Bor Sabahattin, Kaya Yeşim, Demiral Ayşe, Güngörmüş Mustafa
Department of Orthodontics, Faculty of Dentistry, İnönü University, Malatya 44280, Türkiye.
Department of Orthodontics, Faculty of Dentistry, Ankara Yıldırım Beyazıt University, Ankara 06760, Türkiye.
Polymers (Basel). 2025 Jun 26;17(13):1776. doi: 10.3390/polym17131776.
This study aimed to evaluate the cytotoxicity of two resin materials, Tera Harz TC-85 DAC and Clear-A, along with the effects of two different post-printing protocols applied to Clear-A. Samples were produced using the Ackuretta Sol printer. The following three groups were formed based on the resins used and the post-curing methods applied: Group 1: Tera Harz TC-85 DAC resin + Tera Harz Cure; Group 2: Clear-A resin + Curie machine; and Group 3: Clear-A resin + Tera Harz Cure. All samples were sterilized in 70% ethanol for 5 min, rinsed with sterile deionized water, and incubated in Dulbecco's Modified Eagle Medium at 37 °C for 72 h. Cytotoxicity assessment was performed by the XTT and RTCA methods using the human gingival fibroblast cell line. According to the XTT assay, undiluted resin extracts exhibited approximately 75-80% cell viability at 24 h, while further dilutions resulted in a viability exceeding 90%. No significant differences in viability were observed among the groups at any dilution at 48 and 72 h. The xCELLigence RTCA results aligned with the XTT findings, showing a transient decrease in cell viability within the first 24 h, followed by continued cell growth. This study demonstrated that extracts from all tested 3D-printed resins exhibited biocompatibility with human gingival fibroblasts. These findings support their potential for further applications in the dental and biomedical fields.
本研究旨在评估两种树脂材料(Tera Harz TC - 85 DAC和Clear - A)的细胞毒性,以及应用于Clear - A的两种不同后处理方案的效果。使用Ackuretta Sol打印机制作样本。根据所使用的树脂和应用的后固化方法形成以下三组:第1组:Tera Harz TC - 85 DAC树脂 + Tera Harz Cure;第2组:Clear - A树脂 + 居里机;第3组:Clear - A树脂 + Tera Harz Cure。所有样本在70%乙醇中灭菌5分钟,用无菌去离子水冲洗,并在37°C的杜氏改良 Eagle培养基中孵育72小时。使用人牙龈成纤维细胞系通过XTT和RTCA方法进行细胞毒性评估。根据XTT分析,未稀释的树脂提取物在24小时时表现出约75 - 80%的细胞活力,而进一步稀释导致活力超过90%。在48小时和72小时时,任何稀释度下各组之间的活力均未观察到显著差异。xCELLigence RTCA结果与XTT结果一致,显示在最初24小时内细胞活力短暂下降,随后细胞持续生长。本研究表明,所有测试的3D打印树脂提取物均表现出与人牙龈成纤维细胞的生物相容性。这些发现支持了它们在牙科和生物医学领域进一步应用的潜力。