University of Missouri-Kansas City School of Dentistry, Kansas City, MO, USA.
J Dent Res. 2021 Oct;100(11):1251-1257. doi: 10.1177/00220345211007428. Epub 2021 Apr 24.
Current adhesives bond to dentin via a micro-interlocking mechanism within the hybrid layer. Besides such mechanical retention, bonding to dentin would benefit from additional chemical interaction between collagen and resin. This study aims to synthesize a novel light-curable collagen crosslinker methacrylate (MA) functionalized grapeseed extract (GSE) and to assess MAGSE's ability to crosslink dentin collagen in a clinically relevant setting as well as its role in light-cure as a resin. MA functionalization was accomplished by reacting GSE with methacryloyl chloride to obtain MAGSE, which was characterized by H-NMR and Fourier transformed infrared spectroscopy (FTIR). The 6-µm-thick dentin films were microtomed from dentin slabs of third molars. Following demineralization, they were treated for 30 s by 1% MAGSE. Collagen crosslinking and resistance to digestion of MAGSE were evaluated by FTIR, matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF) assay of films, and scanning electron microscopy (SEM)/transmission electron microscopy (TEM) on slabs. Meanwhile, 1% MAGSE or GSE was added to an experimental adhesive formulated with 2-hydroxyethyl methacrylate and a tricomponent photoinitiator system. Polymerization kinetics were monitored continuously in real time for 10 min using FTIR-attenuated total reflection. The results indicated that MAGSE could bind to dentin collagen and protect it from collagenase degradation as strong as GSE. Dentin collagen treated by 1% MAGSE for 30 s was scarcely digested (1.6 ± 1.6%) after 1 h in 0.1% collagenase, while untreated collagen was completely digested (100.9 ± 20.2%). SEM/TEM images indicated MAGSE efficiently crosslinked dentin collagen in 30 s and rendered it almost inert to digestion under clinically relevant settings. Unlike GSE that hindered light-curing of HEMA, MAGSE accelerated the rate of polymerization and exhibited typical traits of a resin monomer with multiple polymerizable units. In conclusion, a novel collagen crosslinking resin MAGSE is synthesized, which inherits collagen crosslinking ability from GSE and polymerization function from MA. Inclusion of this light-curable collagen crosslinker into adhesives might be a revolutionary way to improve durability of dentin bonding in composite restorations.
目前,胶粘剂通过混合层中的微观互锁机制与牙本质结合。除了这种机械保持力外,与牙本质的结合还将受益于胶原和树脂之间的额外化学相互作用。本研究旨在合成一种新型的光固化胶原交联剂甲基丙烯酰基(MA)功能化葡萄籽提取物(GSE),并评估 MAGSE 在临床相关环境下交联牙本质胶原的能力以及作为树脂的光固化作用。通过用甲基丙烯酰氯反应 GSE 来完成 MA 功能化,以获得 MAGSE,并用 H-NMR 和傅里叶变换红外光谱(FTIR)对其进行表征。6-μm 厚的牙本质薄膜从第三磨牙的牙本质板上微切割。脱矿化后,用 1% MAGSE 处理 30 秒。通过 FTIR、薄膜的基质辅助激光解吸电离飞行时间质谱(MALDI-TOF)分析和板上的扫描电子显微镜(SEM)/透射电子显微镜(TEM)评估 MAGSE 的胶原交联和抗消化能力。同时,将 1% MAGSE 或 GSE 添加到含有 2-羟乙基甲基丙烯酸酯和三组分光引发剂系统的实验性胶粘剂中。使用 FTIR-衰减全反射连续 10 分钟实时监测聚合动力学。结果表明,MAGSE 可以与牙本质胶原结合,并像 GSE 一样保护其免受胶原酶降解。在 0.1%胶原酶中孵育 1 小时后,用 1% MAGSE 处理 30 秒的牙本质胶原仅被消化 1.6±1.6%,而未经处理的胶原则被完全消化(100.9±20.2%)。SEM/TEM 图像表明 MAGSE 在 30 秒内有效交联牙本质胶原,并使其在临床相关条件下几乎不被消化。与 GSE 阻碍 HEMA 的光固化不同,MAGSE 加速了聚合速率,并表现出具有多个聚合单元的树脂单体的典型特征。总之,合成了一种新型的胶原交联树脂 MAGSE,它继承了 GSE 的胶原交联能力和 MA 的聚合功能。将这种可光固化的胶原交联剂纳入胶粘剂中可能是一种革命性的方法,可以提高复合修复体中牙本质粘结的耐久性。