Effect of post-printing curing time on cytotoxicity of direct printed aligners: A pilot study.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Giorgio Iodice, Bjorn Ludwig, Elena Polishchuk, Raffaella Petruzzelli, Roberto Di Cunto, Soboh Husam, Mauro Farella
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引用次数: 0

Abstract

Introduction: The aim of this in vitro study was to examine the potential impact of different curing times of 3D-printed orthodontic aligners on their cytotoxicity.

Method: Some 60 samples of aligner material were directly 3D printed using Tera Harz TC-85 DAC resin and randomly allocated to three different curing time groups (14, 24 and 50 min). Zendura FLX samples were used as control. The samples were incubated in saliva for 14 days, and then the supernatant was collected. Human gingival fibroblasts (HGF-1)-CRL2014 were used to evaluate potential cytotoxicity. Furthermore, HGF-1 cells were plated on the samples as well as on a glass control sample. After 72 h of growth, their viability was tested.

Results: Compared with the glass, only the 50-min curing time markedly reduced fibroblast cell growth. Additionally, a negative linear trend was observed between curing time and fibroblast growth. In comparison with the aligner control group, all samples, including the aligner control samples, exhibited a significant reduction in the viability of human fibroblasts when exposed to saliva.

Conclusions: 3D directly printed aligners showed a cytotoxic effect similar to that of thermoformed conventional aligners in terms of fibroblasts growth. A linear trend was found between curing time and cells growth, indicating that directly printed aligners could exhibit higher cytotoxicity if exposed to a longer curing time. This dependence on curing time underscores the importance of following a strict manufacturing process.

印刷后固化时间对直接印刷校准器细胞毒性的影响:试点研究
简介:这项体外研究的目的是检测 3D 打印正畸矫治器不同的固化时间对其细胞毒性的潜在影响:这项体外研究的目的是检测 3D 打印正畸矫治器不同固化时间对其细胞毒性的潜在影响:方法:使用 Tera Harz TC-85 DAC 树脂直接 3D 打印约 60 个矫正器材料样品,并随机分配到三个不同固化时间组(14、24 和 50 分钟)。Zendura FLX 样品用作对照组。样品在唾液中培养 14 天,然后收集上清液。人牙龈成纤维细胞(HGF-1)-CRL2014 用于评估潜在的细胞毒性。此外,还将 HGF-1 细胞培养在样品和玻璃对照样品上。生长 72 小时后,检测其存活率:结果:与玻璃相比,只有固化时间为 50 分钟的样品能明显减少成纤维细胞的生长。此外,固化时间与成纤维细胞生长之间呈负线性趋势。与对准器对照组相比,包括对准器对照组在内的所有样品在暴露于唾液中时,人成纤维细胞的活力都显著降低:结论:在成纤维细胞生长方面,三维直接打印对齐器显示出与热成型传统对齐器相似的细胞毒性效应。固化时间与细胞生长之间呈线性趋势,这表明如果固化时间较长,直接打印的对准器会表现出更高的细胞毒性。这种对固化时间的依赖性强调了严格遵守生产流程的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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