将掺铜的生物活性玻璃纳米颗粒掺入树脂复合材料中,提高了树脂复合材料的生物性能、力学性能和粘附性能。

Romina Aliaga-Gálvez, Mario Felipe Gutiérrez, Benjamín Valenzuela, Saulo Geraldeli, Gabriel Abuna, Carolina Inostroza, Cristian Bravo, Gabriel Cochinski, Alessandro D Loguercio
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For CTX, the Gingival mesenchymal stem cells (GMSC) cell line was used. For UTS and KHN, specimens were tested after 24 h and 28 days. For bonding evaluation, a universal adhesive was applied on flat dentin surfaces, experimental resin composite build-ups were prepared, and specimens were sectioned to obtain resin-dentin sticks. These were evaluated for μTBS, NL and DC after water storage. Data were submitted to statistical analyses (α = 0.05).</p><p><strong>Results: </strong>The addition of 5% and 10% of BG/CuNp increases AMA (P 0.05), while the CTX remained unchanged with resin-containing BG/CuNp (P > 0.05). UTS and KHN remained stable with the addition of 5% and 10% of BG/CuNp at 24 h, but showed significantly higher values compared to the control after 28 d (P 0.05). μTBS and in-situ DC remained unchanged with BG/CuNp addition, regardless of the concentration added. 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引用次数: 0

摘要

目的:制备和表征掺铜生物活性玻璃纳米颗粒(BG/CuNp),并评价其加入树脂复合材料对抗菌活性(AMA)、细胞毒性(CTX)、极限抗拉强度(UTS)、Knoop显微硬度(KHN)、树脂-牙本质直接微拉伸结合强度(μTBS)、纳米渗漏(NL)和原位转化率(DC)的影响。材料和方法:在树脂复合材料中加入不同浓度的BG/CuNp(0%[对照];5、10和20 wt%)。对AMA进行了抗变形链球菌的评价。CTX采用牙龈间充质干细胞(GMSC)细胞系。UTS和KHN分别在24 h和28 d后进行检测。为了评估粘接,在牙本质平面上应用通用粘合剂,制备实验树脂复合材料,并对标本进行切片以获得树脂-牙本质棒。分别测定贮藏后的μTBS、NL和DC。数据进行统计学分析(α = 0.05)。结果:添加5%和10% BG/CuNp可使AMA增加(P < 0.05),而含树脂BG/CuNp组CTX不变(P < 0.05)。添加5%和10% BG/CuNp时,24 h UTS和KHN保持稳定,但28 d后显著高于对照组(p0.05)。无论添加BG/CuNp的浓度如何,μTBS和原位DC均保持不变。而BG/CuNp组NL显著降低(p0.05)。结论:在树脂复合材料中加入实验浓度的BG/CuNp可能是一种提供抗菌活性和改善杂化层完整性的替代方法,同时不影响生物、粘合和机械性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Incorporation of Copper-Doped Bioactive Glass Nanoparticles into Resin Composites Improves Their Biological, Mechanical and Adhesive Properties.

Purpose: This study aims to develop and characterize copper-doped bioactive glass nanoparticles (BG/CuNp), and to evaluate the effects of their addition into a resin composite on antimicrobial activity (AMA), cytotoxicity (CTX), ultimate tensile strength (UTS), Knoop microhardness (KHN), as well as immediate resin-dentin microtensile bond strength (μTBS), nanoleakage (NL) and in-situ degree of conversion (DC).

Materials and methods: BG/CuNp were added to a resin composite at different concentrations (0% [control]; 5, 10 and 20 wt%). The AMA was evaluated against Streptococcus mutans. For CTX, the Gingival mesenchymal stem cells (GMSC) cell line was used. For UTS and KHN, specimens were tested after 24 h and 28 days. For bonding evaluation, a universal adhesive was applied on flat dentin surfaces, experimental resin composite build-ups were prepared, and specimens were sectioned to obtain resin-dentin sticks. These were evaluated for μTBS, NL and DC after water storage. Data were submitted to statistical analyses (α = 0.05).

Results: The addition of 5% and 10% of BG/CuNp increases AMA (P 0.05), while the CTX remained unchanged with resin-containing BG/CuNp (P > 0.05). UTS and KHN remained stable with the addition of 5% and 10% of BG/CuNp at 24 h, but showed significantly higher values compared to the control after 28 d (P 0.05). μTBS and in-situ DC remained unchanged with BG/CuNp addition, regardless of the concentration added. However, significantly lower NL was observed for BG/CuNp groups (P 0.05).

Conclusion: The addition of BG/CuNp in the tested concentrations into a resin composite may be an alternative to provide antimicrobial activity and improve the integrity of the hybrid layer, without compromising biological, adhesives and mechanical properties.

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