Oregon Health & Science University, Portland, OR, USA; Piracicaba Dental School, University of Campinas, Piracicaba, SP, Brazil.
Oregon Health & Science University, Portland, OR, USA.
Dent Mater. 2024 Jun;40(6):993-1001. doi: 10.1016/j.dental.2024.05.002. Epub 2024 May 10.
Acrylamides were shown to significantly improve bonding stability in adhesive restorations, but the reinforcement mechanism has not been fully elucidated. We tested the hypothesis that hydrogen bonding reinforcement of the collagen network (with secondary or tertiary acrylamides), as well as degree of crosslinking of the polymer network (with di- or tri-functional acrylamides), can be two of the factors at play.
Two-step total etch adhesives comprising UDMA (60 wt%) and 40 wt% of: TAAEA, TMAAEA (secondary, tertiary tri-acrylamides), BAAP, DEBAAP (secondary, tertiary di-acrylamides) or HEMA (mono-methacrylate - control) were formulated. Simulated composite restorations (n = 5) were tested after cyclic mechanical and biological (S. mutans biofilm) challenges. Gap formation before and after aging was assessed with SEM imaging. Micro-tensile bond strength (μTBS, n = 6) was assessed after seven-day incubation in water or S. mutans-containing culture medium. Collagen reinforcement was assessed with hydroxyproline assay (n = 10) and rheology (n = 3). Data were analyzed with one-way/two-way ANOVA/Tukey's test (alpha=5%).
Gap formation increased and bond strength decreased for all monomers after biofilm incubation (p < 0.001). Except for DEBAAP, secondary and tertiary di/tri-acrylamides showed lower occlusal gap width values, but no significant differences overall gap length compared to HEMA. μTBS increased for tri-acrylamides compared with HEMA. Samples treated with multi-acrylamides had lower concentration of hydroxyproline (by-product of collagen degradation) (p < 0.001), except for DEBAAP, which showed values close to HEMA (p > 0.05). Dentin shear modulus increased for all acrylamides after 72 h, especially TMAAEA.
In general, multi-acrylamides promote collagen reinforcement, leading to reduced gap formation, and stabilize the bond strength under physiological conditions.
丙烯酰胺显著提高了黏结修复体的稳定性,但增强机制尚未完全阐明。本研究假设,胶原网络的氢键增强(用二级或三级丙烯酰胺)以及聚合物网络的交联程度(用二或三官能丙烯酰胺)可能是两个起作用的因素之一。
采用两步全酸蚀黏结剂,包含 UDMA(60wt%)和 40wt%的:TAAEA、TMAAEA(二级、三级三丙烯酰胺)、BAAP、DEBAAP(二级、三级二丙烯酰胺)或 HEMA(单甲基丙烯酸酯-对照)。模拟复合修复体(n=5)在循环机械和生物(变形链球菌生物膜)挑战后进行测试。老化前后的间隙形成采用 SEM 成像评估。在水或含变形链球菌的培养基中孵育 7 天后,采用微拉伸黏结强度(μTBS,n=6)评估。采用羟脯氨酸测定法(n=10)和流变学(n=3)评估胶原增强。数据采用单向/双向 ANOVA/Tukey 检验(alpha=5%)进行分析。
生物膜孵育后,所有单体的间隙形成增加,黏结强度降低(p<0.001)。除 DEBAAP 外,二级和三级二/三丙烯酰胺的闭合间隙宽度值较低,但与 HEMA 相比,整体间隙长度无显著差异。与 HEMA 相比,三丙烯酰胺的 μTBS 增加。与 HEMA 相比,用多丙烯酰胺处理的样本羟脯氨酸浓度较低(胶原降解的副产物)(p<0.001),但 DEBAAP 除外,其值接近 HEMA(p>0.05)。72h 后,所有丙烯酰胺的牙本质剪切模量均增加,尤其是 TMAAEA。
一般来说,多丙烯酰胺可促进胶原增强,减少间隙形成,并在生理条件下稳定黏结强度。