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Comparative evaluation of fluoride varnishes, self-assembling peptide-based remineralization agent, and enamel matrix protein derivative on artificial enamel remineralization in vitro

机译:氟化物清漆,自组装肽的再矿化剂和牙釉质基质蛋白衍生物对人工搪瓷再矿化的比较评价

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Background One of the most unfavorable side effects of fixed orthodontic treatment is white spot lesions (WSLs). Although the most important approach is prevention of WSLs, it is also essential to evaluate the efficacy of the remineralization agents. However, there is no concurrence in the literature with respect to the remineralization process of these agents. The objective of the present study was to evaluate the effects of different fluoride varnishes, enamel matrix protein, and self-assembling peptide derivatives with varying chemical compositions on remineralization of artificially created WSLs in vitro using quantitative light-induced fluorescence (QLF). Methods Artificial WSLs were created on bovine enamel samples using acidic buffer solution (pH?5, 10?days). Specimens were randomly allocated to six groups ( n = 10/group): (1) Emdogain (Straumann, Basel, Switzerland), (2) Curodont Repair (Credentis AG, Switzerland), (3) Duraphat (Colgate-Palmolive, New York, NY), (4) Clinpro XT (3?M ESPE, Pymble, New South Wales, Australia), (5) Enamel Pro Varnish (Premier Dental Products, PA, USA), and (6) control (untreated). The agents were applied to the WSLs according to the manufacturers’ instructions. Fluorescence loss (Δ F ), lesion area (area), and impact (Δ Q ) values of enamel surfaces were quantified by QLF-D Biluminator ~(TM) (Inspektor-Pro, Amsterdam, The Netherlands) at baseline and after 7, 14, and 21?days of application of the respective materials. Results Δ F value presented a significantly decreasing trend throughout the 21?days for all groups except the Duraphat and Enamel Pro varnishes. The changes between 14th and 21st days of the Clinpro XT varnish application were significantly higher than Emdogain, Curodont, and Enamel Pro. The Curodont group showed higher lesion area changes between the first and second week in comparison to the Emdogain, Clinpro XT, and Enamel Pro groups, whereas Clinpro XT assured the highest reduction from the second to the third week of the observation period. Conclusions The fluorescence loss was significantly reduced with enamel matrix protein, self-assembling peptide, and light-curable fluoride varnishes in the analysis for 21?days. Curodont and Clinpro XT were effective in diminishing the fluorescence loss and lesion area compared to the Duraphat, Enamel Pro fluoride varnishes, and Emdogain in different time points.
机译:背景技术固定正畸治疗的最不利副作用之一是白斑病变(WSL)。虽然最重要的方法是预防WSL的方法,但也必须评估再矿化剂的功效。然而,关于这些药剂的再矿化过程,文献中没有任何同意。本研究的目的是评估不同氟化物清漆,牙釉质基质蛋白和自组装肽衍生物,其使用定量光诱导的荧光(QLF)在体外在体外进行改变的化学组合物对实体产生的WSL的再矿化。方法使用酸性缓冲溶液(pHα5,10≤天)在牛釉质样品上产生人造WSL。将标本随机分配给六组(n = 10 /组):(1)Emdogain(Straumann,Basel,瑞士),(2)Curodont修复(瑞士信NentisAG),(3)Duraphat(Colgate-Palmolive,纽约,NY),(4)Clinpro XT(3?MESPE,Pymble,New South Wales,Australia),(5)enamel Pro清漆(Premier Dental Products,Pa,USA)和(6)控制(未经处理)。根据制造商的指示将药剂应用于WSL。荧光损失(δf),病变区域(面积)和牙釉质表面的影响(δq)通过基线和7后的QLF-D双子杆菌(TM)(Inspektor-pro,Amsterdam,荷兰)量化牙釉质表面的量化14和21?施加各个材料的天数。结果ΔF值在除了DURAphat和Enamel Pro清漆之外的所有组的整个组的趋势显着降低。 ClinPro XT清漆应用的第14和21天的变化显着高于Emdogain,Curodont和Enamel Pro。 Curodont组在与Emdogain,ClinPro XT和搪瓷Pro组相比,第一周和第二周之间的病变区变化更高,而ClinPro XT则确保从观察期的第二个至第三周的最高减少。结论分析中的牙釉质基质蛋白,自组装肽和可光固化氟化物清漆显着降低了荧光损失。与DURAphat,搪瓷促氟化物清漆和不同时间点的Emdogain相比,Curodont和ClinPro XT有效减少荧光损失和病变区域。

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