Volpe Research Center, American Dental Association Foundation, Gaithersburg, MD, USA.
Division of Molecular and Regenerative Prosthodontics, Graduate School of Dentistry, Tohoku University, Sendai, Japan.
J Dent Res. 2020 Feb;99(2):189-195. doi: 10.1177/0022034519895269. Epub 2019 Dec 20.
Dental adhesives are vital for the success of dental restorations. The objective of this study is to make strong and durable dental adhesives that are free from 2 symbolic methacrylate-based dental resins-2-bis[4-(2-hydroxy-3-methacryl-oxypropoxy)-phenyl]-propane (Bis-GMA) and 2-hydroxyethyl-methacrylate (HEMA)-and have equivalent/improved bonding strength and durability. We formulated, prepared, and evaluated 2 dental adhesives using mixtures of a hydrolytically stable ether-based monomer, triethylene glycol divinylbenzyl ether (TEG-DVBE), with urethane dimethacrylate (UDMA) or pyromellitic glycerol dimethacrylate. These adhesives were composed of equimolar ester-/ether-based vinyl functional groups. They were compared with Bis-GMA/HEMA-based commercial and experimental dental adhesives in terms of shear bond strength and microtensile bond strength (µTBS) to human dentin and the µTBS bond stability under extended thermocycling challenges. In addition, the resins' infiltration to dentin tubules, mechanical performance, and chemical properties were assessed by scanning electron microscopy, ISO standard flexural strength and modulus measurements, contact angle measurements, and water sorption/solubility measurements. The hybrid TEG-DVBE-containing dental adhesives generated equivalent shear bond strength and µTBS in comparison with the controls. Significantly, these adhesives outperformed the controls after being challenged by 10,000 thermocycles between 5 °C and 55 °C. Water contact angle measurements suggested that the hybrid dental adhesives were relatively more hydrophobic than the Bis-GMA/HEMA controls. However, both TEG-DVBE-containing adhesives developed more and deeper resin tags in dentin tubules and formed thicker hybrid layers at the composite-dentin interface. Furthermore, the water solubility of UDMA/TEG-DVBE resins was reduced approximately 89% in comparison with the Bis-GMA/HEMA controls. The relatively hydrophobic adhesives that achieved equivalent/enhanced bonding performance suggest great potentials in developing dental restoration with extended service life. Furthermore, the TEG-DVBE-containing materials may find wider dental applications and broader utility in medical device development.
牙科胶粘剂对于牙科修复的成功至关重要。本研究的目的是开发出不含两种具有象征意义的甲基丙烯酸酯基牙科树脂(双酚 A 二缩水甘油醚和 2-羟乙基甲基丙烯酸酯)的高强度和耐用的牙科胶粘剂,并具有同等/改善的粘结强度和耐久性。我们使用水解稳定的醚基单体三乙二醇二乙烯基苯醚(TEG-DVBE)与聚氨酯二甲基丙烯酸酯(UDMA)或均苯四甲酸二缩水甘油酯混合,配制、制备和评估了两种牙科胶粘剂。这些胶粘剂由等摩尔酯/醚基乙烯基官能团组成。它们在剪切粘结强度和微拉伸粘结强度(µTBS)与人牙本质的粘结以及在延长热循环挑战下的µTBS 粘结稳定性方面与 Bis-GMA/HEMA 为基础的商业和实验性牙科胶粘剂进行了比较。此外,通过扫描电子显微镜、ISO 标准弯曲强度和模量测量、接触角测量和吸水率/溶解度测量评估了树脂对牙本质小管的渗透、机械性能和化学性能。含有混合 TEG-DVBE 的牙科胶粘剂的剪切粘结强度和µTBS 与对照组相当。值得注意的是,在 5°C 和 55°C 之间经过 10000 次热循环挑战后,这些胶粘剂的性能优于对照组。水接触角测量表明,混合牙科胶粘剂相对比 Bis-GMA/HEMA 对照组更疏水。然而,两种含 TEG-DVBE 的胶粘剂在牙本质小管中形成了更多和更深的树脂标记,并在复合-牙本质界面上形成了更厚的混合层。此外,与 Bis-GMA/HEMA 对照组相比,UDMA/TEG-DVBE 树脂的水溶性降低了约 89%。具有相当粘结性能的相对疏水胶粘剂在开发具有延长使用寿命的牙科修复体方面具有巨大的潜力。此外,含 TEG-DVBE 的材料可能在牙科应用和医疗器械开发方面有更广泛的用途。