Evidence map›Paper›PMID 40621679›Full record

ArticleACS applied materials & interfaces2025

Long-Gap Sciatic Nerve Regeneration Using 3D-Printed Nerve Conduits with Controlled FGF-2 Release.

Diego N Rodriguez-Sanchez, Leticia A M de Carvalho, Ingri Mancilla-Corzo, Luciana P Cartarozzi, Saeed Safari, Menekse Ermis, Marcos A d'Ávila, Alexandre L R Oliveira

Abstract read
In one paragraph

Article in ACS applied materials & interfaces, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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.

Diego N Rodriguez-SanchezLaboratory of Nerve Regeneration, Department of Structural and Functional Biology, Institute of Biology, University of Campinas (UNICAMP), Campinas, Sao Paulo 13083-970, Brazil.ORCID 0000-0001-6524-5939
Leticia A M de CarvalhoLaboratory of Nerve Regeneration, Department of Structural and Functional Biology, Institute of Biology, University of Campinas (UNICAMP), Campinas, Sao Paulo 13083-970, Brazil.
Ingri Mancilla-CorzoDepartment of Manufacturing and Materials Engineering, School of Mechanical Engineering, University of Campinas (UNICAMP), Campinas, Sao Paulo 13083-860, Brazil.ORCID 0000-0001-6181-7290
Luciana P CartarozziLaboratory of Nerve Regeneration, Department of Structural and Functional Biology, Institute of Biology, University of Campinas (UNICAMP), Campinas, Sao Paulo 13083-970, Brazil.
Saeed SafariTerasaki Institute for Biomedical Innovation (TIBI), Woodland Hills, California 91367, United States.
Menekse ErmisTerasaki Institute for Biomedical Innovation (TIBI), Woodland Hills, California 91367, United States.
Marcos A d'ÁvilaDepartment of Manufacturing and Materials Engineering, School of Mechanical Engineering, University of Campinas (UNICAMP), Campinas, Sao Paulo 13083-860, Brazil.
Alexandre L R OliveiraLaboratory of Nerve Regeneration, Department of Structural and Functional Biology, Institute of Biology, University of Campinas (UNICAMP), Campinas, Sao Paulo 13083-970, Brazil.ORCID 0000-0003-4224-4575

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peripheral nerve injuries (PNIs) by transection require reconstructive surgery, often with highly variable results and persistent sensory and motor deficits. Three-dimensional (3D) printing enables the biofabrication of nerve guidance conduits (NGCs) with the ability to release neurotrophic factors, showing therapeutic potential. We developed a 3D printing process of NGCs using polycaprolactone (PCL) and gelatin methacryloyl (GelMA) integrated with a thermostable fibroblast growth factor 2 (FGF-2). The synthesized GelMA at 10% (w/v) concentration showed superior rheological, mechanical, and ultrastructural characteristics, ensuring 3D printing fidelity. Incorporating FGF-2 into GelMA resulted in a controlled release pattern over 30 days along with biocompatibility and an increase of metabolism in rat S16 Schwann cells and human mesenchymal stem cells (MSCs). MSCs exhibited gene regulation linked to vascularization after FGF-2 stimulation. The PCL polymer facilitated the buildability of a spiral-patterned tubular structure, which was functionalized with a combination of GelMA and UV photocrosslinked. At 12 weeks, following a long-gap nerve injury in rats, NGC implantation enhanced sensory and motor recovery, improved electrophysiological function, and promoted morphological and ultrastructural nerve reorganization and regeneration. At 4 weeks, significant Schwann cell proliferation (S100), expression of the pan-neurotrophin receptor (P75NTR), myelination of newly grown axons, and organization of neurofilaments were observed. The bioactive NGCs represent a promising alternative to nerve autografts for the repair of long-gap injuries.

Indexed as

Fibroblast Growth Factor 2Nerve RegenerationPeripheral Nerve InjuriesPrinting, Three-DimensionalSciatic NerveAnimalsGelatinHumansMaleMesenchymal Stem CellsMethacrylatesPolyestersRatsRats, Sprague-DawleySchwann CellsTissue ScaffoldsFibroblast Growth Factor 2Gelatingelatin methacryloylMethacrylatespolycaprolactonePolyesters3D printingbiomaterialsFGF-2gelatin methacryloylnerve guidance conduitsperipheral nerve regenerationpolycaprolactone

Identifiers

PMID40621679
PMCPMC12278209

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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.