©Operative Dentistry, 2006, 31-5, 610-615
CSC Pfeifer • RR Braga • JL Ferracane
Clinical RelevanceNew photoactivation protocols need to be tested before being recommended for clinical use. This study suggests that pulse-delay curing may be an efficient way to reduce polymerization shrinkage stress without compromising degree of conversion or polymer network structure.
SUMMARYObjectives: Evaluate the influence of pulse-delay curing on shrinkage stress and microhardness of 2 restorative composites (Herculite XRV and Tetric Ceram). Methods: Two pulse irradiances (500 and 100 mW/cm 2 ) were applied for 1 or 5 seconds, respectively (radiant exposure = 0.5 J/cm 2 ). In both cases, photoactivation was completed applying 500 mW/cm 2 for 39 seconds after a delay time of 0, 1 or 3 minutes. Shrinkage stress was monitored for 10 minutes in specimens 5-mm in diameter by 1-mm in height. Knoop hardness (KHN) was used to estimate the degree of conversion 10 minutes after photoactivation and after 48 hours of storage in distilled water (37°C) in specimens with similar geometry and dimensions. Additional KHN readings after 48 hours of storage in ethanol (37°C) were used to estimate polymer structure. The results were evaluated using ANOVA/Tukey test and Student t-test (α α=0.05). Results: For Tetric Ceram, 3-minute delay led to stress reduction compared to continuous curing at 500 mW/cm 2 (4.7±0.6 MPa and 7.0±1.3 MPa, respectively). At 100 mW/cm 2 , 1 minute delay was enough to cause significant stress reduction (5.2±0.5 MPa). For Herculite, the pulse with 3 minute delay led to stress reduction compared to no delay for both irradiances (100 mW/cm 2 : 6.3±0.5 MPa and 7.8±0.8 MPa, respectively; 500 mW/cm 2 : 6.4±0.3 MPa and 7.8±0.7 MPa, respectively). At 10 minutes, only small differences in microhardness were observed for both materials. No differences were found after water and ethanol storage (p>0.05). Conclusions: The composites behaved differently when subjected to pulse curing. Stress reduction was influenced by delay time but not by pulse irradiance. KHN results suggest that similar degrees of conversion and polymer structure were achieved with the photoactivation methods tested.