Ilie Nicoleta
Department of Conservative Dentistry and Periodontology, University Hospital, LMU Munich, Goethestr 70, 80336 Munich, Germany.
Materials (Basel). 2018 Jan 11;11(1):108. doi: 10.3390/ma11010108.
Dental bulk-fill restorations with resin-composites (RBC) are increasing in popularity, but doubts concerning insufficient curing in depth still disconcert clinicians. An alternative might be offered by modern dual-cured RBCs, which additionally provide bioactive properties. This study assessed the impact of additional light-curing on polymerization kinetics, the degree of conversion (DC) and mechanical properties of a novel, dual-cured RBC with alkaline fillers. Since the bioactivity of a material often implies a release of compounds, the mechanical stability in simulated clinical environments was also evaluated. Polymerization kinetics and DC were assessed at 2- and 4-mm specimen depths in real-time up to one hour ( = 6). Incident and transmitted irradiance and radiant exposure were recorded at 2- and 4-mm depths. Micro-mechanical profiles ( = 6) were assessed in 100-µm steps along 6-mm deep specimens at 24 h post-polymerization. Flexural strength and modulus ( = 10) were determined up to three months of immersion in neutral (6.8) and acidic (4) pH conditions. DC variation in time was best described by a sigmoidal function (R² > 0.98), revealing a retarded (3.4 ± 0.4 min) initiation in C=C double bond conversion in self-cured versus dual-cured specimens. The setting reaction kinetic was identical at 2- and 4-mm depths for the self-cure mode. For the dual-cure mode, polymerization initiated at 2-mm depth instantly with light-irradiation, while being retarded (0.8 min) at 4-mm depth. The material behaves similarly, irrespective of curing mode or depth, later than 11 min after mixing. Flexural strength and modulus was comparable to regular RBCs and maintained up to three months in both neutral and acidic conditions. Additional light-curing initially accelerates the polymerization kinetic and might help shorten the restauration procedure by hardening the material on demand, however with no effect on the final properties.
树脂复合材料(RBC)的牙科大块充填修复越来越受欢迎,但对于深层固化不足的疑虑仍困扰着临床医生。现代双固化RBC可能是一种替代方案,它还具有生物活性。本研究评估了额外光固化对一种新型含碱性填料的双固化RBC的聚合动力学、转化率(DC)和机械性能的影响。由于材料的生物活性通常意味着化合物的释放,因此还评估了其在模拟临床环境中的机械稳定性。在长达一小时(=6)的时间内,实时评估2毫米和4毫米试样深度处的聚合动力学和DC。记录2毫米和4毫米深度处的入射和透射辐照度以及辐射暴露量。在聚合后24小时,沿着6毫米深的试样以100微米步长评估微观力学轮廓(=6)。在中性(6.8)和酸性(4)pH条件下浸泡长达三个月,测定弯曲强度和模量(=10)。DC随时间的变化最好用S形函数描述(R²>0.98),表明自固化与双固化试样中C=C双键转化的起始延迟(3.4±0.4分钟)。自固化模式下,2毫米和4毫米深度处的固化反应动力学相同。对于双固化模式,2毫米深度处光照后立即引发聚合,而4毫米深度处延迟(0.8分钟)。混合后11分钟后,无论固化模式或深度如何,材料表现相似。弯曲强度和模量与常规RBC相当,在中性和酸性条件下均能保持三个月。额外的光固化最初会加速聚合动力学,可能有助于通过按需硬化材料来缩短修复过程,但对最终性能没有影响。