Cytotoxicity of contemporary resin-based dental materials in contact with dentin.
Autor: | Carrillo-Cotto R; Department of Restorative Dentistry and Dental Biomaterials, School of Dentistry, University of San Carlos of Guatemala, Guatemala city, Guatemala.; Graduate Program in Dentistry, Federal University of Pelotas, Pelotas, Brazil., Etges A; Graduate Program in Dentistry, Federal University of Pelotas, Pelotas, Brazil., Jardim PS; Private Dental Office, Pelotas, Brazil., Torre E; Graduate Program in Dentistry, Federal University of Pelotas, Pelotas, Brazil., Kaizer MR; Graduate Program in Dentistry, Positivo University, Curitiba, Brazil., Ferrúa CP; Graduate Program in Health and Behavior, Catholic University of Pelotas, Pelotas, Brazil., Nedel F; Graduate Program in Health and Behavior, Catholic University of Pelotas, Pelotas, Brazil., Cuevas-Suárez CE; Dental Materials Laboratory, Autonomous University of Hidalgo State, Pachuca, Mexico., Moraes RR; Graduate Program in Dentistry, Federal University of Pelotas, Pelotas, Brazil. |
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Jazyk: | angličtina |
Zdroj: | European journal of oral sciences [Eur J Oral Sci] 2020 Oct; Vol. 128 (5), pp. 436-443. Date of Electronic Publication: 2020 Aug 02. |
DOI: | 10.1111/eos.12723 |
Abstrakt: | In this study, the cytotoxicity of different combinations of contemporary resin-based restoratives (adhesives, composites, luting agents) against human keratinocytes (HaCaT) was evaluated under two conditions, whether materials were applied to dentin or not. Adhesives (3-step etch-and-rinse/3ER: OptiBond FL; 2-step self-etch/2SE Clearfil SE Bond; Single Bond Universal/UNI), composites (conventional composite resin/CCR: Filtek Z350XT; flowable/FCR: Filtek Z350XT Flow; self-adhesive composite resin/SACR: Dyad Flow), and luting agents (conventional luting agent/CLA: Variolink-II; self-adhesive luting agent/SLA: RelyXU200) were combined according to their clinical use. Eluates from polymerized specimens applied to dentin were placed in contact with cells grown for 1 and 7 d. The controls were defined by cells without material contact. Cell viability was determined using MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide)] assay. C=C conversion was investigated using Fourier-transform infrared spectroscopy. After 1 d of incubation, when dentin was not present, 2SE yielded the highest cell viability, whereas 3ER, UNI, and SACR showed higher cell viability in the presence of dentin. After 7 d, when dentin was absent, 2SE and CLA achieved significantly higher cell viability. The presence of dentin resulted in a drastically higher cell viability for all materials, except 2SE and CLA. UNI had the lowest C=C conversion. The presence of dentin was a significant factor, which resulted in higher cell viability than what was seen for the material specimens per se. All materials resulted in a lower viability of HaCaT than what was seen under the no-material control conditions, with effects mainly limited to the first 24 h. (© 2020 Eur J Oral Sci.) |
Databáze: | MEDLINE |
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