Evidence map›Paper›PMID 31181822›Full record

ArticlePolymers2019

The Use of Platelet-Rich Plasma to Promote Cell Recruitment into Low-Molecular-Weight Fucoidan-Functionalized Poly(Ester-Urea-Urethane) Scaffolds for Soft-Tissue Engineering.

Géraldine Rohman, Credson Langueh, Salah Ramtani, Jean-Jacques Lataillade, Didier Lutomski, Karim Senni, Sylvie Changotade

Abstract read
In one paragraph

Article in Polymers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 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

7 authors.

Géraldine RohmanTissue Engineering and Proteomics (TIP) team, CSPBAT UMR CNRS 7244, Université Paris 13, Sorbonne Paris Cité, 74 rue Marcel Cachin, 93000 Bobigny, France. geraldine.rohman@univ-paris13.fr.ORCID 0000-0003-3176-3476
Credson LanguehTissue Engineering and Proteomics (TIP) team, CSPBAT UMR CNRS 7244, Université Paris 13, Sorbonne Paris Cité, 74 rue Marcel Cachin, 93000 Bobigny, France. credsonlangueh@gmail.com.
Salah RamtaniLBPS team, CSPBAT UMR CNRS 7244, Université Paris 13, Sorbonne Paris Cité, 99 avenue Jean-Baptiste Clément, 93430 Villetaneuse, France. ramtani@univ-paris13.fr.ORCID 0000-0002-4873-7584
Jean-Jacques LatailladeInstitut de Recherche Biomédicale des Armées, Unité de Thérapie Cellulaire et Réparation Tissulaire, Site du Centre de Transfusion Sanguine des Armées "Jean Julliard" de Clamart, BP 73, 91223 Brétigny-sur-Orge Cedex, France. jjlataillade@gmail.com.
Didier LutomskiTissue Engineering and Proteomics (TIP) team, CSPBAT UMR CNRS 7244, Université Paris 13, Sorbonne Paris Cité, 74 rue Marcel Cachin, 93000 Bobigny, France. lutomski@univ-paris13.fr.
Karim SenniEcole de biologie Industrielle, 49 avenue des Genottes, 95885 Cergy Cedex, France. senni_k@yahoo.com.
Sylvie ChangotadeTissue Engineering and Proteomics (TIP) team, CSPBAT UMR CNRS 7244, Université Paris 13, Sorbonne Paris Cité, 74 rue Marcel Cachin, 93000 Bobigny, France. changotade@univ-paris13.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Due to their elastomeric behavior, polyurethane-based scaffolds can find various applications in soft-tissue engineering. However, their relatively inert surface has to be modified in order to improve cell colonization and control cell fate. The present study focuses on porous biodegradable scaffolds based on poly(ester-urea-urethane), functionalized concomitantly to the scaffold elaboration with low-molecular-weight (LMW) fucoidan; and their bio-activation with platelet rich plasma (PRP) formulations with the aim to promote cell response. The LMW fucoidan-functionalization was obtained in a very homogeneous way, and was stable after the scaffold sterilization and incubation in phosphate-buffered saline. Biomolecules from PRP readily penetrated into the functionalized scaffold, leading to a biological frame on the pore walls. Preliminary in vitro assays were assessed to demonstrate the improvement of scaffold behavior towards cell response. The scaffold bio-activation drastically improved cell migration. Moreover, cells interacted with all pore sides into the bio-activated scaffold forming cell bridges across pores. Our work brought out an easy and versatile way of developing functionalized and bio-activated elastomeric poly(ester-urea-urethane) scaffolds with a better cell response.

Indexed as

fucoidanpoly(ester-urea-urethane)PRPscaffoldtissue engineering

Identifiers

PMID31181822
PMCPMC6631166

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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.