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Genotoxic potential of flowable bulk-fill composite resins (CROSBI ID 616685)

Prilog sa skupa u časopisu | sažetak izlaganja sa skupa | međunarodna recenzija

Tarle, Zrinka ; Marović, Danijela ; Tauboeck, Tobias ; Attin, Thomas ; Želježić, Davor Genotoxic potential of flowable bulk-fill composite resins // Journal of dental research. 2014. str. 106-106

Podaci o odgovornosti

Tarle, Zrinka ; Marović, Danijela ; Tauboeck, Tobias ; Attin, Thomas ; Želježić, Davor

engleski

Genotoxic potential of flowable bulk-fill composite resins

Objective: The aim of the present study was to evaluate the genotoxicity of low-viscosity bulk- fill composite resins by measuring the level of DNA strand breaks and micronucleus frequency. Methods: Three flowable bulk-fill materials [x-tra base (XB), Surefil SDR flow (SDR), Venus Bulk Fill (VB)] and one conventional flowable control composite resin [Tetric EvoFlow (TEF)] were used. Cylindrical composite specimens (diameter: 10 mm, height: 4 mm) were irradiated for 20 or 30 s with a LED curing unit at 1170 mW/cm2. The upper (0 mm) and lower specimen surface (4 mm) were mechanically scraped, and eluates were prepared for each material, surface level and curing time. Genotoxicity assessment was carried out in human peripheral blood leukocytes using the alkaline comet assay and cytokinesis-blocked micronucleus assay. Differences in values of comet assay parameters were tested by one-way ANOVA followed by Tukey post-hoc analysis, whereas chi-square test was used for the results of the micronucleus assay (α = 0.05). Results: Considering the results of the comet assay, eluates of materials polymerized for 30 s did not significantly affect the level of primary damage to DNA. When 20 s of light irradiation was applied, only TEF, at a depth of 4 mm, showed a significant increase in the percentage of DNA that migrated in the tail compared to the untreated negative control (3.6 ± 2.9 and 1.4 ± 1.7, respectively). In the micronucleus assay, none of the evaluated materials induced statistically significant formation of any of the scored chromatin abnormalities (micronuclei, nuclear buds and nucleoplasmic bridges). Conclusion: Under the experimental conditions of the present evaluation, the amount of released residual monomers in eluates used for cell culture treatment was below the critical level needed to induce biologically significant DNA damages. This study was supported by the Croatian Science Foundation.

biocompatibility ; blood ; carcinogenesis ; cell culture ; human

Sažeci sa kongresa objavljenu u tiskanm obliku.

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Podaci o prilogu

106-106.

2014.

nije evidentirano

objavljeno

Podaci o matičnoj publikaciji

Journal of dental research

0022-0345

1544-0591

Podaci o skupu

International Association for Dental Research Pan- European Region Congress 2014

poster

10.09.2014-13.09.2014

Dubrovnik, Hrvatska

Povezanost rada

Dentalna medicina

Indeksiranost