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双酚A缩水甘油甲基丙烯酸酯替代低聚物脂环族聚酯二甲基丙烯酸酯的可见光固化特性

Visible light cure characteristics of a cycloaliphatic polyester dimethacrylate alternative oligomer to bisGMA.

作者信息

Vaidyanathan Tritala K, Vaidyanathan Jayalakshmi

机构信息

Department of Restorative Dentistry, Rutgers School of Dental MedicineNewarkNJUSA.

出版信息

Acta Biomater Odontol Scand. 2015 Sep 18;1(2-4):59-65. doi: 10.3109/23337931.2015.1085806. eCollection 2015 Dec.

Abstract

: The goal of this study was to characterize the light curing characteristics of a new oligomer PEM-665 designed to be used as an alternative monomer to BisGMA. : PEM-665 (P) and BisGMA (B) solutions were prepared with triethylene glycol dimethacrylate (T) diluent in different weight proportions (70/30 and 50/50). Solutions containing 70% P and 30% T were designated as 70PT, 70%B and 30%T as 70BT, 50%P and 50%T as 50PT and 50%B and 50%T as 50BT. The initiators were CQ (EDMAB was used as amine accelerator for CQ) and DPO in 1% concentration. Eight solutions were prepared in a factorial design: 70PT/DPO; 70PT/CQ; 50PT/DPO; 50PT/CQ; 70BT/DPO; 70BT/CQ; 50BT/DPO; 50BT/CQ. BISCO VIP visible light was used to cure the monomer solutions using 30 s exposure time and 400 W power setting. TA Instruments Differential Scanning Calorimeter (DSC 2910) was used to determine the heat of cure (J/g) during polymerization at 37 °C, from which molar heat of cure (kJ/mole) and %Conversion values were estimated. : Range of mean values as a function monomer selections were: heat of cure (J/g): 161.7 for 70PT/DPO system to 198.6 for 50BT/CQ system; molar heat of cure (kJ/mole): 67.3 for 70BT/DPO to 78.86 for 50PT/CQ; % conversion: 59.9 for 70BT/DPO to 70.3 for 50PT/CQ. Analysis of variance and Tukey HSD pairwise contrast showed statistically significant differences between % conversion means of PEM and BisGMA mixtures, with PEM mixtures showing significantly higher mean values. : The results suggest that PEM-665 is a promising candidate material for dental polymer applications.

摘要

本研究的目的是表征一种新型低聚物PEM - 665的光固化特性,该低聚物被设计用作BisGMA的替代单体。用二缩三乙二醇二甲基丙烯酸酯(T)稀释剂按不同重量比例(70/30和50/50)制备PEM - 665(P)和BisGMA(B)溶液。含70% P和30% T的溶液指定为70PT,70% B和30% T为70BT,50% P和50% T为50PT,50% B和50% T为50BT。引发剂为浓度1%的CQ(EDMAB用作CQ的胺促进剂)和DPO。采用析因设计制备了八种溶液:70PT/DPO;70PT/CQ;50PT/DPO;50PT/CQ;70BT/DPO;70BT/CQ;50BT/DPO;50BT/CQ。使用BISCO VIP可见光以30秒曝光时间和400瓦功率设置固化单体溶液。使用TA仪器差示扫描量热仪(DSC 2910)测定37℃聚合过程中的固化热(J/g),据此估算摩尔固化热(kJ/摩尔)和转化率百分比值。作为单体选择函数的平均值范围为:固化热(J/g):70PT/DPO体系为161.7至50BT/CQ体系为198.6;摩尔固化热(kJ/摩尔):70BT/DPO为67.3至50PT/CQ为78.86;转化率百分比:70BT/DPO为59.9至50PT/CQ为70.3。方差分析和Tukey HSD成对对比显示,PEM和BisGMA混合物的转化率平均值之间存在统计学显著差异,PEM混合物的平均值显著更高。结果表明,PEM - 665是牙科聚合物应用中有前景的候选材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d584/5433180/d6e423bf01fc/iabo_a_1085806_f0002_c.jpg

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