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市售大体积充填复合材料的深度修复质量:逐层机械和生物学评价。

Quality of Cure in Depth of Commercially Available Bulk-fill Composites: A Layer-by-layer Mechanical and Biological Evaluation.

机构信息

*Matthieu Gilli, Adult and Child Dentistry, Cliniques Universitaires Saint-Luc, Brussels, Belgium; DRIM Research Group & Advanced Drug Delivery and Biomaterials, Louvain Drug Research Institute, UCLouvain, Brussels, Belgium.

Thibaut G Hollaert, Adult and Child Dentistry, Cliniques Universitaires Saint-Luc, Brussels, Belgium; DRIM Research Group & Advanced Drug Delivery and Biomaterials, Louvain Drug Research Institute, UCLouvain, Brussels, Belgium.

出版信息

Oper Dent. 2022 Jul 1;47(4):437-448. doi: 10.2341/21-084-L.

DOI:10.2341/21-084-L
PMID:35917249
Abstract

Despite their popularity, the use of bulk-fill composites remains controversial, both in terms of their properties and their in-depth development. The objectives of the present work were (1) to provide a more comprehensive evaluation of the quality of cure in depth of commercially available bulk-fill composites by combining various key mechanical and biological characterization methods, (2) to evaluate the inter-material differences when optimally cured, and (3) to evaluate the efficiency of an antioxidant-N-acetyl-cysteine (NAC)-to restrain the adverse effects of the leached components on cell viability. Nine bulk-fill composites (including flowable and high-viscosity materials) were investigated and compared to two conventional resin-based composites, one flowable and one high-viscosity restorative material. The materials were injected or packed into Teflon molds of various configurations, up to 6 mm material thickness. They were then light-cured from the top for 20 seconds with Bluephase G2 (Ivoclar Vivadent, irradiance = 1050 mW/cm2). The following physico-mechanical properties were measured for the upper (0-2 mm), intermediate (2-4 mm), and lower (4-6 mm) layers: degree of conversion using Raman Spectrometry (DC, in %), microhardness using a Vickers micro-indenter before (VHN dry) and after 24 hours of storage in ethanol (VHN EtOH), and flexural strength (in MPa) and flexural modulus (in GPa) using a three-point bend test. Each composite layer and an uncured layer were also stored for one week in a standard cell growth medium to generate conditioned media. Human dental pulp cells were then cultured for 24 hours with the latter and cell viability was measured using an MTS assay. A similar experiment was repeated with conditioned media produced in contact with uncured composites, with and without the addition of 4 mM NAC. The data were subjected to a Shapiro-Wilk test, then one-way ANOVA or Kruskal-Wallis test, followed either by Tukey's test (inter-material comparison) or by Dunnett's or Dunn's test (comparison between layers relative to the upper one). The level of statistical significance was set at 0.05. Some materials (EverX, X-traF, VenusBF, X-traB) did not show any significant differences (p>0.05) for any of the properties considered between the intermediate layers compared to the upper one (considered as reference). Others displayed significant differences, at least for some properties, highlighting the value of combining various key mechanical and biological characterization methods when investigating the quality of cure in depth. Significant inter-material differences (p<0.05) were observed when comparing the properties of their upper layer, considered as "optimally" polymerized. Hence, one needs to consider the absolute property values, not only their relative evolution concerning layer thickness. Finally, the use of NAC appeared as beneficial to reduce the risk of harmful effects to dental pulp cells, especially in case of excessive thickness use, and may therefore be of potential interest as an additive to composites in the future.

摘要

尽管它们很受欢迎,但在深入研究其性能和特性方面,大量填充复合材料的使用仍然存在争议。本研究的目的是:(1)通过结合各种关键的机械和生物学特性评估方法,更全面地评估市售大量填充复合材料的固化质量;(2)评估优化固化时的材料间差异;(3)评估抗氧化剂 N-乙酰半胱氨酸(NAC)的效率,以抑制浸出成分对细胞活力的不利影响。研究了 9 种大量填充复合材料(包括流动和高粘度材料),并将其与两种传统的树脂基复合材料、一种流动和一种高粘度修复材料进行了比较。将材料注入或填充到各种配置的特氟龙模具中,厚度可达 6 毫米。然后用 Bluephase G2(Ivoclar Vivadent,辐照度=1050 mW/cm2)从顶部进行 20 秒的光固化。对于上(0-2 毫米)、中(2-4 毫米)和下(4-6 毫米)层,分别测量了以下物理力学性能:拉曼光谱法(DC)测量的转化率(%)、用维氏硬度计在 24 小时乙醇储存前(VHN 干燥)和后(VHN EtOH)测量的显微硬度值、用三点弯曲试验测量的弯曲强度(MPa)和弯曲模量(GPa)。每层复合材料和未固化层还在标准细胞生长培养基中储存一周,以生成条件培养基。然后用人牙髓细胞培养 24 小时,并用 MTS 测定法测量细胞活力。用相同的实验重复接触未固化复合材料产生的条件培养基,同时添加和不添加 4mM NAC。对数据进行 Shapiro-Wilk 检验,然后进行单因素方差分析或 Kruskal-Wallis 检验,然后进行 Tukey 检验(材料间比较)或 Dunnett 或 Dunn 检验(与上层比较的层间比较)。统计显著性水平设为 0.05。一些材料(EverX、X-traF、VenusBF、X-traB)在上层(作为参考)与中层之间的任何考虑的性能之间没有显示出任何显著差异(p>0.05)。其他材料则至少在某些性能上显示出显著差异,这突出了在深入研究固化质量时,结合各种关键机械和生物学特性评估方法的重要性。当比较其上层(被认为是“最佳”聚合的)的性能时,观察到显著的材料间差异(p<0.05)。因此,需要考虑绝对的性能值,而不仅仅是它们相对于层厚度的相对变化。最后,使用 NAC 似乎可以降低对牙髓细胞有害影响的风险,尤其是在过度使用厚度的情况下,因此将来可能作为复合材料的添加剂具有潜在的意义。

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