Evidence map›Paper›PMID 34960825›Full record

ArticlePolymers2021

Development of a New Formulation Based on In Situ Photopolymerized Polymer for the Treatment of Spinal Cord Injury.

Gabrielle B Novais, Stefane Dos Santos, Robertta J R Santana, Rose N P Filho, John L S Cunha, Bruno S Lima, Adriano A S Araújo, Patricia Severino, Ricardo L C Albuquerque Júnior, Juliana C Cardoso and 2 more

Open access · goldAbstract read
In one paragraph

Article in Polymers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Formononetin: A Pathway to Protect Neurons.Frontiers in integrative neuroscience · 2022
    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

12 authors at 6 institutions in 2 countries.

Gabrielle B NovaisHealth and Environment Postgraduate Program, Tiradentes University, Aracaju 49032 490, Sergipe, Brazil.
Stefane Dos SantosBiomedicine Graduation Program, Tiradentes University, Aracaju 49032 490, Sergipe, Brazil.
Robertta J R SantanaSchool of Pharmacy, Tiradentes University, Aracaju 49032 490, Sergipe, Brazil.
Rose N P FilhoLaboratory of Morphology and Experimental Pathology (LMBE), Institute of Technology and Research (ITP), Tiradentes University, Aracaju 49032 490, Sergipe, Brazil.
John L S CunhaDepartment of Odontology, Paraiba State University, Campina Grande 58429 500, Paraíba, Brazil.
Bruno S LimaDepartment of Pharmaceutical Sciences, Federal University of Sergipe, São Cristóvão 49000 100, Sergipe, Brazil.
Adriano A S AraújoDepartment of Pharmaceutical Sciences, Federal University of Sergipe, São Cristóvão 49000 100, Sergipe, Brazil.
Patricia SeverinoNanomedicine and Nanotechnology Laboratory (LNMed), Institute of Technology and Research (ITP), Av. Murilo Dantas, 300, Aracaju 49010 390, Sergipe, Brazil.ORCID 0000-0001-6527-6612
Ricardo L C Albuquerque JúniorLaboratory of Morphology and Experimental Pathology (LMBE), Institute of Technology and Research (ITP), Tiradentes University, Aracaju 49032 490, Sergipe, Brazil.
Juliana C CardosoLaboratory of Biomaterials (LBmat), Institute of Technology and Research (ITP), Av. Murilo Dantas, 300, Aracaju 49010 390, Sergipe, Brazil.ORCID 0000-0002-0357-4144
Eliana B SoutoCEB-Centre of Biological Engineering, Campus de Gualtar, University of Minho, 4710-057 Braga, Portugal.ORCID 0000-0002-9737-6017
Margarete Z GomesLaboratory of Morphology and Experimental Pathology (LMBE), Institute of Technology and Research (ITP), Tiradentes University, Aracaju 49032 490, Sergipe, Brazil.
Instituto de Tecnologia e Pesquisa · BRUniversidade Tiradentes · BRUniversidade Federal de Sergipe · BRNanomed (Brazil) · BRUniversidade Estadual da Paraíba · BRUniversity of Minho · PT

Funding

Banco do Nordeste (grant FUNDECI/2016.0015), National Council for Scientific and Technological (CNPq), Research and Technological Innovation Support Foundation of the State of Sergipe (Fapitec) and Coordination for the Improvement of Higher Education Pers grant FUNDECI/2016.0015; 309458/2019-6, 301964/2019-0, 312451/2021/2, UIDB/04469/2020
6 · The paper itself

Abstract

Spinal Cord Injury (SCI) promotes a cascade of inflammatory events that are responsible for neuronal death and glial scar formation at the site of the injury, hindering tissue neuroregeneration. Among the main approaches for the treatment of SCI, the use of biomaterials, especially gelatin methacryloyl (GelMA), has been proposed because it is biocompatible, has excellent mechanical properties, favoring cell adhesion and proliferation. In addition, it can act as a carrier of anti-inflammatory drugs, preventing the formation of glial scars. The present work presents the development and in situ application of a light-curing formulation based on GelMA containing a natural extract rich in anti-inflammatory, antioxidant and neuroprotective substances (hydroalcoholic extract of red propolis-HERP) in an experimental model of SCI in rats. The formulations were prepared and characterized by time of UV exposition, FTIR, swelling and degradation. The hydrogels containing 1 mg/mL of HERP were obtained by the exposure to UV radiation of 2 μL of the formulation for 60 s. The locomotor evaluation of the animals was performed by the scale (BBB) and demonstrated that after 3 and 7 days of the injury, the GelMA-HERP group (BBB = 5 and 7) presented greater recovery compared to the GelMA group (BBB = 4 and 5). Regarding the inflammatory process, using histomorphological techniques, there was an inflammation reduction in the groups treated with GelMA and GelMA-HERP, with decreases of cavitation in the injury site. Therefore, it is possible to conclude that the use of GelMA and GelMA-HERP hydrogel formulations is a promising strategy for the treatment of SCI when applied in situ, as soon as possible after the injury, improving the clinical and inflammatory conditions of the treated animals.

Indexed as

flavonoidsformononetinmethacryloyl gelatinred propolisspinal cord injury

Identifiers

PMID34960825
PMCPMC8705720
OpenAlexW4200045327

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.