Evidence map›Paper›PMID 32421748›Full record

ArticlePloS one2020

Graphene-based 2D constructs for enhanced fibroblast support.

Ingrid Safina, Shawn E Bourdo, Karrer M Algazali, Ganesh Kannarpady, Fumiya Watanabe, Kieng Bao Vang, Alexandru S Biris

Abstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
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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.

Ingrid SafinaCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, United States of America.ORCID 0000-0003-1036-1101
Shawn E BourdoCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, United States of America.
Karrer M AlgazaliCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, United States of America.
Ganesh KannarpadyCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, United States of America.
Fumiya WatanabeCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, United States of America.
Kieng Bao VangCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, United States of America.
Alexandru S BirisCenter for Integrative Nanotechnology Sciences, University of Arkansas at Little Rock, Little Rock, AR, United States of America.

Funding

Bone regeneration: mesenchymal stem cells and graphene biomimetic nanomaterialsR15AR070460 · NIAMS · UNIVERSITY OF TENNESSEE KNOXVILLE · PI DHAR, MADHU S · 2018 to 2018
$427k
NIAMS NIH HHS R15 AR070460
6 · The paper itself

Abstract

Complex skin wounds have always been a significant health and economic problem worldwide due to their elusive and sometimes poor or non-healing conditions. If not well-treated, such wounds may lead to amputation, infections, cancer, or even death. Thus, there is a need to efficiently generate multifunctional skin grafts that address a wide range of skin conditions, including non-healing wounds, and enable the regeneration of new skin tissue. Here, we propose studying pristine graphene and two of its oxygen-functionalized derivatives-high and low-oxygen graphene films-as potential substrates for skin cell proliferation and differentiation. Using BJ cells (human foreskin-derived fibroblasts) to represent basic skin cells, we show that the changes in surface properties of pristine graphene due to oxygen functionalization do not seem to statistically impact the normal proliferation and maturation of skin cells. Our results indicate that the pristine and oxidized graphenes presented relatively low cytotoxicity to BJ fibroblasts and, in fact, support their growth and bioactivity. Therefore, these graphene films could potentially be integrated into more complex skin regenerative systems to support skin regeneration. Because graphene's surface can be relatively easily functionalized with various chemical groups, this finding presents a major opportunity for the development of various composite materials that can act as active components in regenerative applications such as skin regeneration.

Indexed as

Cell LineCell ProliferationCell SurvivalFibroblastsGraphiteHumansSurface PropertiesTissue EngineeringTissue Scaffoldsgraphene oxideGraphite

Identifiers

PMID32421748
PMCPMC7233589

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.