Nihon University Graduate School of Dentistry at Matsudo, Crown Bridge Prosthodontics, Chiba 271-8587, Japan; Department of Crown Bridge Prosthodontics, Nihon University School of Dentistry at Matsudo, Chiba 271-8587, Japan.
Department of Biomedical Engineering, Iwate Medical University, Iwate 028-3694, Japan.
Dent Mater. 2017 Dec;33(12):1371-1380. doi: 10.1016/j.dental.2017.09.001. Epub 2017 Oct 16.
Bonding to zirconia has been of great interest over the last 10-15 years. The aim of this study was to develop a zirconia bonding system and clarify its adhesion mechanism.
A zirconia primer was prepared using tetra-n-propoxy zirconium (TPZr) and water. A silane primer was also prepared using γ-methacryloyloxypropyltrimethoxysilane (γ-MPS) and hydrochloric acid. After the zirconia primer was applied to the oxidized zirconia surface, the silane primer was applied to the ZrO-functionalized layer and the resin cement was applied to the silane-modified layer. Ceramic Primer II was used as a typical MDP-based ceramic primer. Shear bond strengths were measured using a universal testing machine. To clarify the enhancing mechanism of the zirconia bonding system, X-ray photoelectron spectroscopy (XPS) analyses were performed.
The zirconia bond strength was affected by the surface wettability of zirconia, and the compositions of TPZr and water utilized in the zirconia primer. When the zirconia primer, consisting of 10μL TPZr and 13μL water, was applied to the zirconia surface that had been oxidized by HO above 10%, the maximum bond strength of 8.2MPa was obtained. The mechanism of the zirconia bonding system was established as follows: the hydrolyzed zirconium species formed a more reactive ZrO-functionalized layer on the oxidized zirconia surface, and the hydrolyzed γ-MPS species adsorbed on that layer introduces a chemical bonding to the resin.
The novel zirconia bonding system enhanced the bonding performance of the resin, and showed a greater bond strength than an MDP-based ceramic primer.
在过去的 10-15 年中,氧化锆的粘结性能一直备受关注。本研究旨在开发一种氧化锆粘结系统并阐明其粘结机制。
采用四正丙氧基锆(TPZr)和水制备氧化锆底涂剂。采用γ-甲基丙烯酰氧基丙基三甲氧基硅烷(γ-MPS)和盐酸制备硅烷底涂剂。将氧化锆底涂剂涂覆于氧化锆表面后,将硅烷底涂剂涂覆于 ZrO 功能化层,再将树脂水门汀涂覆于硅烷改性层。陶瓷底涂剂 II 用作典型的基于 MDP 的陶瓷底涂剂。采用万能试验机测量剪切粘结强度。为了阐明氧化锆粘结系统的增强机制,进行了 X 射线光电子能谱(XPS)分析。
氧化锆粘结强度受氧化锆表面润湿性的影响,以及氧化锆底涂剂中 TPZr 和水的组成影响。当将由 10μL TPZr 和 13μL 水组成的氧化锆底涂剂涂覆于氧化锆表面,氧化锆表面经 HO 氧化超过 10%时,获得最大的 8.2MPa 粘结强度。氧化锆粘结系统的机理如下:水解的锆物种在氧化锆表面形成更具反应性的 ZrO 功能化层,水解的γ-MPS 物种吸附在该层上,从而与树脂形成化学键。
新型氧化锆粘结系统提高了树脂的粘结性能,表现出比基于 MDP 的陶瓷底涂剂更高的粘结强度。