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Cytotoxicity of flowable resin composite on cultured human periodontal ligament cells compared with mineral trioxide aggregate.
- Source :
-
Journal of investigative and clinical dentistry [J Investig Clin Dent] 2012 Aug; Vol. 3 (3), pp. 215-20. Date of Electronic Publication: 2012 Apr 30. - Publication Year :
- 2012
-
Abstract
- Aim: To investigate the cytotoxicity of three flowable resin composites that potentially useful as retrograde filling materials, compared with mineral trioxide aggregate (MTA).<br />Methods: Ten standard cylinder discs were used for each of the tested materials: Tetric Flow, Filtex Flow, Aeliteflo, and MTA, which were prepared under aseptic conditions. Cytotoxicity of eluates from all materials after 1-4 days' immersion in culture medium and direct contact cytotoxicity were evaluated using cultured human periodontal ligament cells (PDLC). The colorimetric (3-[4,5-dimethylthiazol-2-yl]-2,5-diphenyltetrazolium bromide) assay and scanning electron microscope of cell morphology (direct contact only) were used.<br />Results: No eluates of set materials demonstrated cytotoxicity at any concentration or elution time. Freshly-mixed MTA was cytotoxic in direct contact, but not set MTA. Freshly-mixed Aeliteflo was also cytotoxic, as was set material up to 2 days' elution. With morphological assessment, some differences were seen among resin composites, but all changes were rated as slight using the International Standard Organization criteria.<br />Conclusions: Of all of the materials tested, Tetric Flow showed the least cytotoxic effects on PDLC. Further research is needed to determine the clinical usefulness of flowable composites as retrograde filling materials.<br /> (© 2012 Blackwell Publishing Asia Pty Ltd.)
Details
- Language :
- English
- ISSN :
- 2041-1626
- Volume :
- 3
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Journal of investigative and clinical dentistry
- Publication Type :
- Academic Journal
- Accession number :
- 22544568
- Full Text :
- https://doi.org/10.1111/j.2041-1626.2012.00125.x