basel, 4031, Switzerland.
Romy MarekUniversity of Applied Sciences Northwestern Switzerland FHNW, School of Life Sciences HLS, Institute for Medical Engineering and Medical Informatics IM2, Hofackerstrasse 30, Muttenz, 4132, Switzerland.
Sven ZauggUniversity of Applied Sciences Northwestern Switzerland FHNW, School of Life Sciences HLS, Institute for Medical Engineering and Medical Informatics IM2, Hofackerstrasse 30, Muttenz, 4132, Switzerland.
Eric MathieuInserm UMR_S 1121, CNRS EMR 7003, Université de Strasbourg, Biomaterials and Bioengineering, Centre de Recherche en Biomédecine de Strasbourg, 1 Rue Eugène Boeckel, Strasbourg, F-67000, France.
Claire ThibaultInserm UMR_S 1121, CNRS EMR 7003, Université de Strasbourg, Biomaterials and Bioengineering, Centre de Recherche en Biomédecine de Strasbourg, 1 Rue Eugène Boeckel, Strasbourg, F-67000, France.
Christian DebryInserm UMR_S 1121, CNRS EMR 7003, Université de Strasbourg, Biomaterials and Bioengineering, Centre de Recherche en Biomédecine de Strasbourg, 1 Rue Eugène Boeckel, Strasbourg, F-67000, France.
Jordan BeurtonInserm UMR_S 1121, CNRS EMR 7003, Université de Strasbourg, Biomaterials and Bioengineering, Centre de Recherche en Biomédecine de Strasbourg, 1 Rue Eugène Boeckel, Strasbourg, F-67000, France.
Bernard SengerInserm UMR_S 1121, CNRS EMR 7003, Université de Strasbourg, Biomaterials and Bioengineering, Centre de Recherche en Biomédecine de Strasbourg, 1 Rue Eugène Boeckel, Strasbourg, F-67000, France.
Benoit FrischInserm UMR_S 1121, CNRS EMR 7003, Université de Strasbourg, Biomaterials and Bioengineering, Centre de Recherche en Biomédecine de Strasbourg, 1 Rue Eugène Boeckel, Strasbourg, F-67000, France.
Michael de WildUniversity of Applied Sciences Northwestern Switzerland FHNW, School of Life Sciences HLS, Institute for Medical Engineering and Medical Informatics IM2, Hofackerstrasse 30, Muttenz, 4132, Switzerland.
Arnaud ScherberichDepartment of Biomedicine, University of Basel, University Hospital of Basel, Hebelstrasse 20, Basel, 4031, Switzerland.
Philippe LavalleInserm UMR_S 1121, CNRS EMR 7003, Université de Strasbourg, Biomaterials and Bioengineering, Centre de Recherche en Biomédecine de Strasbourg, 1 Rue Eugène Boeckel, Strasbourg, F-67000, France.
Léa FathInserm UMR_S 1121, CNRS EMR 7003, Université de Strasbourg, Biomaterials and Bioengineering, Centre de Recherche en Biomédecine de Strasbourg, 1 Rue Eugène Boeckel, Strasbourg, F-67000, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cartilage, particularly hyaline cartilage, is essential for structural and functional integrity in otorhinolaryngological region (nose, ears, larynx, and trachea) but exhibits limited regenerative capacity due to its avascular nature. Current clinical strategies, including microfracture, autologous chondrocyte implantation, and cartilage grafting remain limited by poor integration, donor site morbidity, and fibrocartilage formation rather than hyaline cartilage. In parallel, most clinically investigated scaffolds rely on xenogeneic collagen, raising concerns regarding batch-to-batch variability, immunogenicity, regulatory burden, and sourcing. Together, these limitations highlight the need for more clinically translatable autologous, biomimetic, and scalable biomaterials. Here, we report a proof-of-concept albumin-based bilayered scaffold for cartilage tissue engineering, using a salt-assisted compaction process without the use of chemical crosslinkers, based on albumin self-assembly. This scaffold combines a porous layer to support cell infiltration and cartilage-like formation, and a smooth layer to support later the regeneration of cutaneous (auricular) or respiratory (tracheal or nasal) epithelium in situ. In this study, human nasal chondrocytes seeded in the scaffold showed proliferation, maintained viability and were associated with the production of cartilage-like extracellular matrix rich in type II collagen and aggrecan. Following subcutaneous implantation in nude mice, the scaffold showed progressive degradation, tissue integration, and features consistent with hyaline-like cartilage formation. Overall, this work suggests that albumin-based bilayered scaffolds may represent a promising approach for cartilage repair and may be advantageous for applications in nasal, auricular, and craniofacial reconstruction. Further studies in orthotopic models will be required to evaluate their functional performance and clinical relevance.

Indexed as

AlbuminBilayered scaffoldsBiomaterialsBiomimetismMedical applicationsOtorhinolaryngologyTissue engineering

Identifiers

PMID42182877
PMCPMC13196399

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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.