Evidence map›Paper›PMID 31734793›Full record

ArticleClinical oral investigations2020

Flexural strength, biocompatibility, and antimicrobial activity of a polymethyl methacrylate denture resin enhanced with graphene and silver nanoparticles.

Cecilia Bacali, Ioana Baldea, Marioara Moldovan, Rahela Carpa, Diana Elena Olteanu, Gabriela Adriana Filip, Vivi Nastase, Liana Lascu, Mandra Badea, Mariana Constantiniuc and 1 more

Abstract read
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In one paragraph

Article in Clinical oral investigations, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 5% 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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 115 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

11 authors at 3 institutions in 2 countries.

Cecilia BacaliDepartment of Prosthodontics and Dental Materials, Iuliu Hatieganu University of Medicine and Pharmacy, Clinicilor, 32, Cluj-Napoca, Romania.
Ioana BaldeaDepartment of Physiology, Iuliu Hatieganu University of Medicine and Pharmacy, Clinicilor 1, Cluj-Napoca, Romania. baldeaioana@gmail.com.ORCID http://orcid.org/0000-0003-4046-7310
Marioara MoldovanRaluca Ripan Institute for Research in Chemistry, Babeș Bolyai University, Fantanele 30, Cluj-Napoca, Romania.
Rahela CarpaFaculty of Biology and Geology, Department of Molecular Biology and Biotechnology, Babeș Bolyai University, M. Kogălniceanu 1, 400084, Cluj-Napoca, Romania.
Diana Elena OlteanuDepartment of Physiology, Iuliu Hatieganu University of Medicine and Pharmacy, Clinicilor 1, Cluj-Napoca, Romania.
Gabriela Adriana FilipDepartment of Physiology, Iuliu Hatieganu University of Medicine and Pharmacy, Clinicilor 1, Cluj-Napoca, Romania.
Vivi NastaseInstitute for Computational Linguistics, University of Heidelberg, Im Neuenheimerfeld 325, 69120, Heidelberg, Germany.
Liana LascuDepartment of Prosthodontics and Dental Materials, Iuliu Hatieganu University of Medicine and Pharmacy, Clinicilor, 32, Cluj-Napoca, Romania.
Mandra BadeaDepartment of Preventive Dental Medicine, Iuliu Hatieganu University of Medicine and Pharmacy, Avram Iancu 31, Cluj-Napoca, Romania.
Mariana ConstantiniucDepartment of Prosthodontics and Dental Materials, Iuliu Hatieganu University of Medicine and Pharmacy, Clinicilor, 32, Cluj-Napoca, Romania. mconstantiniuc@umfcluj.ro.
Florin BadeaDepartment, of Anatomy and Embryology, Iuliu Hatieganu University of Medicine and Pharmacy, Clinicilor 3-5, Cluj-Napoca, Romania.
Iuliu Hațieganu University of Medicine and Pharmacy · ROBabeș-Bolyai University · ROHeidelberg University · DE

Funding

Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, Romania PCD 7690/76/15.04.2016
6 · The paper itself

Abstract

objectiveThe study evaluates the effect of adding graphene-Ag nanoparticles (G-AgNp) to a PMMA auto-polymerizing resin, with focus on antibacterial activity, cytotoxicity, monomer release, and mechanical properties. MATERIALS AND

methodsAuto-polymerizing acrylic resin (M) was loaded with 1 wt% G-AgNp (P1) and 2 wt% G-AgNp (P2). Methyl methacrylate monomer release (MMA) was measured after immersion of the samples in chloroform and cell medium respectively. Cell viability was assessed on dysplastic oral keratinocytes (DOK) and dental pulp stem cells. Oxidative stress and inflammatory response following exposure of dysplastic oral keratinocytes to the experimental resins was evaluated. Antibacterial activity against Staphylococcus aureus, Streptococcus mutans and Escherichia coli and also flexural strength of the resins were assessed.

resultsResidual monomer: For samples immersed in chloroform, MMA concentration reached high levels, 10.27 μg/g for sample P1; MMA increased at higher G-AgNp loading; 0.63 μg/g MMA was found in medium for P1, and less for sample P2. Cell viability: Both cell lines displayed a viability decrease, but remained above 75%, compared to controls, when exposed to undiluted samples. Inflammation: proinflammatory molecule TNF-α decreased when DOK cultures were exposed to G-AgNp samples. MDA levels indicated increased oxidative stress damage in cells treated with PMMA, confirmed by the antioxidant mechanism activation, while samples containing G-AgNp induced an antioxidant effect. All tested samples showed antibacterial properties against Gram-positive bacteria. Samples containing G-AgNp also exhibited bactericide action on E. coli. Mechanical properties: both samples containing G-AgNp improved flexural strength compared to the sample resin, measured through elastic strength parameters.

conclusionsPMMA resin loaded with G-AgNp presents promising antibacterial activity associated with minimal toxicity to human cells, in vitro, as well as improved flexural properties. CLINICAL RELEVANCE: These encouraging results obtained in vitro support further in vivo investigation, to thoroughly check whether the PMMA loaded with graphene-silver nanoparticles constitute an improvement over current denture materials.

Indexed as

Metal NanoparticlesAnti-Infective AgentsDenture BasesDenturesEscherichia coliFlexural StrengthGraphiteHumansMaterials TestingPolymethyl MethacrylateSilverAnti-Infective AgentsGraphitePolymethyl MethacrylateSilverAntibacterial actionBiocompatibilityGraphenePMMA resinSilver nanoparticles

Identifiers

PMID31734793
OpenAlexW2987956912

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.