Evidence map›Paper›PMID 21243381›Full record

ArticleClinical oral investigations2012

Oxidative stress and cytotoxicity generated by dental composites in human pulp cells.

Stephanie Krifka, Claudia Seidenader, Karl-Anton Hiller, Gottfried Schmalz, Helmut Schweikl

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Clinical oral investigations, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
9.5field-weighted citation impact, top 1% 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

40 citing papers in PubMed, 122 citations in OpenAlex.

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  4. Physicomechanical Properties and Morphological Characterization of Several Universal Resin Composites After Different Aging Procedures.Journal of esthetic and restorative dentistry : official publication of the American Academy of Esthetic Dentistry ... [et al.] · 2025
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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

5 authors at 2 institutions in 1 country.

Stephanie KrifkaDepartment of Operative Dentistry and Periodontology, University of Regensburg Medical Centre, Franz Josef Strauss Allee 11, 93042, Regensburg, Germany.
Claudia Seidenader
Karl-Anton Hiller
Gottfried Schmalz
Helmut Schweikl
University Hospital Regensburg · DEUniversity of Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dental composites are a source of residual monomers that are released into the oral environment. Since monomers act on cultured cells through reactive oxygen species (ROS), we hypothesized that composites generate ROS associated with cytotoxicity. Human pulp-derived cells were exposed to extracts of methacrylate-based materials including triethylene glycol dimethacrylate and 2-hydroxyethyl methacrylate-free composites (Tetric Ceram, Tetric EvoCeram, els, els flow, Solitaire 2) and a silorane-based composite (Hermes III). The materials were polymerized in the presence and absence of a polyester film and then extracted in culture medium. The generation of ROS was measured by flow cytometry, and cytotoxicity was determined as well. Methacrylate-based composites reduced cell survival but varied in efficiency. Undiluted extracts of Solitaire 2 specimens prepared in the absence of a polyester film reduced cell survival to 26% compared with untreated cultures. Cytotoxicity was reduced when specimens were covered with a polyester film during preparation. Cytotoxicity of the composites was ranked as follows: Solitaire 2 >> els flow > Tetric Ceram = Tetric EvoCeram = els > Hermes III. The generation of ROS followed the same pattern as detected with cytotoxic effects. A positive correlation was found between ROS production and cell survival caused by extracts made from materials not covered with a polyester film. These findings suggest that components released from composites affect cellular signaling networks through ROS formation. Regenerative and reparative capacities of the dentine-pulp complex may be impaired by biologically active resin monomers released from composite restorations.

Indexed as

Bisphenol A-Glycidyl MethacrylateCell Culture TechniquesCells, CulturedCell SurvivalColoring AgentsComposite ResinsDental MaterialsDental PulpFlow CytometryGentian VioletGlass Ionomer CementsHumansMethacrylatesOxidative StressPolyestersPolyethylene Glycols2,2-bis-(4-(2-methacryloxyethoxy)phenyl)propaneBisphenol A-Glycidyl MethacrylateColoring AgentsComposite ResinsDental MaterialsGentian VioletGlass Ionomer CementsHermes Composite Resinhydroxyethyl methacrylateMethacrylatesPolyestersPolyethylene GlycolsPolymethacrylic AcidsReactive Oxygen SpeciesResin Cementssilorane composite resinSilorane ResinsSiloxanesSolitaire 2 composite resinTetric ceramTetric EvoCeramtriethylene glycol dimethacrylateVitrabond

Identifiers

PMID21243381
OpenAlexW2059013457

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.