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在同时进行聚合和溶剂损失过程中牙科粘合剂的衰减全反射傅里叶变换红外光谱解析

Interpretation of ATR-FTIR spectra of dental adhesives throughout simultaneous polymerization and solvent loss.

作者信息

Almusa Arwa, Delgado António H S, Young Anne Margaret

机构信息

Division of Biomaterials and Tissue Engineering, UCL Eastman Dental Institute, London, United Kingdom.

Department of Restorative Dental Science, College of Dentistry, King Saud University, Riyadh, Saudi Arabia.

出版信息

PLoS One. 2025 Jun 11;20(6):e0325692. doi: 10.1371/journal.pone.0325692. eCollection 2025.

Abstract

This study developed new Fourier transform infrared (FTIR) spectroscopy methods to assess effects of drying level on the composition and polymerization kinetics of One-Step® (OS), OptibondTM Universal (OU) and G-Bond (GB) dental adhesives. 5 μL of each adhesive were placed in turn on an FTIR, Attenuated Total Reflectance (ATR) accessory, operating at 37ºC. Spectra were generated before, during and after light-curing (20 s, 1000 mW/cm2, 450-470 nm) at 10 s after placement or following 300 s of passive drying (n = 3). Individual spectra of solvents, monomers and fillers, combined with spectral change upon polymerization, were used to generate model spectra and quantify component levels versus time up to 300 s after start of light exposure. Polymerization rates and maximum degree of conversion were derived using a combination of polymer and monomer peaks at 1480 and 1320 cm-1. Inferential analyses included Kruskal-Wallis/Mann-Whitney U using a significance level of 5%. Initial acetone levels were 65, 48 and 50% in OS, OU and GB, respectively, whilst curing at 10 versus 300 s gave final acetone levels of 35, 20 and 32% versus 0, 0 and 10%. With earlier light exposure, monomer reaction rate was reduced but continued for longer leading to final conversions of 88, 86 and 40% versus 61, 66 and 77% for OS, OU and GB, respectively. The FTIR techniques developed could monitor process kinetics and demonstrate the large, highly significant effects of drying method on final polymerized dental adhesive composition and polymerization level.

摘要

本研究开发了新的傅里叶变换红外(FTIR)光谱法,以评估干燥程度对单步®(OS)、OptibondTM通用型(OU)和G-Bond(GB)牙科粘合剂的成分及聚合动力学的影响。将每种粘合剂5μL依次置于37ºC下运行的FTIR衰减全反射(ATR)附件上。在放置后10秒或被动干燥300秒(n = 3)后,在光固化(20秒,1000 mW/cm2,450 - 470nm)之前、期间和之后生成光谱。溶剂、单体和填料的单个光谱,结合聚合时的光谱变化,用于生成模型光谱并量化光照开始后300秒内各成分水平随时间的变化。使用1480和1320 cm-1处聚合物和单体峰的组合得出聚合速率和最大转化率。推断性分析包括使用5%显著性水平的Kruskal-Wallis/Mann-Whitney U检验。OS、OU和GB中初始丙酮水平分别为65%、48%和50%,而在10秒与300秒固化时,最终丙酮水平分别为35%、20%和32%,与之相比,分别为0%、0%和10%。更早进行光照时,单体反应速率降低,但持续时间更长,导致OS、OU和GB的最终转化率分别为88%、86%和40%,与之相比,分别为61%、66%和77%。所开发的FTIR技术可监测过程动力学,并证明干燥方法对最终聚合牙科粘合剂成分和聚合水平有巨大且高度显著的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f51/12157115/aac3cc25d91b/pone.0325692.g001.jpg

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