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用于永久修复的增材制造和减材制造树脂的单体洗脱

Monomer Elution of Additive- and Subtractive-Manufacturing Resins for Permanent Restorations.

作者信息

Atasoy Samet, Karademir Sultan Aktuğ

出版信息

Int J Prosthodont. 2025 Jul 22;38(4):430-436. doi: 10.11607/ijp.9119.

Abstract

PURPOSE

To evaluate the elution of residual monomers from resins used in additively and subtractively manufactured permanent restorations over a period of 1 month, using high performance liquid chromatography (HPLC).

MATERIALS AND METHODS

Two additive manufacturing permanent crown resins (Crowntec [CT] and VarseoSmile Crown Plus [VS]) and a subtractive-manufacturing resin nanoceramic (Cerasmart [CS]) were used to fabricate 30 disc-shaped samples (10 × 2 mm; n = 10). The elution of bisphenol A ethoxylate dimethacrylate (BisEMA), urethane dimethacrylate (UDMA), and triethylene glycol dimethacrylate (TEGDMA) monomers was measured with HPLC at 1 day and 30 days after immersion. One-way ANOVA and post-hoc Tukey tests were used to evaluate differences in eluted monomer concentrations. Paired-sample t tests were used to test the differences in monomer concentration between storage times.

RESULTS

CS released BisEMA and UDMA residual monomers, while VS and CT released BisEMA and TEGDMA residual monomers. The residual monomer elution from CT was consistently lower than that from VS for both BisEMA (P < .001) and TEGDMA (P < .001). CS showed a decreasing release pattern in BisEMA (P = .002) and UDMA (P < .001) residual monomers, whereas VS and CT showed an increasing release pattern in BisEMA (P < .001) and TEGDMA (P < .001) residual monomers.

CONCLUSIONS

The additive-manufacturing composite resins released higher amounts of residual monomers than the subtractive-manufacturing resin nanoceramic. Although the amounts of residual monomers released in the additive manufacturing composite resins increased over time in contrast to the subtractive manufacturing resin nanoceramic, these values were below cytotoxic levels.

摘要

目的

使用高效液相色谱法(HPLC)评估在1个月的时间内,增材制造和减材制造的永久性修复体所用树脂中残留单体的洗脱情况。

材料与方法

使用两种增材制造永久性全冠树脂(Crowntec [CT]和VarseoSmile Crown Plus [VS])以及一种减材制造树脂纳米陶瓷(Cerasmart [CS])制作30个圆盘形样本(10×2毫米;n = 10)。在浸泡1天和30天后,用HPLC测量双酚A乙氧基二甲基丙烯酸酯(BisEMA)、聚氨酯二甲基丙烯酸酯(UDMA)和三乙二醇二甲基丙烯酸酯(TEGDMA)单体的洗脱情况。采用单因素方差分析和事后Tukey检验评估洗脱单体浓度的差异。使用配对样本t检验来测试储存时间之间单体浓度的差异。

结果

CS释放出BisEMA和UDMA残留单体,而VS和CT释放出BisEMA和TEGDMA残留单体。对于BisEMA(P < .001)和TEGDMA(P < .001),CT的残留单体洗脱量始终低于VS。CS在BisEMA(P = .002)和UDMA(P < .001)残留单体中呈现出释放量减少的模式,而VS和CT在BisEMA(P < .001)和TEGDMA(P < .001)残留单体中呈现出释放量增加的模式。

结论

增材制造复合树脂释放的残留单体量高于减材制造树脂纳米陶瓷。尽管与减材制造树脂纳米陶瓷相比,增材制造复合树脂中释放的残留单体量随时间增加,但这些值低于细胞毒性水平。

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