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Investigation of five α-hydroxy acids for enamel and dentin etching: Demineralization depth, resin adhesion and dentin enzymatic activity

机译:对牙釉质和牙本质蚀刻五α-羟基酸的研究:脱矿质深度,树脂粘附和牙本质酶活性

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Objectives. Surface conditioning of enamel and dentin is a key step during adhesive restorative procedures and strategies. The aim of this study was to investigate the effectiveness of five alpha-hydroxy-acids (AHAs) as enamel and dentin surface etchants.Methods. Enamel and dentin specimens were prepared from human molars to determine the depth of demineralization by optical profilometry (Delta z), the resin bond strength to enamel and dentin (mu TBS), the micro-permeability of dentin-resin interfaces, and the gelatinolytic activity of dentin matrix induced by AHAs [glycolic (GA), lactic (LA), citric (CA), malic (MI) and tartaric (TA)] and controls [phosphoric (PA) and maleic (MA)]. All acids were prepared at 35% concentration. Adhesion studies employed Adper Single Bond Plus bonding system. Data were individually processed and analyzed by ANOVA, post-hoc tests and Pearson correlations (alpha = 0.05).Results. AHA exhibited statistically lower depth of demineralization of enamel and dentin (average 4 fold) than controls (p 0.001). In enamel, MA and PA etching resulted in higher mu TBS than AHA groups (p 0.001). In dentin, GA, TA, CI and LA etching resulted in statistically similar mu TBS than PA (p 0.05). The hybrid-layer (HL) thickness and interfacial micro-permeability intensity were statistically lower for AHA groups (p 0.05). A significant positive correlation was observed between the intensity of micro-permeability and the thickness of HL (p 0.05). AHA etchants elicited lower dentin enzymatic activity than controls (p 0.05).Significance. AHAs effectively etched enamel and dentin surfaces. In particular, GA and TA resulted in suitable mu TBS and sealing ability as well as induced less gelatinolytic activity in dentin than PA and MA. (C) 2019 The Academy of Dental Materials. Published by Elsevier Inc. All rights reserved.
机译:目标。牙釉质和牙本质的表面调理是粘合恢复程序和策略期间的关键步骤。本研究的目的是探讨五种α-羟基酸(Ahas)作为牙釉质和牙本质表面蚀刻剂的有效性。方法。由人臼齿制备牙釉质和牙本质标本,以通过光学轮廓测定法(DELTA Z)确定脱矿质的深度,树脂粘合强度与牙釉质和牙本质(MU TBS),牙本质 - 树脂界面的微渗透性和凝胶溶解活性作者:王莹,王莹,王莹,王莹,王莹,王莹,王莹,王莹,王莹,王莹,王莹,王莹,王玮,王玮,王玮,王玮,王玮,王玮,王玮,王玮所有酸都以35%浓度制备。粘合性研究采用Adper单键加键合系统。通过ANOVA,HOC测试和PEARSON相关性分别处理和分析数据(Alpha = 0.05).Results。 AHA在牙植物和牙本质(平均4倍)的统计上较低的脱矿质深度而不是对照(P <0.001)。在牙釉质中,MA和PA蚀刻导致更高的MU TBS而不是AHA组(P <0.001)。在牙本质,Ga,Ta,Ci和La蚀刻中导致统计学上类似的mu tbs(p <0.05)。杂交层(HL)厚度和界面微渗透强度对于AHA基团具有统计学较低(P <0.05)。在微渗透性和HL厚度之间观察到显着的正相关性(P <0.05)。 AHA蚀刻剂引发了低于对照的牙本质酶活性(P <0.05)。重要性。 AHA有效地蚀刻牙釉质和牙本质表面。特别地,Ga和Ta导致Mu Tbs和密封能力以及牙本质中诱导的牙肽少于Pa和Ma。 (c)2019年牙科材料学院。由elsevier Inc.出版的所有权利保留。

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