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不锈钢和镍钛正畸合金释放离子的表征及细胞毒性

Characterization and cytotoxicity of ions released from stainless steel and nickel-titanium orthodontic alloys.

作者信息

Eliades Theodore, Pratsinis Harris, Kletsas Dimitris, Eliades George, Makou Margarita

机构信息

Biomaterials Laboratory, School of Dentistry, University of Athens, Greece.

出版信息

Am J Orthod Dentofacial Orthop. 2004 Jan;125(1):24-9. doi: 10.1016/j.ajodo.2003.09.009.

Abstract

The purpose of this study was to qualitatively and quantitatively characterize the substances released from orthodontic brackets and nickel-titanium wires and to comparatively assess the cytotoxicity of the ions released from these orthodontic alloys. Two full sets of stainless steel brackets of 20 brackets each (weight 2.1 g) and 2 groups of 0.018 x 0.025 Ni-Ti archwires of 10 wires each (weight 2.0 g) were immersed in 0.9% saline solution for a month. The immersion media were analyzed with inductively coupled plasma-atomic emission spectroscopy (ICP-AES), and the ionic content was statistically analyzed with 1-way analysis of variance (ANOVA). Human periodontal ligament fibroblasts and gingival fibroblasts were exposed to various concentrations of the 2 immersion media; nickel chloride was used as a positive control for comparison purposes. The cytotoxic or cytostatic activity of the media was investigated with the MTT and the DNA synthesis assays. The results of the cytotoxicity assay were analyzed with 2-way ANOVA and the Tukey test with solution and concentration variants as discriminating variables (alpha=0.05). The results indicated no ionic release for the nickel-titanium alloy aging solution, whereas measurable nickel and traces of chromium were found in the stainless steel bracket-aging medium. Concentrations of the nickel chloride solution greater then 2 mM were found to reduce by more than 50% the viability and DNA synthesis of fibroblasts; however, neither orthodontic materials-derived media had any effect on the survival and DNA synthesis of either cells.

摘要

本研究的目的是对从正畸托槽和镍钛丝中释放的物质进行定性和定量表征,并比较评估这些正畸合金释放离子的细胞毒性。将两套完整的不锈钢托槽(每套20个托槽,重量2.1 g)和两组每组10根的0.018×0.025镍钛弓丝(重量2.0 g)浸泡在0.9%的盐溶液中一个月。用感应耦合等离子体原子发射光谱法(ICP-AES)分析浸泡介质,并采用单因素方差分析(ANOVA)对离子含量进行统计分析。将人牙周膜成纤维细胞和牙龈成纤维细胞暴露于两种浸泡介质的不同浓度中;使用氯化镍作为阳性对照以作比较。用MTT和DNA合成试验研究介质的细胞毒性或细胞生长抑制活性。细胞毒性试验结果采用双因素方差分析和Tukey检验进行分析,以溶液和浓度变量作为判别变量(α=0.05)。结果表明,镍钛合金老化溶液无离子释放,而在不锈钢托槽老化介质中发现了可测量的镍和微量铬。发现氯化镍溶液浓度大于2 mM时,成纤维细胞的活力和DNA合成降低了50%以上;然而,两种正畸材料衍生的介质对两种细胞的存活和DNA合成均无任何影响。

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