Alrahlah Ali, Al-Odayni Abdel-Basit, Saeed Waseem Sharaf, Abduh Naaser A Y, Khan Rawaiz, Alshabib Abdulrahman, Almajhdi Faisal Fahad N, Alodeni Riad M, De Vera Merry Angelyn Tan
Restorative Dental Sciences Department, College of Dentistry, King Saud University, Riyadh 11545, Saudi Arabia.
Engineer Abdullah Bugshan Research Chair for Dental and Oral Rehabilitation, College of Dentistry, King Saud University, Riyadh 11545, Saudi Arabia.
Polymers (Basel). 2023 Feb 23;15(5):1124. doi: 10.3390/polym15051124.
The aim of this work was to assess the limiting rate of eugenol (Eg) and eugenyl-glycidyl methacrylate (EgGMA) at which the ideal degree of conversion (DC) of resin composites is achieved. For this, two series of experimental composites, containing, besides reinforcing silica and a photo-initiator system, either EgGMA or Eg molecules at 0-6.8 wt% per resin matrix, principally consisting of urethane dimethacrylate (50 wt% per composite), were prepared and denoted as UGx and UEx, where x refers to the EgGMA or Eg wt% in the composite, respectively. Disc-shaped specimens (5 × 1 mm) were fabricated, photocured for 60 s, and analyzed for their Fourier transform infrared spectra before and after curing. The results revealed concentration-dependent DC, increased from 56.70% (control; UG0 = UE0) to 63.87% and 65.06% for UG3.4 and UE0.4, respectively, then dramatically decreased with the concentration increase. The insufficiency in DC due to EgGMA and Eg incorporation, i.e., DC below the suggested clinical limit (>55%), was observed beyond UG3.4 and UE0.8. The mechanism behind such inhibition is still not fully determined; however, radicals generated by Eg may drive its free radical polymerization inhibitory activity, while the steric hindrance and reactivity of EgGMA express its traced effect at high percentages. Therefore, while Eg is a severe inhibitor for radical polymerization, EgGMA is safer and can be used to benefit resin-based composites when used at a low percentage per resin.
这项工作的目的是评估丁香酚(Eg)和甲基丙烯酸缩水甘油酯丁香酚酯(EgGMA)的极限添加量,在该添加量下树脂复合材料可实现理想的转化率(DC)。为此,制备了两个系列的实验性复合材料,除增强二氧化硅和光引发剂体系外,每个树脂基体中含有0-6.8 wt%的EgGMA或Eg分子,树脂基体主要由二甲基丙烯酸聚氨酯(占复合材料的50 wt%)组成,分别记为UGx和UEx,其中x分别指复合材料中EgGMA或Eg的wt%。制作了圆盘状试样(5×1 mm),光固化60 s,并在固化前后对其进行傅里叶变换红外光谱分析。结果显示转化率与浓度有关,从56.70%(对照;UG0 = UE0)分别增至UG3.4的63.87%和UE0.4的65.06%,然后随着浓度增加急剧下降。在超过UG3.4和UE0.8时,观察到由于加入EgGMA和Eg导致转化率不足,即转化率低于建议的临床限值(>55%)。这种抑制作用背后的机制仍未完全确定;然而,Eg产生的自由基可能会驱动其自由基聚合抑制活性,而EgGMA的空间位阻和反应性在高比例时表现出其追踪效应。因此,虽然Eg是自由基聚合的严重抑制剂,但EgGMA更安全,当以低比例添加到树脂中时可用于改善树脂基复合材料。