TY - JOUR
T1 - A new experimental adhesive system containing G-IEMA–physicochemical properties
AU - Vasconcelos e Cruz, Joana
AU - Brito, José
AU - Polido, Mário
AU - Gonçalves, Luísa L.
N1 - Publisher Copyright:
© 2018, © 2018 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2019/2/16
Y1 - 2019/2/16
N2 - 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.
AB - 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.
KW - Bis-GMA-free dental adhesives
KW - Dental adhesives
KW - G-IEMA
KW - dendrimers
KW - one-bottle dental adhesives
KW - physicochemical properties
UR - http://www.scopus.com/inward/record.url?scp=85058150985&partnerID=8YFLogxK
U2 - 10.1080/01694243.2018.1539154
DO - 10.1080/01694243.2018.1539154
M3 - Article
AN - SCOPUS:85058150985
SN - 0169-4243
VL - 33
SP - 418
EP - 432
JO - Journal of Adhesion Science and Technology
JF - Journal of Adhesion Science and Technology
IS - 4
ER -