Evidence map›Paper›PMID 26556578›Full record

ArticleClinical oral investigations2016

Evaluation of carbon nanotubes functionalized with sodium hyaluronate in the inflammatory processes for oral regenerative medicine applications.

Paulo Antônio Martins-Júnior, Marcos Augusto Sá, Alesandra Corte Reis, Celso Martins Queiroz-Junior, Marcelo Vidigal Caliari, Mauro Martins Teixeira, Luiz Orlando Ladeira, Vanessa Pinho, Anderson José Ferreira

Abstract read
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In one paragraph

Article in Clinical oral investigations, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

3 citing papers in PubMed, 12 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

9 authors at 1 institution in 1 country.

Paulo Antônio Martins-JúniorDepartment of Morphology, Biological Sciences Institute, Federal University of Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, 31.270-901, MG, Brazil.
Marcos Augusto SáDepartment of Morphology, Biological Sciences Institute, Federal University of Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, 31.270-901, MG, Brazil.
Alesandra Corte ReisDepartment of Morphology, Biological Sciences Institute, Federal University of Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, 31.270-901, MG, Brazil.
Celso Martins Queiroz-JuniorDepartment of Morphology, Biological Sciences Institute, Federal University of Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, 31.270-901, MG, Brazil.
Marcelo Vidigal CaliariDepartment of General Pathology, Biological Sciences Institute, Federal University of Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, 31.270-901, MG, Brazil.
Mauro Martins TeixeiraDepartment of Biochemistry and Immunology, Biological Sciences Institute, Federal University of Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, 31.270-901, MG, Brazil.
Luiz Orlando LadeiraDepartment of Physics, Institute of Exact Sciences, Federal University of Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, 31.270-901, MG, Brazil.
Vanessa PinhoDepartment of Morphology, Biological Sciences Institute, Federal University of Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, 31.270-901, MG, Brazil.
Anderson José FerreiraDepartment of Morphology, Biological Sciences Institute, Federal University of Minas Gerais, Av. Antônio Carlos 6627, Belo Horizonte, 31.270-901, MG, Brazil. anderson@icb.ufmg.br.
Universidade Federal de Minas Gerais · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe objectives of this study were to assess the effects of hyaluronic acid (HY), multi-walled carbon nanotubes (MWCNT), and MWCNT functionalized with HY (HY-MWCNT) on the resolution of neutrophilic inflammation in the pleural cavity of LPS-challenged mice and to assess the influence of these materials in the inflammatory process of bone repair of tooth sockets of rats. MATERIALS AND

methodsC57Bl/6 mice were intra-pleurally injected with HY, MWCNT, HY-MWCNT, phosphate-buffered saline (PBS), or LPS. The animals were euthanized after 8 and 24 h, and cells were harvested for total and differential cell counting. The tooth sockets of Wistar rats were filled with HY, MWCNT, HY-MWCNT, or blood clot (control). After 1, 3, and 7 days, histological and morphometric analyses evaluated the number of cell nuclei and blood vessels, and bone trabeculae formation in the sockets. Myeloperoxidase (MPO) activity quantified neutrophil accumulation in the sockets.

resultsHY, MWCNT, and HY-MWCNT increased neutrophilic recruitment at 8 h and reduced the inflammatory process at 24 h in the pleural cavity. Histological and morphometric analyses and MPO activity showed no significant differences in the recruitment of inflammatory cells in the tooth sockets. HY increased the number of blood vessels, and HY and HY-MWCNT increased bone trabeculae formation at 7 days of tooth extraction.

conclusionsHY, MWCNT, and HY-MWCNT resolved the neutrophilic inflammation in the pleural cavity of the mice. However, these materials did not modulate the inflammatory process in the early stages of bone repair of the tooth sockets, thereby excluding this action as a possible mechanism by which these biomaterials accelerate bone repair. CLINICAL RELEVANCE: HY-MWCNT is capable of accelerating bone repair/regeneration without affecting the inflammatory phase during the bone healing process.

Indexed as

Nanotubes, CarbonAnimalsCell MovementHyaluronic AcidInflammationLeukocytesMaleMiceMice, Inbred C57BLPeroxidaseRatsRats, WistarRegenerative MedicineTooth SocketWound HealingHyaluronic AcidNanotubes, CarbonPeroxidaseBone repairCarbon nanotubesHyaluronic acidInflammationNeutrophil

Identifiers

PMID26556578
OpenAlexW2235686819

What OpenQuestion holds

Textmetadata
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.