Department of Restorative Dentistry, University of Illinois at Chicago, College of Dentistry, Chicago, Illinois 60612, USA.
J Biomed Mater Res B Appl Biomater. 2010 Jul;94(1):250-5. doi: 10.1002/jbm.b.31649.
To characterize the interaction of 1-Ethyl-3-[3-dimethylaminopropyl] carbodiimide Hydrochloride (EDC) with dentin matrix and its effect on the resin-dentin bond.
Changes to the stiffness of demineralized dentin fragments treated with EDC/N-hydroxysuccinimide (NHS) in different solutions were evaluated at different time points. The resistance against enzymatic degradation was indirectly evaluated by ultimate tensile strength (UTS) test of demineralized dentin treated or not with EDC/NHS and subjected to collagenase digestion. Short- and long-term evaluations of the strength of resin-dentin interfaces treated with EDC/NHS for 1 h were performed using microtensile bond strength (microTBS) test. All data (MPa) were individually analyzed using ANOVA and Tukey HSD tests (alpha = 0.05).
The different exposure times significantly increased the stiffness of dentin (p < 0.0001, control-5.15 and EDC/NHS-29.50), while no differences were observed among the different solutions of EDC/NHS (p = 0.063). Collagenase challenge did not affect the UTS values of EDC/NHS group (6.08) (p > 0.05), while complete degradation was observed for the control group (p = 0.0008, control-20.84 and EDC/NHS-43.15). EDC/NHS treatment did not significantly increase resin-dentin muTBS, but the values remained stable after 12 months water storage (p < 0.05).
Biomimetic use of EDC/NHS to induce exogenous collagen cross-links resulted in increased mechanical properties and stability of dentin matrix and dentin-resin interfaces.
研究 1-乙基-3-[3-二甲基氨基丙基]碳化二亚胺盐酸盐(EDC)与牙本质基质的相互作用及其对树脂-牙本质粘结的影响。
在不同溶液中用 EDC/N-羟基琥珀酰亚胺(NHS)处理脱矿牙本质碎片,评估其在不同时间点的硬度变化。通过未用 EDC/NHS 处理和用 EDC/NHS 处理并经胶原酶消化的脱矿牙本质的极限拉伸强度(UTS)试验,间接评估其对酶降解的抵抗力。用微拉伸粘结强度(microTBS)试验对用 EDC/NHS 处理 1 h 的树脂-牙本质界面的短期和长期强度进行评估。所有数据(MPa)均采用方差分析和 Tukey HSD 检验(alpha = 0.05)进行个体分析。
不同的暴露时间显著增加了牙本质的硬度(p < 0.0001,对照组为 5.15,EDC/NHS 组为 29.50),而 EDC/NHS 的不同溶液之间没有差异(p = 0.063)。胶原酶挑战对 EDC/NHS 组的 UTS 值没有影响(6.08)(p > 0.05),而对照组则完全降解(p = 0.0008,对照组为 20.84,EDC/NHS 组为 43.15)。EDC/NHS 处理并没有显著增加树脂-牙本质的 muTBS,但在 12 个月水储存后,其值保持稳定(p < 0.05)。
仿生使用 EDC/NHS 诱导外源性胶原蛋白交联,导致牙本质基质和牙本质-树脂界面的机械性能和稳定性增加。