Evidence map›Paper›PMID 38137558›Full record

ArticleBiomedicines2023

Engineering 3D-Printed Bioresorbable Scaffold to Improve Non-Vascularized Fat Grafting: A Proof-of-Concept Study.

Amélia Jordao, Damien Cléret, Mélanie Dhayer, Mégann Le Rest, Shengheng Cao, Alexandre Rech, Nathalie Azaroual, Anne-Sophie Drucbert, Patrice Maboudou, Salim Dekiouk and 4 more

Open access · goldAbstract read
In one paragraph

Article in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 25% of its field
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

4 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
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

14 authors at 4 institutions in 1 country.

Amélia JordaoUMR9020-UMR-S 1277-Canther-Cancer Heterogeneity, Plasticity and Resistance to Therapies, CNRS, Inserm, CHU Lille, Oncolille, University Lille, F-59000 Lille, France.
Damien CléretLattice Medical, 80 rue du Docteur Yersin, F-59120 Loos, France.
Mélanie DhayerUMR9020-UMR-S 1277-Canther-Cancer Heterogeneity, Plasticity and Resistance to Therapies, CNRS, Inserm, CHU Lille, Oncolille, University Lille, F-59000 Lille, France.
Mégann Le RestLattice Medical, 80 rue du Docteur Yersin, F-59120 Loos, France.
Shengheng CaoLattice Medical, 80 rue du Docteur Yersin, F-59120 Loos, France.
Alexandre RechUniversity of Lille, Faculté de Pharmacie, Plateau RMN, UFR3S, F-59000 Lille, France.
Nathalie AzaroualUniversity of Lille, ULR 7365-GRITA-Groupe de Recherche Sur Les Formes Injectables Et Les Technologies Associées, F-59000 Lille, France.
Anne-Sophie DrucbertU 1008 Controlled Drug Delivery Systems and Biomaterials, Inserm, F-59000 Lille, France.
Patrice MaboudouService de Biochimie, CHU Lille, F-59000 Lille, France.
Salim DekioukUMR9020-UMR-S 1277-Canther-Cancer Heterogeneity, Plasticity and Resistance to Therapies, CNRS, Inserm, CHU Lille, Oncolille, University Lille, F-59000 Lille, France.
Nicolas GermainUMR9020-UMR-S 1277-Canther-Cancer Heterogeneity, Plasticity and Resistance to Therapies, CNRS, Inserm, CHU Lille, Oncolille, University Lille, F-59000 Lille, France.
Julien PayenLattice Medical, 80 rue du Docteur Yersin, F-59120 Loos, France.
Pierre GuerreschiU 1008 Controlled Drug Delivery Systems and Biomaterials, Inserm, F-59000 Lille, France.
Philippe MarchettiUMR9020-UMR-S 1277-Canther-Cancer Heterogeneity, Plasticity and Resistance to Therapies, CNRS, Inserm, CHU Lille, Oncolille, University Lille, F-59000 Lille, France.ORCID 0000-0002-4663-6800
Centre National de la Recherche Scientifique · FRInserm · FRUniversité de Lille · FRCentre Hospitalier Universitaire de Lille · FR

Funding

Association des Gueules Cassées XXXFrench Defense Innovation Agency through the RAPID program Hypofill
6 · The paper itself

Abstract

Autologous fat grafting is the gold standard for treatment in patients with soft-tissue defects. However, the technique has a major limitation of unpredictable fat resorption due to insufficient blood supply in the initial phase after transplantation. To overcome this problem, we investigated the capability of a medical-grade poly L-lactide-co-poly ε-caprolactone (PLCL) scaffold to support adipose tissue and vascular regeneration. Deploying FDM 3D-printing, we produced a bioresorbable porous scaffold with interconnected pore networks to facilitate nutrient and oxygen diffusion. The compressive modulus of printed scaffold mimicked the mechanical properties of native adipose tissue. In vitro assays demonstrated that PLCL scaffolds or their degradation products supported differentiation of preadipocytes into viable mature adipocytes under appropriate induction. Interestingly, the chorioallantoic membrane assay revealed vascular invasion inside the porous scaffold, which represented a guiding structure for ingrowing blood vessels. Then, lipoaspirate-seeded scaffolds were transplanted subcutaneously into the dorsal region of immunocompetent rats (

Indexed as

3D printingautologous fat graftingbiomaterialschorioallantoic membranetissue engineeringvascularization

Identifiers

PMID38137558
PMCPMC10741522
OpenAlexW4389917529

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.