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Polymerization shrinkage kinetics and degree of conversion of commercial and experimental resin modified glass ionomer luting cements (RMGICs)

机译:聚合收缩动力学和商业和实验树脂改性玻璃离聚物排放水泥的转化程度(RMGICS)

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Objectives. Tetrahydrofurfuryl-methacrylate (THFM) and hydroxypropyl-methacrylate (HPM) were used to partially or fully replace HEMA in experimental RMGICs. The experimental materials were compared with home and commercial products in terms of degree of conversion, polymerization shrinkage and exotherm.Methods. Two commercial RMGICs used were Fuji-Plus (FP, GC, Japan) and RelyX-Luting (RX, 3M-ESPE, USA). Two additional in-house liquids were prepared based on the commercial materials liquids. Eight experimental liquid compositions (F1, F2, F3 and F4 based on Fuji-Plus; R1, R2, R3 and R4 based on RelyX-Luting) were prepared replacing 100% HEMA with HPM in F1 and R1 or 70%/30% HPM/THFM in F2 and R2. 50% HEMA was replaced with THFM in F3 and R3 compared to 30% in F4 and R4. All liquids were mixed with the corresponding commercial powder. Degree of conversion was determined using Fourier-transform infrared spectroscopy (FT-IR). Polymerization shrinkage and exotherm were measured using the bonded-disk method.Results. Compositions containing HPM (F1 and R1) showed lower degree of conversion compared to experimental compositions containing THFM, home and commercial materials (p 0.0001). FP-commercial showed significantly higher polymerization shrinkage and exotherm compared to all other materials in both groups (p 0.0001). FP-commercial showed higher degree of polymerization shrinkage and exotherm at 5 min compared to all materials due to the incorporation of an additional cross-linker (glycerol-dimethacrylate). In general, compositions containing THFM, presented polymerization shrinkage and degree of conversion values similar to their corresponding commercial products.Significance. THFM monomer showed promising results and could be potentially useful in the development of new RMGICs with improved properties. (C) 2020 The Academy of Dental Materials. Published by Elsevier Inc. All rights reserved.
机译:目标。使用四氢呋喃基 - 甲基丙烯酸甲酯(THFM)和羟丙基 - 甲基丙烯酸酯(HPM)在实验性RMGICS中部分或完全替代HEMA。在转化程度,聚合收缩和放热方面将实验材料与家庭和商业产品进行比较。使用的两家商业资源富士加(FP,GC,日本)和楼梯索(RX,3M-ESPE,USA)。基于商业材料液体制备两种额外的内部液体。基于FUJI-PLUS的八种实验液组合物(F1,F2,F3和F4; R1,R2,R3和R4,在F1和R1或70%/ 30%HPM中用HPM替换100%HEMA / THFM在F2和R2中。在F3和R3中替换50%HEMA,与F4和R4相比,R3相比。将所有液体与相应的商业粉末混合。使用傅立叶变换红外光谱(FT-IR)测定转化程度。使用键合磁盘法测量聚合收缩和放热。结果。与含有THFM,家庭和商业材料的实验组合物相比,含有HPM(F1和R1)的组合物显示出较低的转化率(P <0.0001)。与两组中的所有其他材料相比,FP-Commertic展示了显着更高的聚合收缩和放热(P <0.0001)。由于掺入额外的交联剂(甘油 - 二甲基丙烯酸酯),FP-Commertic在5分钟内显示出更高的聚合收缩和放热。通常,含有THFM的组合物,呈现聚合收缩和与其相应的商业产品类似的转化值。重要性。 THFM单体表明有希望的结果,可能在开发新的RMGICS具有改进的性质方面可能有用。 (c)2020牙科材料学院。由elsevier Inc.出版的所有权利保留。

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