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Influence of light-curing mode on the cytotoxicity of resin-based surface sealants

BACKGROUND: Surface sealants have been successfully used in the prevention of erosive tooth wear. However, when multiple tooth surfaces should be sealed, the light-curing procedure is very time-consuming. Therefore, the aim of this study was to investigate whether reduced light-curing time (while ma...

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Autores principales: Wegehaupt, Florian J, Tauböck, Tobias T, Attin, Thomas, Belibasakis, Georgios N
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4019812/
https://www.ncbi.nlm.nih.gov/pubmed/24885810
http://dx.doi.org/10.1186/1472-6831-14-48
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author Wegehaupt, Florian J
Tauböck, Tobias T
Attin, Thomas
Belibasakis, Georgios N
author_facet Wegehaupt, Florian J
Tauböck, Tobias T
Attin, Thomas
Belibasakis, Georgios N
author_sort Wegehaupt, Florian J
collection PubMed
description BACKGROUND: Surface sealants have been successfully used in the prevention of erosive tooth wear. However, when multiple tooth surfaces should be sealed, the light-curing procedure is very time-consuming. Therefore, the aim of this study was to investigate whether reduced light-curing time (while maintaining similar energy density) has an influence on resin-based surface sealant cytotoxicity. METHODS: Bovine dentine discs were treated as follows: group 1: untreated, groups 2–5: Seal&Protect and groups 6–9: experimental sealer. Groups 2 and 6 were light-cured (VALO LED light-curing device) for 40 s (1000 mW/cm(2)), groups 3 and 7 for 10 s (1000 mW/cm(2)), groups 4 and 8 for 7 s (1400 mW/cm(2)) and groups 5 and 9 for 3 s (3200 mW/cm(2)). Later, materials were extracted in culture medium for 24 h, and released lactate dehydrogenase (LDH) activity as a measure of cytotoxicity was determined photometrically after cells (dental pulp cells and gingival fibroblasts) were exposed to the extracts for 24 h. Three independent experiments, for both sample preparation and cytotoxicity testing, were performed. RESULTS: Overall, lowest cytotoxicity was observed for the unsealed control group. No significant influence of light-curing settings on the cytotoxicity was observed (p = 0.537 and 0.838 for pulp cells and gingival fibroblasts, respectively). No significant difference in the cytotoxicity of the two sealants was observed after light-curing with same light-curing settings (group 2 vs. 6, 3 vs. 7, 4 vs. 8 and 5 vs. 9: p > 0.05, respectively). CONCLUSIONS: Shortening the light-curing time, while maintaining constant energy density, resulted in no higher cytotoxicity of the investigated sealants.
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spelling pubmed-40198122014-05-15 Influence of light-curing mode on the cytotoxicity of resin-based surface sealants Wegehaupt, Florian J Tauböck, Tobias T Attin, Thomas Belibasakis, Georgios N BMC Oral Health Research Article BACKGROUND: Surface sealants have been successfully used in the prevention of erosive tooth wear. However, when multiple tooth surfaces should be sealed, the light-curing procedure is very time-consuming. Therefore, the aim of this study was to investigate whether reduced light-curing time (while maintaining similar energy density) has an influence on resin-based surface sealant cytotoxicity. METHODS: Bovine dentine discs were treated as follows: group 1: untreated, groups 2–5: Seal&Protect and groups 6–9: experimental sealer. Groups 2 and 6 were light-cured (VALO LED light-curing device) for 40 s (1000 mW/cm(2)), groups 3 and 7 for 10 s (1000 mW/cm(2)), groups 4 and 8 for 7 s (1400 mW/cm(2)) and groups 5 and 9 for 3 s (3200 mW/cm(2)). Later, materials were extracted in culture medium for 24 h, and released lactate dehydrogenase (LDH) activity as a measure of cytotoxicity was determined photometrically after cells (dental pulp cells and gingival fibroblasts) were exposed to the extracts for 24 h. Three independent experiments, for both sample preparation and cytotoxicity testing, were performed. RESULTS: Overall, lowest cytotoxicity was observed for the unsealed control group. No significant influence of light-curing settings on the cytotoxicity was observed (p = 0.537 and 0.838 for pulp cells and gingival fibroblasts, respectively). No significant difference in the cytotoxicity of the two sealants was observed after light-curing with same light-curing settings (group 2 vs. 6, 3 vs. 7, 4 vs. 8 and 5 vs. 9: p > 0.05, respectively). CONCLUSIONS: Shortening the light-curing time, while maintaining constant energy density, resulted in no higher cytotoxicity of the investigated sealants. BioMed Central 2014-05-06 /pmc/articles/PMC4019812/ /pubmed/24885810 http://dx.doi.org/10.1186/1472-6831-14-48 Text en Copyright © 2014 Wegehaupt et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Wegehaupt, Florian J
Tauböck, Tobias T
Attin, Thomas
Belibasakis, Georgios N
Influence of light-curing mode on the cytotoxicity of resin-based surface sealants
title Influence of light-curing mode on the cytotoxicity of resin-based surface sealants
title_full Influence of light-curing mode on the cytotoxicity of resin-based surface sealants
title_fullStr Influence of light-curing mode on the cytotoxicity of resin-based surface sealants
title_full_unstemmed Influence of light-curing mode on the cytotoxicity of resin-based surface sealants
title_short Influence of light-curing mode on the cytotoxicity of resin-based surface sealants
title_sort influence of light-curing mode on the cytotoxicity of resin-based surface sealants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4019812/
https://www.ncbi.nlm.nih.gov/pubmed/24885810
http://dx.doi.org/10.1186/1472-6831-14-48
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