含星爆单体的高性能牙科树脂。

Journal of dental research Pub Date : 2024-05-01 Epub Date: 2024-03-28 DOI:10.1177/00220345241232312
S Q Dai, W Zhou, L Y Duan, K Tang, Z Y Yang, R J Cao, F R Tay, L N Niu, J H Chen
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引用次数: 0

摘要

基于二甲基丙烯酸酯的化学物质因其卓越的综合性能而被广泛用作牙科树脂基材料的树脂单体。然而,它也面临着机械性能不足、体积收缩和雌激素性等挑战。在此,我们首先通过接枝-本体法合成了一种新型树脂单体--9-臂星形聚氨酯丙烯酸酯(NPUA)。与主要的商用牙科单体 2,2-双[对-(2'-羟基-3'-甲基丙烯酰氧基丙氧基)苯基]丙烷(Bis-GMA)(粘度为 1,174 ± 3 Pa-s,体积收缩率为 4.7% ± 0.1%)相比,NPUA 单体的粘度(158 ± 1 Pa-s)、体积收缩率(2.5% ± 0.1%)和细胞毒性(P < 0.05)都更低。与 Bis-GMA(70 wt%)/TEGDMA(30 wt%)树脂相比,NPUA 基树脂具有更高的抗弯强度、抗弯模量、硬度和疏水性,以及更低的体积收缩率、吸水性和溶解性。与 Bis-GMA 组(分别为 120.3 ± 4.7 MPa、9.4 ± 0.7 GPa、1.5 ± 0.1 GPa 和 4.7% ± 0.2%;P < 0.05)相比,NPUA 基复合材料的抗弯强度、抗弯模量和硬度明显更高,体积收缩率更低(分别为 171.4 ± 3.0 MPa、12.6 ± 0.5 GPa、2.0 ± 0.2 GPa 和 3.4% ± 0.2%)。这项研究为提高牙科树脂的物理化学属性提供了一条可行的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-Performance Dental Resins Containing a Starburst Monomer.

Dimethacrylate-based chemistries feature extensively as resin monomers in dental resin-based materials due to their distinguished overall performance. However, challenges endure, encompassing inadequate mechanical attributes, volumetric shrinkage, and estrogenicity. Herein, we first synthesized a novel resin monomer, 9-armed starburst polyurethane acrylate (NPUA), via the grafting-onto approach. Compared to the primary commercial dental monomer 2,2-bis [p-(2'-hydroxy-3'-methacryloxypropoxy) phenyl] propane (Bis-GMA) (with a viscosity of 1,174 ± 3 Pa·s and volumetric shrinkage of 4.7% ± 0.1%), the NPUA monomer achieves the lower viscosity (158 ± 1 Pa·s), volumetric shrinkage (2.5% ± 0.1%), and cytotoxicity (P < 0.05). The NPUA-based resins exhibit the higher flexural strength, flexural modulus, hardness, and hydrophobicity and lower volumetric shrinkage, water absorption, and solubility compared to the Bis-GMA (70 wt%)/TEGDMA (30 wt%) resins. The NPUA-based composites exhibit significantly higher flexural strength, flexural modulus, and hardness and lower volumetric shrinkage (171.4 ± 3.0 MPa, 12.6 ± 0.5 GPa, 2.0 ± 0.2 GPa, and 3.4% ± 0.2%, respectively) compared to the Bis-GMA group (120.3 ± 4.7 MPa, 9.4 ± 0.7 GPa, 1.5 ± 0.1 GPa, and 4.7% ± 0.2%, respectively; P < 0.05). This work presents a viable avenue for augmenting the physicochemical attributes of dental resins.

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