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纳米和微米二氧化硅对传统玻璃离子水门汀凝固时间和显微硬度的影响

The Impact of Nano- and Micro-Silica on the Setting Time and Microhardness of Conventional Glass-Ionomer Cements.

作者信息

Güçlü Zeynep A, Patat Şaban, Coleman Nichola J

机构信息

Department of Pediatric Dentistry, Faculty of Dentistry, Erciyes University, Melikgazi, Kayseri 38039, Türkiye.

ERNAM, Erciyes University Nanotechnology Application & Research Center, Erciyes University, Melikgazi, Kayseri 38039, Türkiye.

出版信息

Dent J (Basel). 2024 Feb 27;12(3):54. doi: 10.3390/dj12030054.

Abstract

The objective of this study was to investigate the effect of the incorporation of 2, 4 or 6 wt% of amorphous nano- or micro-silica (Aerosil OX 50 or Aeroperl 300 Pharma (Evonik Operations GmbH, Essen, Germany), respectively) on the net setting time and microhardness of Ketac™ Molar (3M ESPE, St. Paul, MN, USA) and Fuji IX GP (GC Corporation, Tokyo, Japan) glass-ionomer cements (GICs) (viz. KM and FIX, respectively). Both silica particles were found to cause a non-linear, dose-dependent reduction in setting time that was within the clinically acceptable limits specified in the relevant international standard (ISO 9917-1:2007). The microhardness of KM was statistically unaffected by blending with 2 or 4 wt% nano-silica at all times, whereas 6 wt% addition decreased and increased the surface hardness at 1 and 21 days, respectively. The incorporation of 4 or 6 wt% nano-silica significantly improved the microhardness of FIX at 1, 14 and 21 days, with no change in this property noted for 2 wt% addition. Micro-silica also tended to enhance the microhardness of FIX, at all concentrations and times, to an extent that became statistically significant for all dosages at 21 days. Conversely, 4 and 6 wt% additions of micro-silica markedly decreased the initial 1-day microhardness of KM, and the 21-day sample blended at 4 wt% was the only specimen that demonstrated a significant increase in this property. Scanning electron microscopy indicated that the nano- and micro-silica particles were well distributed throughout the composite structures of both GICs with no evidence of aggregation or zoning. The specific mechanisms of the interaction of inorganic nanoparticles with the constituents of GICs require further understanding, and a lack of international standardization of the determination of microhardness is problematic in this respect.

摘要

本研究的目的是调查分别掺入2%、4%或6%重量比的无定形纳米或微米二氧化硅(分别为Aerosil OX 50或Aeroperl 300 Pharma(赢创工业运营有限公司,埃森,德国))对Ketac™ Molar(3M ESPE,圣保罗,明尼苏达州,美国)和Fuji IX GP(GC公司,东京,日本)玻璃离子水门汀(GICs)(分别即KM和FIX)的净凝固时间和显微硬度的影响。发现两种二氧化硅颗粒均会导致凝固时间呈非线性、剂量依赖性降低,且该降低幅度在相关国际标准(ISO 9917-1:2007)规定的临床可接受范围内。在所有时间点,与2%或4%重量比的纳米二氧化硅混合后,KM的显微硬度在统计学上均无变化,而添加6%重量比的纳米二氧化硅分别在1天和21天时降低和增加了表面硬度。掺入4%或6%重量比的纳米二氧化硅在1天、14天和21天时显著提高了FIX的显微硬度,添加2%重量比时该性能无变化。微米二氧化硅在所有浓度和时间下也倾向于提高FIX的显微硬度,在21天时所有剂量的提高幅度均具有统计学意义。相反,添加4%和6%重量比的微米二氧化硅显著降低了KM最初1天的显微硬度,4%重量比混合的21天样本是唯一显示该性能显著增加的样本。扫描电子显微镜表明,纳米和微米二氧化硅颗粒在两种GICs的复合结构中分布良好,没有聚集或分区的迹象。无机纳米颗粒与GICs成分相互作用的具体机制需要进一步了解,在这方面,显微硬度测定缺乏国际标准化是个问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47f2/10968912/29b6f4d24c3e/dentistry-12-00054-g001.jpg

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