能与牙本质进行双重化学结合的新型单体,可提高粘接耐久性。

Journal of dental research Pub Date : 2024-07-01 Epub Date: 2024-06-13 DOI:10.1177/00220345241253526
H M Wang, K X Li, Z L Tian, Y L Zhu, X Y Liu, S H Yang, S W Qiao, S Zhu, Z S Shi
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引用次数: 0

摘要

牙本质粘接微环境富含水分,再加上粘接界面上的应力,会导致混合层水解降解,导致粘接耐久性下降,最终导致修复失败。目前,三步蚀刻-冲洗技术仍是牙本质粘接的黄金标准,其粘接机制主要涉及物理相互作用,很少涉及化学粘接。在这项研究中,我们开发了一种硅氧烷改性聚氨酯单体(SPU),它具有丙烯酸酯和硅氧烷改性,能与牙本质中的胶原蛋白和羟基磷灰石发生化学结合。作为双酚 A-甲基丙烯酸缩水甘油酯的替代品,这种基于 SPU 单体的粘合剂旨在提高牙本质粘合质量和耐久性。在 SPU 处理过的胶原、羟基磷灰石和酸蚀牙本质切片上进行了衰减全反射傅立叶变换红外光谱、热重分析、X 射线光电子能谱、扫描电子显微镜、透射电子显微镜和羟脯氨酸释放测定。对配置好的 SPU 粘合剂的物理化学特性进行了分析,包括聚合行为、水接触角、拉伸应变和强度。通过对热循环老化前后的粘合样本进行显微拉伸强度和纳米渗漏测试,评估了粘合效果。最后,我们进一步进行了体内和体外实验,以评估粘合剂的生物相容性。结果表明,SPU 单体的硅氧烷基团可与牙本质胶原和羟基磷灰石共价结合。在粘合剂中加入 SPU 后,粘合剂的聚合度显著提高(P < 0.05),断裂拉伸应变高达 134.11%。此外,SPU 粘合剂明显提高了牙本质粘接强度(P < 0.05),减少了界面纳米渗漏(P < 0.05),并显示出良好的生物相容性。总之,SPU 能与牙本质实现双重化学结合,可以提高混合层的质量,缓冲界面应力,增强界面抗水解性,为延长粘接修复体的使用寿命提供了一种可行的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New Monomer Capable of Dual Chemical Binding with Dentin to Improve Bonding Durability.

The water-rich nature of the dentin bonding microenvironment, coupled with the stresses on the bonding interface, contributes to the hydrolytic degradation of the hybrid layer, resulting in a decline in bonding durability and, ultimately, restoration failure. Currently, the 3-step etch-and-rinse technique remains the gold standard for dentin bonding, and the bonding mechanism mainly involves a physical interaction with little chemical bonding. In this study, we have developed a siloxane-modified polyurethane monomer (SPU) with acrylate and siloxane modifications that chemically binds to both collagen and hydroxyapatite in dentin. Formulated as a bisphenol A-glycidyl methacrylate alternative, the SPU monomer-based adhesive was designed to improve dentin bonding quality and durability. Attenuated total reflection Fourier transform infrared spectroscopy, thermogravimetric analysis, X-ray photoelectron spectroscopy, scanning electron microscopy, transmission electron microscope, and hydroxyproline release assays were performed on SPU-treated collagen, hydroxyapatite, and acid-etched dentin slices to dentin. The physicochemical properties of the configured SPU adhesives were profiled for polymerization behavior, water contact angle, and tensile strain and strength. The bonding effectiveness was assessed through micro-tensile strength, nano-leakage tests conducted on the bonded samples before and after thermal cycle aging. Finally, we further conducted in vivo and in vitro experiments to assess the biocompatibility of adhesives. The results showed that the siloxane groups of SPU monomer could covalently bind to dentin collagen and hydroxyapatite. The incorporation of SPU in the adhesive led to a significant increase in adhesive polymerization (P < 0.05) and tensile strain at break up to 134.11%. Furthermore, the SPU adhesive significantly improved dentin bond strength (P < 0.05), reduced interfacial nano-leakage (P < 0.05), and displayed good biocompatibility. In conclusion, the application of SPU, which achieves dual chemical bonding with dentin, can improve the quality of the hybrid layer, buffer the interfacial stresses, enhance the interfacial resistance to hydrolysis, and provide a feasible strategy to extend the service life of adhesive restorations.

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