Department of Dental Clinical Sciences, Dalhousie University, Halifax, Nova Scotia, B3H 4R2, Canada.
Department of Physics and Atmospheric Science, Dalhousie University, Halifax, Nova Scotia, B3H 4R2, Canada.
J Mech Behav Biomed Mater. 2021 Dec;124:104884. doi: 10.1016/j.jmbbm.2021.104884. Epub 2021 Oct 7.
This study: 1) aims to measure with high temporal resolution the intrinsic rate of the degree of conversion (DC) of a dental resin-based composite (RBC) photo-cured at two irradiances; 2) aims to determine the transition time at which the DC rate is maximum; 3) used two different irradiances to measure the shift in transition time; 4) aims to compare transition times measured using DC and shrinkage strain.
Samples (n = 20) 1 mm thick by 10 mm diameter of Filtek One bulk-fill restorative A2 shade (3M Oral Care) were photocured for 20 s with a single emission peak (wavelength centered at 455 nm) light-emitting-diode-based light-curing unit at irradiance levels of 890 mW/cm and 209 mW/cm, and initial sample temperature of T = 23 °C. The DC was measured in real-time using Attenuated Total Reflection (ATR) FTIR spectroscopy with a sampling rate of 13 DC data points per second. The data were analyzed within a phenomenological autocatalytic model. In addition, the axial shrinkage strain was measured using 3 samples of the RBC with the same outer dimensions and under similar experimental conditions using the bonded disk method and an interferometric technique.
For the 890 mW/cm and 209 mW/cm irradiance levels, the DC with time was found to agree with the model enabling the determination of transition times of 0.66 ± 0.05 s and 2.3 ± 0.2 s, and the DC at these times of 5.5 ± 0.2% and 6.4 ± 0.2%. The maximum linear strain rate at 0.76 ± 0.01 s and 1.98 ± 0.02 s for the 890 mW/cm and 209 mW/cm irradiance levels, respectively, are within two standard deviations of the corresponding transition times.
At an irradiance level much greater than 1000 mW/cm, the photo-polymerization kinetics of a dental RBC may be too fast to be measured accurately using ATR-FTIR spectroscopy. A viable alternative to monitor the kinetics is through the measurements of the axial shrinkage strain employing the bonded disk method and an interferometric technique.
本研究:1)旨在以高时间分辨率测量两种辐照度下光固化牙科树脂基复合材料(RBC)的转化率(DC)的固有速率;2)旨在确定 DC 速率最大的转变时间;3)使用两种不同的辐照度来测量转变时间的偏移;4)旨在比较使用 DC 和收缩应变测量的转变时间。
采用 Filtek One 块状填充修复剂 A2 色(3M 口腔护理),厚度为 1mm,直径为 10mm,在初始样品温度为 T=23°C 的情况下,用单个发射峰(波长中心在 455nm)的发光二极管基光固化单元,以 890mW/cm 和 209mW/cm 的辐照度水平对样本进行 20s 的光固化。采用衰减全反射(ATR)傅里叶变换红外光谱法实时测量 DC,采样率为每秒 13 个 DC 数据点。数据在一个唯象自催化模型内进行分析。此外,采用相同的外尺寸和类似的实验条件下的 3 个 RBC 样本,使用粘结盘法和干涉技术测量轴向收缩应变。
对于 890mW/cm 和 209mW/cm 的辐照度水平,随着时间的推移,DC 与模型一致,从而确定了 0.66±0.05s 和 2.3±0.2s 的转变时间,以及在这些时间下的 5.5±0.2%和 6.4±0.2%的 DC。对于 890mW/cm 和 209mW/cm 的辐照度水平,在 0.76±0.01s 和 1.98±0.02s 时的最大线性应变率分别在相应转变时间的两个标准差范围内。
在辐照度远大于 1000mW/cm 的情况下,牙科 RBC 的光聚合动力学可能太快,无法使用 ATR-FTIR 光谱法进行准确测量。一种可行的替代方法是通过使用粘结盘法和干涉技术测量轴向收缩应变来监测动力学。