Rueggeberg F A, Caughman W F, Chan D C
Dental Materials Section, Medical College of Georgia, Augusta, USA.
J Esthet Dent. 1999;11(4):197-205. doi: 10.1111/j.1708-8240.1999.tb00399.x.
The objective of this research was to evaluate a novel approach to monitor the polymerization reaction during a light-curing exposure by using infrared (IR) spectroscopy.
An IR spectrometer was equipped to use an attenuated total reflectance (ATR) element as an IR-active substrate. The uncured composite (Herculite XRV, Shade A2, Kerr, Orange, California) was placed against the crystal, and the IR spectrum was continuously obtained during various exposure scenarios. The degree of conversion and the maximum rate of reaction were monitored at 0 mm (top surface), 1 mm, 2 mm, and 3 mm beneath the surface. The exposure conditions included continuous 40-second or 60-second exposures at 100% intensity (800 mW/cm2) or a stepped output of 10 seconds at 17% maximal output (133 mW/cm2) followed by full output for the remainder of the 40-second or 60-second exposure (Elipar Highlight, ESPE, Norristown Pennsylvania). The results were analyzed using MANOVA with appropriate post hoc tests (p < or = .05).
For 40-second exposures, the peak conversion rates were significantly reduced (p < .05) when using the stepped exposure mode compared to the continuous exposure: 40-second top surface: stepped = 5.5%/s +/- 0.4, continuous = 10.5%/s +/- 1.0; 1 mm step = 3.6%/s +/- 0.4, continuous mode = 4.8%/s +/- 0.2. The same trend was noted when using the 60-second exposure. Equivalent conversion values (p > .05) beneath the surface between stepped and continuous exposure modes at similar depths 60 seconds after light initiation were only attained at 3 mm 4 for the 40-second exposure. However, using the 60-second exposure, equivalent conversion values between step and continuous exposure modes at similar depths were obtained. Even with a reduced conversion rate at the surface using the stepped cure mode, polymerization shrinkage forces were sufficient to debond the specimens from the test crystal after only 20 seconds into the exposure. This result indicated that stress development in the curing composite was non-uniform, and stress values developed at the surface of the restoration were the greatest.
Stepped intensity curing for the ESPE Highlight unit was shown to produce significantly lower conversion rates at the surface and at 1-mm depths, but longer exposure times were still required to provide conversion values equivalent to continuous exposure.
本研究的目的是评估一种通过红外(IR)光谱监测光固化暴露过程中聚合反应的新方法。
配备一台红外光谱仪,使用衰减全反射(ATR)元件作为红外活性底物。将未固化的复合材料(Herculite XRV,A2色,Kerr公司,加利福尼亚州奥兰治)放置在晶体上,并在各种暴露场景下连续获取红外光谱。在表面以下0毫米(顶面)、1毫米、2毫米和3毫米处监测转化率和最大反应速率。暴露条件包括在100%强度(800 mW/cm²)下连续40秒或60秒暴露,或在17%最大输出(133 mW/cm²)下进行10秒的阶梯输出,随后在40秒或60秒暴露的剩余时间内进行全输出(Elipar Highlight,ESPE公司,宾夕法尼亚州诺里斯敦)。使用多变量方差分析(MANOVA)和适当的事后检验(p≤0.05)对结果进行分析。
对于40秒的暴露,与连续暴露相比,使用阶梯暴露模式时峰值转化率显著降低(p<0.05):40秒顶面:阶梯式=5.5%/秒±0.4,连续式=10.5%/秒±1.0;1毫米处阶梯式=3.6%/秒±0.4,连续模式=4.8%/秒±0.2。使用60秒暴露时也观察到相同趋势。在光起始60秒后,在相似深度下,阶梯式和连续暴露模式在表面以下仅在3毫米处达到等效转化率值(p>0.05)。然而,使用60秒暴露时,在相似深度下获得了阶梯式和连续暴露模式之间的等效转化率值。即使在使用阶梯固化模式时表面转化率降低,但仅在暴露20秒后,聚合收缩力就足以使试样从测试晶体上脱粘。该结果表明固化复合材料中的应力发展不均匀,修复体表面产生的应力值最大。
对于ESPE Highlight装置,阶梯强度固化在表面和1毫米深度处显示出显著较低的转化率,但仍需要更长的暴露时间以提供与连续暴露等效的转化率值。