Annisa Mutiara, Irnawati Dyah, Siswomihardjo Widowati, Sunarintyas Siti
Department of Dental Biomaterials, Faculty of Dentistry, Universitas Gadjah Mada, Yogyakarta,Indonesia.
J Dent Res Dent Clin Dent Prospects. 2024 Spring;18(2):129-134. doi: 10.34172/joddd.40900. Epub 2024 Jun 24.
Synthetic fibers have many benefits in clinical practice; however, they cause microplastic pollution, and their unaffordable price increases treatment costs. Natural silk fibers require biocompatibility assessment. This study investigated the effects of natural and synthetic fiber-reinforced composites (FRCs) on the cytotoxicity of fibroblast cell lines.
Three commercial synthetic fibers (polyethylene, quartz, and E-glass) and two silk fibers from and cocoons were employed. These fibers were made into FRC samples (n=6) by impregnation in flowable composite using a brass mold (25×2×2 mm). NIH/3T3 mouse fibroblasts were cultured in Dulbecco's modified eagle medium, supplemented, and seeded in 2×10 cells/mL. They were stored at 37 °C under 5% CO for 24 hours. The FRC samples were made into powder, eluted in dimethylsulfoxide, continued with PBS, supplemented with Dulbecco's modified eagle medium (DMEM), and exposed to cells for 24 hours. Blank (medium only) and control (cells and medium) samples were included. Subsequently, MTT was added for 4 h and read by enzyme-linked immunosorbent assay (λ=570 nm). Cell viability (%) was calculated and analyzed using one-way ANOVA (α=0.05).
All groups of FRCs showed>80% cell viability. One-way ANOVA showed no significant difference between FRC groups regarding the viability of fibroblast cell lines (>0.05).
Both natural silk and synthetic fibers exhibit low cytotoxicity to fibroblast cell lines. and silk fibers showed the potential to be used as alternative synthetic fibers.
合成纤维在临床实践中有诸多益处;然而,它们会造成微塑料污染,且价格高昂会增加治疗成本。天然丝纤维需要进行生物相容性评估。本研究调查了天然和合成纤维增强复合材料(FRCs)对成纤维细胞系细胞毒性的影响。
使用了三种商业合成纤维(聚乙烯、石英和E玻璃)以及来自 和 茧的两种丝纤维。通过使用黄铜模具(25×2×2毫米)将这些纤维浸渍在可流动复合材料中制成FRC样品(n = 6)。NIH/3T3小鼠成纤维细胞在杜氏改良 Eagle培养基中培养,添加相应成分,并以2×10个细胞/毫升的密度接种。将它们在37°C、5%二氧化碳条件下储存24小时。将FRC样品制成粉末,用二甲基亚砜洗脱,接着用PBS冲洗,再添加杜氏改良 Eagle培养基(DMEM),并与细胞接触24小时。包括空白(仅培养基)和对照(细胞和培养基)样品。随后,加入MTT 4小时,通过酶联免疫吸附测定法(λ = 570纳米)读取结果。计算细胞活力(%)并使用单因素方差分析(α = 0.05)进行分析。
所有FRCs组的细胞活力均>80%。单因素方差分析显示,FRC组之间在成纤维细胞系活力方面无显著差异(>0.05)。
天然丝纤维和合成纤维对成纤维细胞系均表现出低细胞毒性。 和 丝纤维显示出作为替代合成纤维使用的潜力。