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复合树脂-牙本质粘结剂界面的触变聚合。

Touch-Cure Polymerization at the Composite Cement-Dentin Interface.

机构信息

National Institute of Advanced Industrial Science and Technology (AIST), Health and Medical Research Institute, Takamatsu, Kagawa, Japan.

Okayama University, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Department of Pathology & Experimental Medicine, Okayama, Japan.

出版信息

J Dent Res. 2021 Aug;100(9):935-942. doi: 10.1177/00220345211001020. Epub 2021 Mar 26.

Abstract

Ceramic restorations are often adhesively luted onto the tooth prep. The so-called touch-cure concept was developed to yield optimum polymerization of composite cement at the restoration-cement-tooth interface for immediate bond stabilization. Although this touch cure is theorized to initiate polymerization at the interface when the accelerator in the primer makes contact with the cement, this process has not yet been proven. This study aimed to elucidate the mechanism of touch cure by measuring the degree of conversion (DC) of composite cement applied with or without an accelerator-containing tooth primer (TP) versus an accelerator-free primer using real-time Fourier-transform infrared spectroscopy (RT-FTIR) and attenuated total reflection (ATR)-FTIR. Interfacial bond strength was measured in shear mode, the accelerator composition confirmed by X-ray fluorescence analysis (XRF), and the interfacial interaction of TP and composite cement with dentin investigated by X-ray diffraction (XRD), focused-ion-beam scanning electron microscopy (FIB-SEM) with 3-dimensional interface reconstruction, and transmission electron microscopy (TEM). RT/ATR-FTIR revealed the significantly highest DC when the composite cement was applied with the accelerator-containing primer. XRF disclosed a vanadium compound as a novel chemical accelerator within TP, instead of a classic chemical curing initiator system, to set off touch cure as soon the cement contacts the previously applied primer. Although the TP contains the acidic functional monomer 10-MDP for adhesion to tooth tissue, touch cure using the accelerator-containing TP combined the fastest/highest DC with the highest bond strength. FIB-SEM and TEM confirmed the tight interfacial interaction at dentin with submicron hybridization along with stable 10-MDP also Ca-salt nanolayering.

摘要

陶瓷修复体通常通过黏接剂黏附在牙体预备体上。所谓的触变固化理念是为了在修复体-黏结剂-牙体界面实现最佳的复合树脂聚合,从而实现即刻黏结稳定。虽然理论上认为当底漆中的促进剂与黏结剂接触时,会在界面引发聚合,但这一过程尚未得到证实。本研究旨在通过实时傅里叶变换红外光谱(RT-FTIR)和衰减全反射(ATR)-FTIR 测量含促进剂的牙底漆(TP)和无促进剂的底漆涂覆的复合树脂的转化率(DC),来阐明触变固化的机制。采用剪切模式测量界面结合强度,通过 X 射线荧光分析(XRF)确认促进剂的组成,并通过 X 射线衍射(XRD)、聚焦离子束扫描电子显微镜(FIB-SEM)与三维界面重建以及透射电子显微镜(TEM)研究 TP 和复合树脂与牙本质的界面相互作用。RT/ATR-FTIR 结果表明,当复合树脂与含促进剂的底漆一起使用时,转化率最高。XRF 显示,TP 中含有一种新型化学促进剂钒化合物,而不是经典的化学固化引发剂体系,可在黏结剂接触到先前应用的底漆时引发触变固化。虽然 TP 含有用于黏附牙体组织的酸性官能单体 10-MDP,但使用含促进剂的 TP 进行触变固化可实现最快/最高的 DC 和最高的结合强度。FIB-SEM 和 TEM 证实,在牙本质上存在紧密的界面相互作用,亚微米级的杂交与稳定的 10-MDP 以及 Ca 盐纳米层共存。

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