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A Novel Multi-Cross-linking Diluent System to Stabilize Self-Etch Bonding

胶粘剂 甲基丙烯酸酯 接触角 材料科学 润湿 稀释剂 傅里叶变换红外光谱 化学工程 衰减全反射 甲基丙烯酸羟乙基酯 牙本质 甲基丙烯酸缩水甘油酯 复合材料 丙烯酸树脂 牙髓(牙) 明胶 红外光谱学 疏水 粘结强度 壳聚糖 粘接 耐久性 化学 高分子化学 牙科粘接 复合数
作者
Zilu Tian,Yu Zhu,Shihui Yang,H.M. Wang,Q. H. Bai,X. Z. Han,Shuwei Qiao,Zuosen Shi,Song Zhu
出处
期刊:Journal of Dental Research [SAGE Publishing]
卷期号:: 220345261457339-220345261457339
标识
DOI:10.1177/00220345261457339
摘要

Despite the indispensability of 2-hydroxyethyl methacrylate (HEMA) for improving the wettability of self-etch (SE) adhesives, elevated concentration may compromise the durability of the hybrid layer. This study proposes a modification strategy to preserve the wettability of SE adhesives while reducing excessive HEMA content and enhancing hybrid layer integrity through introducing collagen-protective and hydrophobic features. Thus, a novel diluent system was developed by partially replacing HEMA with 2 hydrophobic cross-linking reagents, 3-(4-formylphenoxy)-2-hydroxypropyl methacrylate (FPA) and glycidyl methacrylate (GMA). Attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR), confocal laser scanning microscopy (CLSM), wettability, and water contact angle analyses confirmed that FPA induced rapid but transient cross-linking with collagen. Thus, the compatibility of collagen with hydrophobic adhesives was improved. The time-dependent cross-linking efficacy of GMA was evaluated by ATR-FTIR and sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Guided by these findings, FPA-GMA adhesives were formulated and subjected to physicochemical (flexural strength, Vickers microhardness, and water sorption/solubility) and biological (Cell Counting Kit-8, calcein acetoxymethyl ester/propidium iodide) evaluations. Enzymatic degradation assays, including in situ zymography, gelatin zymography, and the hydroxyproline releasing test, verified that FPA-GMA adhesives built the degradation-resistant hybrid layer during dentin bonding. CLSM, micro-tensile bond strength, and nanoleakage analysis corroborated the establishment of a stable and durable FPA-GMA dentin-bonding interface before and after 10,000 thermocycles. Collectively, this study evaluated whether FPA-GMA formulations improve the physicochemical properties of experimental adhesives and their biological/functional interactions with dentin, as assessed by enzymatic activity and bonding performance at the dentin-bonding interface. The results demonstrated that FPA-GMA provided sustained collagen protection while preserving SE infiltration and enhancing its mechanical properties, which thereby improved the durability of the dentin-bonding interface.
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