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Polymerization- and Solvent-Induced Phase Separation in Hydrophilic-rich Dentin Adhesive Mimic

机译:富亲水性牙本质胶模拟物中的聚合和溶剂诱导的相分离

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摘要

Current dental resin undergoes phase separation into hydrophobic-rich and hydrophilic-rich phases during infiltration of the over-wet demineralized collagen matrix. Such phase separation undermines the integrity and durability of the bond at the composite/tooth interface. This study marks the first time that the polymerization kinetics of model hydrophilic-rich phase of dental adhesive has been determined. Samples were prepared by adding varying water content to neat resins made from 95 and 99wt% hydroxyethylmethacrylate (HEMA) and 5 and 1wt% (2,2-bis[4-(2-hydroxy-3-methacryloxypropoxy)phenyl1]-propane (BisGMA) prior to light curing. Viscosity of the formulations decreased with increased water content. The photo-polymerization kinetics study was carried out by time-resolved FTIR spectrum collector. All of the samples exhibited two-stage polymerization behavior which has not been reported previously for dental resin formulation. The lowest secondary rate maxima were observed for water content of 10-30%wt. Differential scanning calorimetry (DSC) showed two glass transition temperatures for the hydrophilic-rich phase of dental adhesive. The DSC results indicate that the heterogeneity within the final polymer structure decreased with increased water content. The results suggest a reaction mechanism involving both polymerization-induced phase separation (PIPs) and solvent-induced phase separation (SIPs) for the model hydrophilic-rich phase of dental resin.
机译:当前的牙科树脂在过湿的脱矿质胶原蛋白基质渗透期间经历相分离成富疏水相和富亲水相。这种相分离破坏了复合材料/牙齿界面处的粘结的完整性和耐久性。这项研究标志着首次确定了牙科胶粘剂模型富亲水相的聚合动力学。通过向95和99wt%的甲基丙烯酸羟乙酯(HEMA)和5和1wt%的(2,2-双[4-(2-羟基-3-甲基丙烯酰氧基丙氧基)苯基1]-丙烷(BisGMA)制成的纯树脂中添加不同的水含量来制备样品在光固化之前),配方的粘度随含水量的增加而降低,光聚合动力学研究是通过时间分辨FTIR光谱收集器进行的,所有样品均表现出两阶段的聚合行为,以前没有报道过。牙科树脂配方,水含量为10-30%wt时,次生速率最大值最低;差示扫描量热法(DSC)显示牙科胶粘剂的富亲水相有两个玻璃化转变温度,DSC结果表明,最终的聚合物结构随着水含量的增加而降低。结果表明反应机理涉及聚合诱导的相分离(PIP)和溶剂诱导的相分离牙科树脂的模型亲水性丰富阶段的化学修饰(SIP)。

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