Evidence map›Paper›PMID 35479903›Full record

ArticleRSC advances2021

Design of graphenic nanocomposites containing chitosan and polyethylene glycol for spinal cord injury improvement.

Ayda Yari-Ilkhchi, Abbas Ebrahimi-Kalan, Mehdi Farhoudi, Mehrdad Mahkam

Abstract read
In one paragraph

Article in RSC advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Spinal cord injury: molecular mechanisms and therapeutic interventions.Signal transduction and targeted therapy · 2023
    Review
  9. Review
  10. Review
  11. The Application of Biomaterials in Spinal Cord Injury.International journal of molecular sciences · 2023
    Review
  12. Article
  13. Review
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

4 authors.

Ayda Yari-IlkhchiChemistry Department, Faculty of Science, Azarbaijan Shahid Madani University Tabriz Iran mmahkam@yahoo.com mmahkam@gmail.com mahkam@azaruniv.ac.ir +98 4134327541.ORCID https://orcid.org/0000-0002-0582-2850
Abbas Ebrahimi-KalanFaculty of Advanced Medical Science, Tabriz University of Medical Sciences Tabriz Iran.ORCID https://orcid.org/0000-0001-5466-6754
Mehdi FarhoudiNeurosciences Research Center (NSRC), Tabriz University of Medical Science Tabriz Iran.ORCID https://orcid.org/0000-0002-4972-9316
Mehrdad MahkamChemistry Department, Faculty of Science, Azarbaijan Shahid Madani University Tabriz Iran mmahkam@yahoo.com mmahkam@gmail.com mahkam@azaruniv.ac.ir +98 4134327541.ORCID https://orcid.org/0000-0001-9335-6257

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advanced therapeutic strategies include the incorporation of biomaterials, which has been identified as an effective method in treating unsolved diseases, such as spinal cord injury. During the acute phase, cascade responses involving cystic cavitation, fibrous glial scar formation, and myelin-associated dissuasive accumulation occur in the microenvironment of the spinal cord lesion. Graphene oxide (GO)-based materials, due to their extraordinary chemical, electrical and mechanical properties and easy to modify structure, are considered as rising stars in biomaterial and tissue engineering. In order to enhance the biodegradability and biocompatibility of GO, cell proliferation may be appropriately designed and situated at the lesion site. In this study, chitosan (CS) and polyethylene glycol (PEG) were grafted onto GO sheets. CS is a natural non-toxic polymer with good solubility and high biocompatible potential that has been used as an anti-inflammatory and anti-oxidant agent. Furthermore, PEG, a synthetic neuroprotective polymer, was used to develop the pharmacokinetic activity and reduce the toxicity of GO. Herein we report a novel nanocomposite consisting of PEG and CS with a potential advantage in spinal tissue regeneration. The preliminary

Identifiers

PMID35479903
PMCPMC9033813

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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.