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1.
Braz. oral res. (Online) ; 32: e108, 2018. tab
Article in English | LILACS | ID: biblio-974457

ABSTRACT

Abstract This study evaluated the effect of adding the hydrophobic monomer 1,12 dodecanediol dimethacrylate (DDDMA) to experimental sealants with and without thermocycling on degree of conversion (DC), water sorption (WS), water solubility (WSB), color stability (ΔE), and micro-shear bond strength (μSBS). Five experimental and one commercially available sealant (Bisco - BIS) were tested. The experimental sealants were formulated by mixing different percentages of DDDMA monomers and urethane dimethacrylate (UDMA). The photoinitiator system was composed by camphorquinone (CQ) and tertiary amine 4-ethyl benzoate dimetilamiono (EDBA). Ethanol was used as a solvent. The experimental groups were named sequentially according to the monomeric content (DDDMA/UDMA): S40/40 (40/40), S50/30 (50/30), S60/20 (60/20), S70/10 (70/10) and S80/0 (80/0). Data were analyzed separately by one-way ANOVA, followed by Tukey's test (p<0.05). The values of DC ranged from 94.59% (S40/40) to 54.02% (S80/10). BIS showed the highest WS value (p<0.05) and S40/40, S50/30, S60/20 and S80/0 showed the lowest WS values of all tested sealants. WSB values ranged from 7.88 µg/mm3 (BIS) to 13.27 µg/mm3 (S70/10). The highest ΔE value was 11.05±2.88 for BIS and the highest μSBS value was found for S60/20. No significant difference was observed in bond strength between sealants and bovine enamel after thermocycling. Adding DDDMA to the composition of surface sealants can improve its performance, once the monomer increased the degree of conversion and the color stability.


Subject(s)
Humans , Cattle , Polymethacrylic Acids/chemistry , Polyurethanes/chemistry , Composite Resins/chemistry , Methacrylates/chemistry , Reference Values , Solubility , Surface Properties , Temperature , Time Factors , Materials Testing , Camphor/analogs & derivatives , Camphor/chemistry , Water/chemistry , Reproducibility of Results , Analysis of Variance , Dental Bonding/methods , Color , Dental Enamel/drug effects , Dental Enamel/chemistry , Shear Strength , Phase Transition , Ethanol/chemistry , Ethylenediamines/chemistry , Polymerization
2.
Braz. oral res. (Online) ; 32: e116, 2018. tab, graf
Article in English | LILACS | ID: biblio-974442

ABSTRACT

Abstract The aim of this study was to analyze the efficiency of experimental light-curing resin cements (ERCs) with a ternary photo-initiator system containing diphenyliodonium hexafluorphosphate (DPI) and different amines on retention of glass-fiber posts to dentin (GFP). ERCs formulations: a 1:1 mass ratio of 2,2-bis[4-(2-hydroxy-3-methacryloxypropoxy)phenylpropane and triethyleneglycol dimethacrylate. Camphorquinone was used as initiator. Six experimental groups were established according to the amine used: [ethyl-4-(dimethylamino)benzoate-EDMAB or 2-(dimethylamino)ethyl methacrylate-DMAEMA] and the concentration of DPI (0, 0.5 mol%, 1 mol%). The resin cements Variolink II (dual- and light-cured versions) were used as commercial reference. Eighty recently extracted bovine incisors (n = 10) were selected for this study. The roots were prepared and the fiber posts were cemented with the resin cement specified for each experimental group. Specimens from coronal, middle, and apical thirds of the root were subjected to push-out bond strength test 24 hours after bonding. Data were subjected to split-plot ANOVA and the Tukey test (p = 0.05). ERCs containing DPI showed statistically significant higher bond strengths compared with ERCs without DPI. ERCs containing DPI were statistically similar to VARIOLINK II - dual-cured and superior to VARIOLINK II - light-cured (except for EDMAB - 1DPI in the medium third and DMAEMA - 1DPI in the coronal third). Different amines did not influence post retention. The apical root region showed the lowest bond strength for the groups EDAB-0DPI, DMAEMA-0DPI and VARIOLINK II light-cured. Light-cured ERCs containing DPI were efficient for GFP retention to radicular dentin, with similar behaviour to that of dual-curing commercial resin cement.


Subject(s)
Onium Compounds/chemistry , Biphenyl Compounds/chemistry , Post and Core Technique , Tooth Apex/drug effects , Resin Cements/chemistry , Dentin/drug effects , Light-Curing of Dental Adhesives/methods , Photoinitiators, Dental/chemistry , Onium Compounds/radiation effects , Time Factors , Tooth Fractures , Biphenyl Compounds/radiation effects , Materials Testing , Analysis of Variance , Tooth Apex/radiation effects , Resin Cements/radiation effects , Dentin/radiation effects , Curing Lights, Dental , Photoinitiators, Dental/radiation effects , Polymerization , para-Aminobenzoates/radiation effects , para-Aminobenzoates/chemistry , Glass/radiation effects , Glass/chemistry , Methacrylates/radiation effects , Methacrylates/chemistry
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