Hydrolytic stability of self-etch adhesives bonded to dentin

被引:267
作者
Inoue, S
Koshiro, K
Yoshida, Y
De Munck, J
Nagakane, K
Suzuki, K
Sano, H
Van Meerbeek, B
机构
[1] Hokkaido Univ Hosp, Ctr Dent Clin, Div Gen Dent, Kita Ku, Sapporo, Hokkaido 0608586, Japan
[2] Catholic Univ Louvain, Sch Dent, Dept Conservat Dent, Leuven BIOMAT Res Cluster, B-3000 Louvain, Belgium
[3] Hokkaido Univ, Grad Sch Dent Med, Dept Conservat Dent, Kita Ku, Sapporo, Hokkaido 0608586, Japan
[4] Okayama Univ, Grad Sch Med Dent & Pharmaceut Sci, Dept Biomat, Okayama 7008525, Japan
[5] Okayama Univ, Biomed Engn Res Ctr, Okayama 7008525, Japan
[6] Hiroshima Univ, Grad Sch Dent, Dept Biomat Sci, Minato Ku, Hiroshima 7348553, Japan
关键词
hydrolytic stability; self-etch adhesive; durability; functional monomer; dentin;
D O I
10.1177/154405910508401213
中图分类号
R78 [口腔科学];
学科分类号
1003 [口腔医学];
摘要
Functional monomers chemically interact with hydroxyapatite that remains within submicron hybrid layers produced by mild self- etch adhesives. The functional monomer 10- MDP interacts most intensively with hydroxyapatite, and its calcium salt appeared most hydrolytically stable, as compared with 4- MET and phenyl- P. We investigated the hypothesis that additional chemical interaction of self- etch adhesives improves bond stability. The micro- tensile bond strength (mu TBS) of the 10- MDP- based adhesive did not decrease significantly after 100,000 cycles, but did after 50,000 and 30,000 cycles, respectively, for the 4- MET- based and the phenyl-P- based adhesives. Likewise, the interfacial ultrastructure was unchanged after 100,000 thermocycles for the 10- MDP- based adhesive, while that of both the 4- MET- and phenyl- P- based adhesives contained voids and less- defined collagen. The findings of this study support the concept that long- term durability of adhesive-dentin bonds depends on the chemical bonding potential of the functional monomer.
引用
收藏
页码:1160 / 1164
页数:5
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