Giray F E, Peker S, Durmus B, Kargül B
Department of Paediatric Dentistry, School of Dentistry, Marmara University, Istanbul, Turkey.
Eur J Paediatr Dent. 2014 Jun;15(2):122-6.
The aim of this in vitro study was to evaluate the microleakage of the new glass ionomers ChemFil Rock and IonoluxAC in comparison to Fuji IX GP Extra and the composite Aelite LS Posterior in permanent teeth.
Class V standardised U-shaped cavities were made on a total of 40 freshly extracted teeth and restored with different glass ionomer materials (4 groups of 10 samples each). After thermocycling, the teeth were immersed in 0.5% basic fuchsin for 24h. They were then sectioned in the buccolingual direction. Microleakage was assessed for the occlusal and gingival margins under a microscope at 40x magnification.
There were significant differences among the materials used (p=0.000). While there was no dye penetration in the Fuji IX GP EXTRA group, which behaved similarly to the composite resin group, ChemFil Rock showed less microleakage than Ionolux AC. The Wilcoxon rank test showed no significant differences in the occlusal and gingival scores between the groups (p>0.05).
Although cavities filled with a conventional glass ionomer (Fuji IX GP Extra) had significantly less leakage than cavities filled with the new glass ionomers (ChemFil Rock and Ionolux AC), these results do not reflect all the variables present in vivo conditions. As the in vitro evaluation of new materials does not always reveal their full limitations or possibilities, clinical testing of new systems remains the ultimate proof of effectiveness.
本体外研究旨在评估新型玻璃离子水门汀ChemFil Rock和IonoluxAC与Fuji IX GP Extra以及复合树脂Aelite LS Posterior在恒牙中的微渗漏情况。
在总共40颗新鲜拔除的牙齿上制备V类标准化U形洞,并使用不同的玻璃离子材料进行修复(每组10个样本,共4组)。热循环后,将牙齿浸泡在0.5%碱性品红中24小时。然后沿颊舌方向进行切片。在40倍放大倍数的显微镜下评估咬合面和牙龈边缘的微渗漏情况。
所用材料之间存在显著差异(p = 0.000)。Fuji IX GP EXTRA组与复合树脂组表现相似,无染料渗透,而ChemFil Rock的微渗漏比Ionolux AC少。Wilcoxon秩和检验显示各组间咬合面和牙龈评分无显著差异(p>0.05)。
尽管填充传统玻璃离子水门汀(Fuji IX GP Extra)的洞的渗漏明显少于填充新型玻璃离子水门汀(ChemFil Rock和Ionolux AC)的洞,但这些结果并未反映体内条件下的所有变量。由于对新材料的体外评估并不总能揭示其全部局限性或可能性,新系统的临床试验仍然是有效性的最终证明。