Evidence map›Paper›PMID 28183673›Full record

ArticleMaterials science & engineering. C, Materials for biological applications2017

Attenuation of the in vitro neurotoxicity of 316L SS by graphene oxide surface coating.

Nishat Tasnim, Alok Kumar, Binata Joddar

Abstract read
In one paragraph

Article in Materials science & engineering. C, Materials for biological applications, 2017. 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
  2. Article
  3. Article
  4. Surface Area of Graphene Governs Its Neurotoxicity.ACS biomaterials science & engineering · 2023
    Article
  5. Article
  6. Article
  7. The applicability of furfuryl-gelatin as a novel bioink for tissue engineering applications.Journal of biomedical materials research. Part B, Applied biomaterials · 2019
    Article
  8. Review
  9. 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

3 authors.

Nishat TasnimDepartment of Metallurgical, Materials Science and Biomedical Engineering, The University of Texas at El Paso, 500 W University Avenue, El Paso, TX 79968, USA.
Alok KumarDepartment of Metallurgical, Materials Science and Biomedical Engineering, The University of Texas at El Paso, 500 W University Avenue, El Paso, TX 79968, USA.
Binata JoddarDepartment of Metallurgical, Materials Science and Biomedical Engineering, The University of Texas at El Paso, 500 W University Avenue, El Paso, TX 79968, USA. Electronic address: bjoddar@utep.edu.

Funding

Phase II of BUILDing SCHOLARSUL1GM118970 · NIGMS · UNIVERSITY OF TEXAS EL PASO · PI ALEY, STEPHEN B, BOLAND, THOMAS · 2015 to 2023
$17.9M
Bioprinting of human iPSCs to facilitate their differentiation, recruitment and strategic assembly to form engineered cardiac patchesSC2HL134642 · NHLBI · UNIVERSITY OF TEXAS EL PASO · PI JODDAR, BINATA · 2016 to 2018
$438k
BUILDing SCHOLARS (Research Enrichment Core)RL5MD009592 · NIMHD · UNIVERSITY OF TEXAS EL PASO · PI AGUILERA, RENATO J, ALEY, STEPHEN B · 2014 to 2014
$268k
NHLBI NIH HHS SC2 HL134642NIGMS NIH HHS UL1 GM118970
6 · The paper itself

Abstract

A persistent theme in biomaterials research comprises of surface engineering and modification of bare metallic substrates for improved cellular response and biocompatibility. Graphene Oxide (GO), a derivative of graphene, has outstanding chemical and mechanical properties; its large surface to volume ratio, ease of surface modification and processing make GO an attractive coating material. GO-coatings have been extensively studied as biosensors. Further owing to its surface nano-architecture, GO-coated surfaces promote cell adhesion and growth, making it suitable for tissue engineering applications. The need to improve the long-term durability and therapeutic effectiveness of commercially available bare 316L stainless steel (SS) surfaces led us to adopt a polymer-free approach which is cost-effective and scalable. GO was immobilized on to 316L SS utilizing amide linkage, to generate a strongly adherent uniform coating with surface roughness. GO-coated 316L SS surfaces showed increased hydrophilicity and biocompatibility with SHSY-5Y neuronal cells, which proliferated well and showed decreased reactive oxygen species (ROS) expression. In contrast, cells did not adhere to bare uncoated 316L SS meshes nor maintain viability when cultured in the vicinity of bare meshes. Therefore the combination of the improved surface properties and biocompatibility implies that GO-coating can be utilized to overcome pertinent limitations of bare metallic 316L SS implant surfaces, especially SS neural electrodes. Also, the procedure for making GO-based protective coatings can be applied to numerous other implants where the development of such protective films is necessary.

Indexed as

Cell AdhesionCell Line, TumorCell ProliferationCoated Materials, BiocompatibleElastic ModulusGraphiteHardnessHumansHydrophobic and Hydrophilic InteractionsIronMaterials TestingNeurotoxinsPropylaminesReproducibility of ResultsSilanesSpectroscopy, Fourier Transform Infraredamino-propyl-triethoxysilaneCoated Materials, BiocompatibleGraphiteIronNeurotoxinsPropylaminesSilanesStainless SteelSUS 316LBiocompatibilityGraphene oxideNeuronal cellsStainless steel implantsSurface coating

Identifiers

PMID28183673
PMCPMC5312756

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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.