AI Article Synopsis

  • The study evaluated the effects of varying concentrations of ZnCl in adhesive systems on factors like degree of conversion, water sorption, solubility, and bonding stability with dentin.
  • Zn0 (control), Zn2 (2%), Zn3.5 (3.5%), and Zn5 (5%) were tested, with Zn5 showing the lowest degree of conversion and highest water sorption and solubility.
  • Results indicated that 2 wt.% ZnCl enhanced bonding stability after 12 months, while higher concentrations negatively affected physicochemical properties.

Article Abstract

The aim of this study was to evaluate the degree of conversion (DC%), water sorption (WS), solubility (SO), and resin-dentin bonding stability of experimental adhesive systems containing ZnCl. Different concentrations (wt.%) of ZnCl were added to a model etch-and-rinse adhesive system consisting of BISGMA, HEMA, UDMA, GDMA, water, and ethanol: Zn0 (0%-control group); Zn2 (2%); Zn3.5 (3.5%); and Zn5 (5%). Adper Single Bond 2 (SB) was used as commercial reference. The samples were light cured for 20s using a quartz-tungsten-halogen unit (650 mW/cm). DC% ( = 5) was measured using FT-IR spectroscopy, and WS and SO ( = 5) were calculated based on ISO4049. Microtensile bond strength (TBS) and nanoleakage (NL) were measured after 24 h and 12 months of water storage ( = 10). Data were analyzed using ANOVA and Tukey's HSD test (5%). Zn5 presented the lowest DC% and the highest WS and SO ( < 0.05). Zn0 and Zn2 presented statistically similar DC%, WS, SO, and immediate TBS. All adhesives containing ZnCl maintained a TBS stability after 12 months, but only Zn2 and Zn3.5 did not suffer an increase in NL. SB presented the highest immediate TBS but the greatest reduction after 12 months ( < 0.05). The addition of 2 wt.% of ZnCl in adhesive formulations seems to be a promising way to improve the resin-dentin bonding stability. Higher concentrations than 2 wt.% could impair some physicochemical properties.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5706081PMC
http://dx.doi.org/10.1155/2017/5940479DOI Listing

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