Dental Materials Laboratory, School of Dentistry, Federal University of Rio Grande do Sul, Porto Alegre, RS, Brazil.
Clinic for Masticatory Disorders and Dental Biomaterials, Center for Dental Medicine, University of Zurich, Zurich, Switzerland.
Dent Mater. 2024 Oct;40(10):1685-1691. doi: 10.1016/j.dental.2024.07.023. Epub 2024 Aug 2.
To formulate an experimental methacrylate-based photo-polymerizable resin for 3D printing with ytterbium trifluoride as filler and to evaluate the mechanical, physicochemical, and biological properties.
Resin matrix was formulated with 60 wt% UDMA, 40 wt% TEGDMA, 1 wt% TPO, and 0.01 wt% BHT. Ytterbium Trifluoride was added in concentrations of 1 (G), 2 (G), 3 (G), 4 (G), and 5 (G) wt%. One group remained without filler addition as control (G). The samples were designed in 3D builder software and printed using a UV-DLP 3D printer. The samples were ultrasonicated with isopropanol and UV cured for 60 min. The resins were tested for degree of conversion (DC), flexural strength, Knoop microhardness, softening in solvent, radiopacity, colorimetric analysis, and cytotoxicity (MTT and SRB).
Post-polymerization increased the degree of conversion of all groups (p < 0.05). G showed the highest DC after post-polymerization. G showed no differences in flexural strength from the G and G (p > 0.05). All groups showed a hardness reduction after solvent immersion. No statistical difference was found in radiopacity, softening in solvent (ΔKHN%), colorimetric spectrophotometry, and cytotoxicity (MTT) (p > 0.05). G showed reduced cell viability for SRB assay (p < 0.05).
It was possible to produce an experimental photo-polymerizable 3D printable resin with the addition of 2 % ytterbium trifluoride as filler without compromising the mechanical, physicochemical, and biological properties, comparable to the current provisional materials.
用氟化镱作为填料,配制一种实验性的甲基丙烯酸酯基光聚合树脂,用于 3D 打印,并评估其机械、物理化学和生物学性能。
树脂基质由 60wt% UDMA、40wt% TEGDMA、1wt% TPO 和 0.01wt% BHT 组成。氟化镱以 1(G)、2(G)、3(G)、4(G)和 5(G)wt%的浓度加入。一组保持不添加填料作为对照(G)。使用 3D 构建软件设计样品,使用 UV-DLP 3D 打印机打印。将样品用异丙醇超声处理,然后用 UV 光固化 60 分钟。测试树脂的转化率(DC)、弯曲强度、努普硬度、溶剂软化、射线不透性、比色分析和细胞毒性(MTT 和 SRB)。
后聚合使所有组的转化率都增加(p<0.05)。G 组在聚合后显示出最高的 DC。G 组的弯曲强度与 G 和 G 组无差异(p>0.05)。所有组在溶剂浸泡后硬度都降低。射线不透性、溶剂软化(ΔKHN%)、比色分光光度法和细胞毒性(MTT)均无统计学差异(p>0.05)。G 组的 SRB 检测显示细胞活力降低(p<0.05)。
在不影响机械、物理化学和生物学性能的情况下,加入 2wt%氟化镱作为填料,成功制备了一种实验性的光聚合 3D 打印树脂,与目前的临时材料相当。