کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
3145762 | 1197102 | 2006 | 7 صفحه PDF | دانلود رایگان |

ObjectivesThree activated organofunctional silane coupling agents alone and blended with a non-functional cross-linker silane were evaluated as adhesion promoters in an experiment where a bis-GMA (bis-phenol-A-diglycidyldimethacrylate) resin was bonded to silicatized titanium. The adhesive performances of the silanes were assessed as shear bond strength values.Materials and methods3-Methacryloyloxypropyltrimethoxysilane, N-[3-(trimethoxysilyl)propyl]ethylenediamine and [3-(triethoxysilyl)propyl]urea were prepared as 1.0 vol.% solutions in 95 vol.% ethanol. They were each also blended with 1.0 vol.% 1,2-bis-(triethoxysilyl)ethane solutions that were activated for 1 or 24 h. Titanium slides were cleaned, silicatized, distributed randomly to study groups and silanized with nine silane solutions. After silanization experimental bis-GMA resin stubs were photo-polymerized and post-polymerized in a light-curing unit. The shear bond strength was measured as ‘dry samples’ and after thermo-cycling (6000 cycles at 5–55 °C).ResultsThe type of silane affected significantly the shear bond strength (p < 0.001) and the use of cross-linker silane (p < 0.005) according to the statistical analysis (ANOVA). It showed that the highest shear bond strength for thermo-cycled resin stub samples (n = 8/group) was obtained with a blend of 1.0 vol.% 3-methacryloyloxypropyltrimethoxysilane + 1.0 vol.% 1,2-bis-(triethoxysilyl)ethane blend (10.4 ± 3.5 MPa). The lowest results were obtained with 1.0 vol.% [3-(triethoxysilyl)propyl]urea (4.5 ± 1.0 MPa), and with 1.0 vol.% N-[3-(trimethoxysilyl)propyl]ethylenediamine (4.5 ± 1.4 MPa).ConclusionsSilanization with a blend of a functional silane and a cross-linker silane (a novel silane system) might improve the hydrolytic stability of a siloxane film between silicatized titanium and a bis-GMA resin.
Journal: Journal of Dentistry - Volume 34, Issue 10, November 2006, Pages 740–746