Lopes Guilherme Carpena, Spohr Ana Maria, De Souza Grace M
J Adhes Dent. 2016;18(3):239-46. doi: 10.3290/j.jad.a36137.
To evaluate the effect of different bonding strategies on short- and long-term bis-GMA-based resin cement bond strengths to zirconia.
One hundred twenty samples of fully-sintered zirconia (Prettau Zirconia) were sandblasted and randomly distributed into 5 groups (n = 24): UA: Scotchbond Universal Adhesive; SZP: Signum Zirconia Bond I + II; ZPP: Z-Prime Plus; EXP: MZ experimental primer; CO: no primer application (control). After performing these surface treatments, translucent tubes (0.8 mm diameter and 1.0 mm height) were placed on the zirconia specimens, and bis-GMA-based cement (Duo-Link) was injected into them and light cured. Specimens were tested for microshear bond strength either 24 h or 6 months (m) after water storage (37°C) and surfaces were characterized by SEM and EDX. Two-way ANOVA and Tukey's post-hoc test (p < 0.05) were used to evaluate bond strength results.
The mean bond strengths (MPa ± SD) were: UA=14.6 ± 4.7a (24 h); 16.0 ± 4.8a (6 m); SZP = 14.0 ± 5.4ab (24 h); 11.9 ± 2.6ab (6 m); ZPP=8.0 ± 1.8b (24 h); 8.6 ± 3.3b (6 m); EXP = 1.2 ± 0.5c (24 h); 0.6 ± 0.7c (6 m); CO=1.0 ± 1.2c (24 h); 1.3 ± 1.2c (6 m). Bonding strategy significantly influenced bond strength (p = 0.0001), but storage time did not (p = 0.841). Groups UA and SZP showed a homogeneous layer covering the zirconia surface. In these groups, EDX demonstrated the presence of phosphorus. Group ZPP resulted in a nonhomogeneous layer, exposing the zirconia substrate underneath. EXP application resulted in an undetectable layer.
Water storage did not affect resin cement bond strengths to zirconia irrespective of the surface treatment. Bis-GMA-based resin cement bond strengths to zirconia are affected by specific bonding strategies.
评估不同粘结策略对基于双甲基丙烯酸缩水甘油酯(bis-GMA)的树脂水门汀与氧化锆短期和长期粘结强度的影响。
将120个完全烧结的氧化锆样本(Prettau氧化锆)进行喷砂处理,并随机分为5组(n = 24):UA组:Scotchbond通用粘结剂;SZP组:Signum氧化锆粘结剂I + II;ZPP组:Z-Prime Plus;EXP组:MZ实验性底漆;CO组:不使用底漆(对照组)。进行这些表面处理后,将半透明管(直径0.8 mm,高1.0 mm)放置在氧化锆试件上,并注入基于bis-GMA的水门汀(Duo-Link),然后光固化。试件在37°C水储存24小时或6个月后测试其微剪切粘结强度,并用扫描电子显微镜(SEM)和能谱仪(EDX)对表面进行表征。采用双向方差分析和Tukey事后检验(p < 0.05)评估粘结强度结果。
平均粘结强度(MPa ±标准差)为:UA组:24小时为14.6 ± 4.7a;6个月为16.0 ± 4.8a;SZP组:24小时为14.0 ± 5.4ab;6个月为11.9 ± 2.6ab;ZPP组:24小时为8.0 ± 1.8b;6个月为8.6 ± 3.3b;EXP组:24小时为1.2 ± 0.5c;6个月为0.6 ± 0.7c;CO组:24小时为1.0 ± 1.2c;6个月为1.3 ± 1.2c。粘结策略对粘结强度有显著影响(p = 0.0001),但储存时间没有影响(p = 0.841)。UA组和SZP组显示有一层均匀的覆盖层覆盖氧化锆表面。在这些组中,EDX显示存在磷。ZPP组形成不均匀层,暴露了下面的氧化锆基底。使用EXP底漆后形成不可检测的层。
无论表面处理如何,水储存均不影响树脂水门汀与氧化锆的粘结强度。基于bis-GMA的树脂水门汀与氧化锆的粘结强度受特定粘结策略的影响。