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Original Articles

A new experimental adhesive system containing G-IEMA – physicochemical properties

, , ORCID Icon & ORCID Icon
Pages 418-432 | Received 24 Apr 2018, Accepted 13 Oct 2018, Published online: 09 Dec 2018
 

Abstract

The ultimate goal of this study was the development of a new Bis-GMA-free dental adhesive system with improved adhesive properties. Instead of Bis-GMA, a dendritic macromer (G-IEMA), derived from 2-isocyanatoethyl methacrylate (IEMA), was used and its physicochemical properties were investigated. G-IEMA was synthesized and subsequently incorporated into an experimental adhesive (AE2) formulated without Bis-GMA. Double bond conversion (DBC), polymerization shrinkage (PS), water sorption (WS) and solubility (SL) were evaluated and results were compared with three other adhesives: – an experimental adhesive formulated with Bis-GMA (AE1); Scotchbond™ (SBU); and, Futurabond M+ (FUT). Comparisons between adhesives for DBC, PS, WS and SL properties were performed using One-Way ANOVA and the Kruskal-Wallis test, at the 5% significance level. Statistical analysis of DBC data, using one-way ANOVA, revealed significant differences between adhesives (p < .001). AE2 presented a significantly higher DBC than SBU (p < .001) and FUT (p = .004); no significant differences were observed between AE2 and AE1 (p = .403) with 60 s of light-curing. Kruskal-Wallis test revealed no significant differences between adhesives (p = .094) for PS. One-Way ANOVA showed no significant differences among adhesives for WS (p = .213) and SL (p = .175). In conclusion, G-IEMA-based adhesive AE2 presented comparable DBC, PS, WS and SL when compared to Bis-GMA-based adhesive AE1. The results obtained so far are promising, revealing that G-IEMA macromer might be a good substitute monomer to prepare Bis-GMA-free adhesive systems.

Acknowledgments

The authors are grateful to VOCO GmbH (Cuxhaven, Germany) for providing Futurabond M+ used in the present study. Moreover, the NMR spectrometer used in this work are part of the national NMR Facility, supported by Fundação para a Ciência e Tecnologia (RECI/BBB-BQB/0230/2012).

Disclosure statement

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.

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