Theaflavin −3,3'-digallate/ethanol: a novel cross-linker for stabilizing dentin collagen

Zhiyong Chen, Yingxian Wei, Likun Liang, Xu Wang, Fangfei Peng, Yiying Liang, Xin Huang, Kaiqi Yan, Yunxia Gao, Kangjing Li, Xiaoman Huang, Xinglu Jiang, Wenxia Chen
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Abstract

To study the ability of theaflavin-3,3’-digallate (TF3)/ethanol solution to crosslink demineralized dentin collagen, resist collagenase digestion, and explore the potential mechanism.Fully demineralized dentin blocks were prepared using human third molars that were caries-free. Then, these blocks were randomly allocated into 14 separate groups (n = 6), namely, control, ethanol, 5% glutaraldehyde (GA), 12.5, 25, 50, and 100 mg/ml TF3/ethanol solution groups. Each group was further divided into two subgroups based on crosslinking time: 30 and 60 s. The efficacy and mechanism of TF3’s interaction with dentin type I collagen were predicted through molecular docking. The cross-linking, anti-enzymatic degradation, and biomechanical properties were studied by weight loss, hydroxyproline release, scanning/transmission electron microscopy (SEM/TEM), in situ zymography, surface hardness, thermogravimetric analysis, and swelling ratio. Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy were utilized to explore its mechanisms. Statistical analysis was performed using one and two-way analysis of variance and Tukey’s test.TF3/ethanol solution could effectively crosslink demineralized dentin collagen and improve its resistance to collagenase digestion and biomechanical properties (p < 0.05), showing concentration and time dependence. The effect of 25 and 50 mg/ml TF3/ethanol solution was similar to that of 5% GA, whereas the 100 mg/mL TF3/ethanol solution exhibited better performance (p < 0.05). TF3 and dentin type I collagen are mainly cross-linked by hydrogen bonds, and there may be covalent and hydrophobic interactions.TF3 has the capability to efficiently cross-link demineralized dentin collagen, enhancing its resistance to collagenase enzymatic hydrolysis and biomechanical properties within clinically acceptable timeframes (30 s/60 s). Additionally, it exhibits promise in enhancing the longevity of dentin adhesion.
茶黄素-3,3'-二镓酸酯/乙醇:稳定牙本质胶原蛋白的新型交联剂
研究黄素-3,3'-二镓酸酯(TF3)/乙醇溶液交联脱矿牙本质胶原蛋白、抵抗胶原酶消化的能力,并探索其潜在机制。然后,将这些牙本质块随机分配到 14 个不同的组别(n = 6),即对照组、乙醇组、5% 戊二醛(GA)组、12.5、25、50 和 100 mg/ml TF3/乙醇溶液组。每组又根据交联时间分为两个亚组,分别为 30 秒和 60 秒:通过分子对接预测了 TF3 与牙本质 I 型胶原相互作用的功效和机制。通过失重、羟脯氨酸释放、扫描/透射电子显微镜(SEM/TEM)、原位酶标仪、表面硬度、热重分析和膨胀率等方法研究了交联、抗酶降解和生物力学特性。傅立叶变换红外光谱(FTIR)、X 射线光电子能谱(XPS)和拉曼光谱被用来探索其机理。TF3/乙醇溶液能有效交联脱矿化牙本质胶原,提高其抗胶原酶消化能力和生物力学性能(p < 0.05),并表现出浓度和时间依赖性。25和50毫克/毫升TF3/乙醇溶液的效果与5% GA相似,而100毫克/毫升TF3/乙醇溶液的效果更好(p < 0.05)。TF3 与牙本质 I 型胶原主要通过氢键交联,也可能存在共价和疏水相互作用。TF3 能够在临床可接受的时间范围内(30 秒/60 秒)有效交联脱矿牙本质胶原,增强其抗胶原酶酶水解的能力和生物力学特性。此外,它还有望提高牙本质粘附的寿命。
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