Evidence map›Paper›PMID 34502249›Full record

ArticleInternational journal of molecular sciences2021

Anisotropic Chitosan Scaffolds Generated by Electrostatic Flocking Combined with Alginate Hydrogel Support Chondrogenic Differentiation.

Elke Gossla, Anne Bernhardt, Robert Tonndorf, Dilbar Aibibu, Chokri Cherif, Michael Gelinsky

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. 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
3.1field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Elke GosslaCentre for Translational Bone, Joint and Soft Tissue Research, University Hospital and Faculty of Medicine, Technische Universität Dresden, D-01307 Dresden, Germany.ORCID 0000-0002-6669-2797
Anne BernhardtCentre for Translational Bone, Joint and Soft Tissue Research, University Hospital and Faculty of Medicine, Technische Universität Dresden, D-01307 Dresden, Germany.ORCID 0000-0002-1903-1929
Robert TonndorfInstitute of Textile Machinery and High Performance Material Technology, Technische Universität Dresden, D-01062 Dresden, Germany.ORCID 0000-0002-2379-2245
Dilbar AibibuInstitute of Textile Machinery and High Performance Material Technology, Technische Universität Dresden, D-01062 Dresden, Germany.
Chokri CherifInstitute of Textile Machinery and High Performance Material Technology, Technische Universität Dresden, D-01062 Dresden, Germany.
Michael GelinskyCentre for Translational Bone, Joint and Soft Tissue Research, University Hospital and Faculty of Medicine, Technische Universität Dresden, D-01307 Dresden, Germany.ORCID 0000-0001-9075-5121
Technische Universität Dresden · DE

Funding

Deutsche Forschungsgemeinschaft GE 1133/16-1
6 · The paper itself

Abstract

The replacement of damaged or degenerated articular cartilage tissue remains a challenge, as this non-vascularized tissue has a very limited self-healing capacity. Therefore, tissue engineering (TE) of cartilage is a promising treatment option. Although significant progress has been made in recent years, there is still a lack of scaffolds that ensure the formation of functional cartilage tissue while meeting the mechanical requirements for chondrogenic TE. In this article, we report the application of flock technology, a common process in the modern textile industry, to produce flock scaffolds made of chitosan (a biodegradable and biocompatible biopolymer) for chondrogenic TE. By combining an alginate hydrogel with a chitosan flock scaffold (CFS+ALG), a fiber-reinforced hydrogel with anisotropic properties was developed to support chondrogenic differentiation of embedded human chondrocytes. Pure alginate hydrogels (ALG) and pure chitosan flock scaffolds (CFS) were studied as controls. Morphology of primary human chondrocytes analyzed by cLSM and SEM showed a round, chondrogenic phenotype in CFS+ALG and ALG after 21 days of differentiation, whereas chondrocytes on CFS formed spheroids. The compressive strength of CFS+ALG was higher than the compressive strength of ALG and CFS alone. Chondrocytes embedded in CFS+ALG showed gene expression of chondrogenic markers (

Indexed as

AggrecansAlginatesAnisotropyBiocompatible MaterialsCartilage Oligomeric Matrix ProteinCell DifferentiationCell ProliferationChitosanChondrocytesChondrogenesisCollagenCollagen Type IICompressive StrengthFemaleGlycosaminoglycansHumansA73025ACAN protein, humanAggrecansAlginatesBiocompatible MaterialsCartilage Oligomeric Matrix ProteinChitosanCollagenCollagen Type IIGlycosaminoglycansHydrogelsTSP5 protein, humanalginatecartilagechitosanchondrocyteselectrostatic flocking

Identifiers

PMID34502249
PMCPMC8430627
OpenAlexW3198273237

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.