Ogliari Fabrício A, Ely Caroline, Zanchi Cesar H, Fortes Carmen B B, Samuel Susana M W, Demarco Flávio Fernando, Petzhold Cesar L, Piva Evandro
Department of Operative Dentistry, School of Dentistry, Federal University of Pelotas, Rua Gonçalves Chaves, 457, CEP 96015-560, Pelotas, RS, Brazil.
Dent Mater. 2008 Feb;24(2):165-71. doi: 10.1016/j.dental.2007.03.007. Epub 2007 May 24.
To investigate the role of chain extender size from Bis-EMA monomers on the polymerization profiles and properties of the crosslinked polymers. Additionally, the influence of Bis-GMA was also evaluated.
The polymer network from homopolymers Bis-EMA4, Bis-EMA10 and Bis-EMA30 was characterized, as well as copolymers formed among these monomers and Bis-GMA. The degree of conversion from neat and blended monomers as a function of photo-activation time was evaluated by FTIR. Rate of polymerization, network parameter and cross-link density from materials were demonstrated. Water sorption and solubility were determined according to ISO 4049 specification and the data obtained were analyzed by two-way ANOVA/Tukey's test (alpha=0.05). Flexural strength and Young's modulus from polymerized monomers/co-monomers were measured after 24h water storage at 37 degrees C and the results were analyzed by one-way ANOVA/Tukey's test (alpha=0.05).
Monomers with larger ethylene oxide units presented the highest values regarding the degree of conversion and cross-link density. The effect of the chain extender length was also observed in water sorption and solubility polymer characteristics, with Bis-EMA4 being the most hydrophobic polymer. Bis-EMA10 and Bis-EMA30 homopolymers were not able to be tested with the three point bending test due to their great flexibility. The addition of Bis-GMA produced stronger and more rigid Bis-EMA polymers (p<0.05).
Aromatic dimethacrylates with different chain extender lengths can be a useful alternative in controlling the properties of a dental material, adjusting those to specific applications.
研究双甲基丙烯酸乙二酯(Bis-EMA)单体中扩链剂大小对交联聚合物聚合特性及性能的影响。此外,还评估了双甲基丙烯酸缩水甘油酯(Bis-GMA)的影响。
对Bis-EMA4、Bis-EMA10和Bis-EMA30均聚物的聚合物网络以及这些单体与Bis-GMA形成的共聚物进行了表征。通过傅里叶变换红外光谱(FTIR)评估纯单体和混合单体的转化率随光活化时间的变化。展示了材料的聚合速率、网络参数和交联密度。根据ISO 4049规范测定吸水率和溶解度,并通过双向方差分析/图基检验(α=0.05)对所得数据进行分析。在37℃下储存24小时水后,测量聚合单体/共聚单体的弯曲强度和杨氏模量,并通过单向方差分析/图基检验(α=0.05)对结果进行分析。
环氧乙烷单元较大的单体在转化率和交联密度方面呈现出最高值。在吸水率和聚合物溶解度特性方面也观察到了扩链剂长度的影响,其中Bis-EMA4是疏水性最强的聚合物。Bis-EMA10和Bis-EMA30均聚物由于其极大的柔韧性而无法进行三点弯曲试验。添加Bis-GMA可使Bis-EMA聚合物更强且更刚性(p<0.05)。
具有不同扩链剂长度的芳族二甲基丙烯酸酯可作为控制牙科材料性能、使其适应特定应用的有用替代品。