PubMed · 14959869
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Robert Saxe. 2004. Light-curing times.. https://doi.org/10.14219/jada.archive.2004.0004
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The aim of this study was to test the ability of an infrared (IR) camera to assess temperature changes and distributions in teeth below restorations when quartz-tungsten-halogen (QTH) and light-emitting diode (LED) curing lights were used to photopolymerize the restorative material. Our hypothesis was that the higher power density and broader spectral distribution of the QTH source would cause greater increases in tooth temperature than the LED source, and that these differences would be best demonstrated with the IR camera. Cavities were prepared on human third molars and restored with a resin composite restorative material. The material was light-cured using three light-curing sources using several exposure times. The external (outside the tooth) and internal (inside the pulp chamber) temperature changes during polymerization of the composite material were recorded over 360 s with thermocouples and an IR camera. Using thermocouples the maximum increase in external temperature (+17.7 degrees C) was reported for the Swiss Master light after 20 s of curing time while the minimum temperature rise (+7.8 degrees C) was reported for the Freelight 2. Whereas a 2.6 degrees C increase in internal temperature was observed after curing 20 s with the Freelight 2, 7.1 degrees C was reported after 60 s of light exposure to Astralis 10. Infrared images showed similar trends in external-internal rises in temperature as the thermocouples, although temperatures measured by the IR were generally higher. These results indicate that the higher power density QTH sources caused greater increases in tooth temperatures than the LED source and that thermocouples may underestimate the heat applied to the tooth.
This research aimed to determine the elastic modulus of resin-based dental composite restoratives using the microindentation test method. Results were then compared with those obtained with the ISO three-point bending test method. Five materials from the same manufacturer (3M ESPE) were selected for the study. They included microfill (A110), minifill (Z100 and Filtek Z250), poly-acid modified (F2000), and flowable (Filtek Flowable [FF]) composites. The indentation moduli of the composites were determined using a custom-designed microindentation test set up after conditioning in water at 37 degrees C for 1 week and 1 month. The indentation test was carried out at peak load of 10 N and Oliver & Pharr's method was used to determine the maximum projected contact area. Data was analyzed using ANOVA/post-hoc Scheffe's test at significance level 0.05 and Pearson's correlation at significance level 0.01. The mean indentation modulus ranged from 5.80 to 15.64 GPa and 5.71 to 15.35 GPa at 1 week and 1 month, respectively. At both time periods, the indentation modulus of Z100 was significantly higher than all other materials. F2000 was significantly higher than Z250, which was significantly stiffer than A110 and FF. The rankings were in good agreement with the ISO flexural test. A significant, positive, and strong correlation (r = 0.93 and 0.94 at 1 week and 1 month, respectively) in modulus between ISO three-point bending and microindentation test methods was observed. In view of the small specimen size and good reproducibility, the microindentation reflects a potential test method for determining the elastic properties of dental composite restoratives.
Hydroxyl radical (*OH)-induced inflammation is a primary mode for in vivo cytotoxicity. A legitimate concern is whether particulate wear debris from orthopedic composites can stimulate inflammation via ferrous ion (Fe2+)-mediated production of *OH. The purpose of this research was to utilize electron paramagnetic resonance (EPR) spin trapping in investigating and comparing the potential for postsurgical cytotoxicity induced specifically by *OH in the presence of two composites: Simplex P and the novel, hybrid, CORTOSS. Cytotoxicity is evaluated based on the composites competitively chelating catalytic Fe2+ or readily reducing ferric ions (Fe3+), in facilitating the Fenton reaction (FR). *OH that are produced were then validated by a radical scavenger to confirm a genuine radical signal and mechanism. Spin adduct peak areas decreased in the presence of CORTOSS as opposed to increasing in the presence of Simplex P, evaluated against their respective controls. A plausible theory elucidating this finding is that CORTOSS may sequester the Fe form, by virtue of its monomers. Principally, direct comparison of composites indicated that Simplex P had greater tendency to produce *OH, yielding 25.6 and 48.7% greater spin adduct peak areas when chelated and non-chelated Fe2+ are used, respectively. Moreover, the rate of FR accelerated when chelated Fe2+ was used, leading to the formation of a ternary complex with the composites. This was more prominent in Simplex P, as coordination of chelated Fe2+ occurs on its surface via an electrostatic attraction to allow a seventh coordination site for ligand exchange in the ternary complex, stabilized by Ba2+. Conversely, the silica found in CORTOSS possesses radical quenching abilities that deactivate generated *OH in impeding the efficiency of FR. Neither composite demonstrated a capacity to readily reduce Fe3+ to the relevant Fe2+, as validated by a non-radical pathway. Instead, the artificial spin adduct signal attained when employing chelated Fe3+ was due to the nucleophilic addition of water onto DMPO. Simplex P may also serve as a template for surface catalysis of the nucleophilic addition of water onto DMPO involving chelated Fe3+. CORTOSS is thought not to induce cytotoxicity, whereas the propensity of Simplex P in promoting Fenton chemistry is a serious issue that must be addressed.