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Effect of eluates from zirconia-modified glass ionomer cements on DNA double-stranded breaks in human gingival fibroblast cells

机译:氧化锆改性的玻璃离子水门汀的洗出液对人牙龈成纤维细胞DNA双链断裂的影响

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摘要

Objective. To formulate novel glass ionomer cements (GICs) containing zirconia (nanopartides (NPs) and micro-particles (MPs)) and investigate the genotoxic effect of their eluates on DNA double-strand breaks of human gingival fibroblasts (HGFs) in vitro using a gamma-H2AX fluorescent assay.Methods. GIC (control, C), 10%ZrO(2)NPsGIC (T1) and 10%ZrO(2)MPsGIC (T2) were prepared per the manufacturer's instructions (hand-mixed, P/L =3.4:1 w/w%). Dulbecco's modified Eagle's medium (DMEM) was used as the culture medium for HGFs and for eluate preparation. Eluates were collected from all specimens (n = 5/g, 5 x 2 mm) after 24 h and used for XTT to obtain the EC50 using Graph Pad Prism4. A gamma-H2AX immunofluorescence assay was performed to detect DSBs in HGFs. The mean foci per cells and percentage of free foci cells were statistically compared (one-way ANOVA with Tamhane's post hoc and Chi-square respectively) (p 0.05).Results. (1) EC50 ranged from 31 to 36%. 5% and 20% eluate concentrations were selected for the genotoxicity test. (2) Cells exposed to eluates from T1 had lower mean foci per cell than cells in T2 and C eluates (p 0.05). Only cells in T1 at 5% had lower mean foci cell than medium (p 0.05). (3) T1 and C at both concentration showed a higher, but not significant, percentage of free foci cells than negative control (medium). At 20% eluate concentration T2 had a lower percentage of free foci cells than C (p 0.05).Significance. Nano-zirconia GIC and micro-zirconia GIC were formulated. GIC and both zirconia modified GICs had no genotoxic effect on HGFs in vitro. Further studies related to physical properties should be performed to determine the future clinical applications for these novel nanomaterials. (C) 2019 The Academy of Dental Materials. Published by Elsevier Inc. All rights reserved.
机译:目的。配制含有氧化锆(纳米颗粒(NPs)和微粒(MPs))的新型玻璃离聚物水泥(GIC),并研究其洗脱液对人类牙龈成纤维细胞(HGF)DNA双链断裂的遗传毒性作用。 -H2AX荧光测定法。按照制造商的说明制备GIC(对照,C),10%ZrO(2)NPsGIC(T1)和10%ZrO(2)MPsGIC(T2)(手工混合,P / L = 3.4:1 w / w% )。 Dulbecco改良的Eagle培养基(DMEM)用作HGF和洗脱液的培养基。 24小时后从所有标本中收集洗脱液(n = 5 / g,5 x 2 mm),并使用Graph Pad Prism4进行XTT获得EC50。进行了γ-H2AX免疫荧光检测,以检测HGF中的DSB。统计比较每个细胞的平均病灶和游离病灶细胞的百分比(分别用Tamhane的post hoc和卡方检验进行单向ANOVA)(p <0.05)。 (1)EC50为31%至36%。选择5%和20%的洗脱液浓度进行基因毒性测试。 (2)暴露于T1淋洗液的细胞的平均病灶低于T2和C淋洗液的细胞(p <0.05)。 T1中只有5%的细胞具有比培养基低的平均病灶细胞(p <0.05)。 (3)两种浓度下的T1和C均比阴性对照(中)显示出更高但不显着的游离灶细胞百分比。在20%的洗脱液浓度下,T2的游离灶细胞百分比低于C(p <0.05)。制定了纳米氧化锆GIC和微氧化锆GIC。 GIC和两种氧化锆修饰的GIC在体外对HGF均无遗传毒性作用。应该进行与物理性质有关的进一步研究,以确定这些新型纳米材料的未来临床应用。 (C)2019牙科材料学院。由Elsevier Inc.出版。保留所有权利。

著录项

  • 来源
    《Dental materials》 |2019年第3期|444-449|共6页
  • 作者单位

    Chulalongkorn Univ, Fac Dent, CU Dent Innovat Ctr, Henri Dunant 34, Bangkok 10330, Thailand;

    Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Conservat Dent & Periodontol, Munich, Germany|Ludwig Maximilians Univ Munchen, Walther Straub Inst Pharmacol & Toxicol, Fac Med, Munich, Germany;

    Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Conservat Dent & Periodontol, Munich, Germany;

    Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Conservat Dent & Periodontol, Munich, Germany|Ludwig Maximilians Univ Munchen, Walther Straub Inst Pharmacol & Toxicol, Fac Med, Munich, Germany;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Glass ionomer cement; Zirconia; Nanoparticles; Micro-particles; DNA double-strand breaks;

    机译:玻璃离聚物水泥;氧化锆;纳米颗粒;微粒;DNA双链断裂;
  • 入库时间 2022-08-18 04:13:12

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