Elution of TEGDMA and HEMA from polymerized resin-based bonding systems

Objectives s study the amount of TEGDMA and HEMA eluted from several adhesive systems was quantified. s hesive systems were applied according to manufacturers’ instructions in an analytic vial. The adhesive systems used were (abbreviation and producer in parenthesis): cmf adhesive system® (CMF) (Saremco), ENAbond (EB) (Micerium), Optibond FL (OB) (Kerr), Adper Scotchbond Multi-Purpose (SB) (3M ESPE), Silorane System Adhesive (SSA) (3M ESPE), Syntac Classic (SC) (Ivoclar Vivadent) and XP Bond (XPB) (Dentsply). After preparation the specimens were immersed in methanol or distilled water for a period from 1 d to 30 d at 37 °C. Eluted TEGDMA and HEMA were determined by gas chromatographic–mass spectrometry (GC–MS). s ing TEGDMA elution from adhesives was found (μg/ml; mean and standard deviation(sd); 1 d/30 d; methanol): SC 0.93(0.8)/0.68(0.5), SSA 0.27(0.09)/0.16(0.04) and XPB 0.25(0.1)/0.19(0.09). TEGDMA eluted from EB, CMF, OB, and SB was always below detection limit. TEGDMA water elution from each adhesive was about 1/5 lower, compared to the corresponding TEGDMA methanol elution. ing HEMA elution was found (μg/ml; mean(sd); 1 d/30 d; methanol): SB 3.42(0.9)/2.02(1.2), EB 3.07(2.2)/2.15(2.2), XPB 2.47(1.6)/1.89(1.1), OB 1.4(0.7)/0.82(0.2) and SSA 0.44(0.2)/0.17(0.07). HEMA eluted from CMF and SC was always below detection limit. HEMA water elution from each adhesive was about 1/10 lower, compared to the corresponding HEMA methanol elution. icance A, and XPB eluted TEGDMA. SB, EB, XPB, OB, and SSA eluted HEMA. CMF eluted neither HEMA nor TEGDMA.