在原花青素处理的树脂-牙本质界面上评估胶原蛋白和微渗透性。

B. Aydın, L. Hassan, G. Viana, A. Bedran-Russo
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引用次数: 10

摘要

目的建立一种同时评价化学试剂在树脂-牙本质界面诱导的微渗透性和胶原交联的荧光方法。材料与方法研究了三种化学制剂(富含原花青素的葡萄籽提取物:GSE;盐酸碳二亚胺/ n -羟基琥珀酰亚胺:EDC/NHS;戊二醛(GD)和对照物(蒸馏水)作为底漆,应用于48颗牙齿咬合牙本质的平坦表面,并使用两种市售的蚀刻-冲洗粘合剂进行修复。用罗丹明- b溶液抛光和浸润树脂-牙本质界面,用于共聚焦激光扫描显微镜分析。所选择的参数将允许同时获得胶原蛋白和界面微渗透性(罗丹明- b)。将荧光发射强度(FEI)转换为数字,计算各组的数值。数据采用单因素方差分析、事后Scheffe检验和多重比较检验(α = 0.05)进行统计学分析。使用Pearson相关的t检验来研究胶原交联与微渗透性之间的相关性。结果GD组胶原蛋白的FEI最高,GSE组次之,EDC/ NHS组与对照组差异无统计学意义(p < 0.05)。粘接剂对微渗透性有显著影响(p < 0.05)。GSE组的微渗透性最低,与粘接剂无关(p < 0.001)。微通透性与胶原自身荧光之间存在弱相关性。结论GSE和GD诱导的非酶促胶原交联可通过胶原自身荧光增强检测,并导致界面微通透性降低。胶原自身荧光增强与荧光胶原交联和树脂-牙本质界面微通透性降低有关。胶原蛋白自身荧光是检测自身荧光外源交联及其对树脂-牙本质界面质量的潜在影响的有用工具。
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Assessing Collagen and Micro-permeability at the Proanthocyanidin-treated Resin-Dentin Interface.
PURPOSE To establish a fluorescence-based method to simultaneously assess micro-permeability and collagen cross-linking induced by chemical agents at the resin-dentin interface. MATERIALS AND METHODS Three chemical agents were investigated (proanthocyanidin-rich grape seed extract: GSE; carbodiimide hydrochloride/N-hydroxysuccinimide: EDC/NHS; glutaraldehyde: GD) along with a control (distilled water) as primers applied on flat occlusal dentin surfaces of 48 teeth and restored with two commercially available etch-and-rinse adhesives. Resin-dentin interfaces were polished and infiltrated with rhodamine-B solution for confocal laser scanning microscopy analysis. Parameters were chosen that would allow acquisition of a simultaneous appearance of collagen and interfacial micro-permeability (rhodamine-B). Fluorescence emission intensity (FEI) was converted into numerals and values were calculated for each group. Data were statistically analyzed using one-way ANOVA and post-hoc Scheffe's and multiple comparisons tests (α = 0.05). T-tests with Pearson correlations were used to investigate correlations between collagen cross-linking and micro-permeability. RESULTS The FEI of collagen was the highest for GD, followed by GSE, with no significant differences between EDC/ NHS and the control group (p > 0.05). Micro-permeability was significantly affected by the adhesives (p < 0.05). Micro- permeability was the lowest for GSE groups, regardless of the adhesives (p < 0.001). Weak correlations were found between micro-permeability and collagen auto-fluorescence. CONCLUSIONS Non-enzymatic collagen cross-linking induced by GSE and GD can be detected by increased collagen auto-fluorescence, and results in reduced interfacial micro-permeability. Increased collagen auto-fluorescence was correlated with fluorescent collagen cross-links and decreased micro-permeability at the resin-dentin interface. Collagen auto-fluorescence is a useful tool to detect auto-fluorescent exogenous cross links and their potential impact on the quality of the resin-dentin interface.
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