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本文引用的文献

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Cure mechanisms in materials for use in esthetic dentistry.用于口腔美学修复材料的固化机制。
J Investig Clin Dent. 2012 Feb;3(1):3-16. doi: 10.1111/j.2041-1626.2012.00114.x.
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The effect of hydroxyapatite presence on the degree of conversion and polymerization rate in a model self-etching adhesive.羟磷灰石的存在对模型自酸蚀黏合剂的转化率和聚合速率的影响。
Dent Mater. 2012 Mar;28(3):237-44. doi: 10.1016/j.dental.2011.10.003. Epub 2011 Oct 26.
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Improved degree of conversion of model self-etching adhesives through their interaction with dentine.通过与牙本质的相互作用提高模型自酸蚀黏合剂的转化率。
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Comparing the effectiveness of self-curing and light curing in polymerization of dual-cured core buildup materials.比较自凝和光固化在双重固化核堆积材料聚合中的效果。
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State of the art etch-and-rinse adhesives.先进的酸蚀-冲洗型粘结剂。
Dent Mater. 2011 Jan;27(1):1-16. doi: 10.1016/j.dental.2010.10.016. Epub 2010 Nov 27.
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State of the art of self-etch adhesives.自酸蚀粘接剂的现状。
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A review of the development of radical photopolymerization initiators used for designing light-curing dental adhesives and resin composites.自由基光引发剂用于设计光固化牙科胶粘剂和树脂复合材料的发展综述。
Dent Mater J. 2010 Oct;29(5):481-501. doi: 10.4012/dmj.2009-137. Epub 2010 Sep 16.
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Degree of conversion and interfacial nanoleakage expression of three one-step self-etch adhesives.三种一步法自酸蚀粘结剂的固化程度及界面纳米渗漏表现
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The use of nanoindentation for characterizing the properties of mineralized hard tissues: state-of-the art review.利用纳米压痕技术表征矿化硬组织的特性:最新综述
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Systematic review of the chemical composition of contemporary dental adhesives.当代牙科粘合剂化学成分的系统评价。
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羟基磷灰石诱导模型自酸蚀牙科胶粘剂的自发聚合。

Hydroxyapatite induces spontaneous polymerization of model self-etch dental adhesives.

机构信息

Center for Research on Interfacial Structure and Properties, University of Missouri-Kansas City, Kansas City, MO 64108, USA.

出版信息

Mater Sci Eng C Mater Biol Appl. 2013 Oct;33(7):3670-6. doi: 10.1016/j.msec.2013.04.053. Epub 2013 May 3.

DOI:10.1016/j.msec.2013.04.053
PMID:23910263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3760264/
Abstract

The objective of this study is to report for the first time the spontaneous polymerization phenomenon of self-etch dental adhesives induced by hydroxylapatite (HAp). Model self-etch adhesives were prepared by using a monomer mixture of bis[2-(methacryloyloxy)ethyl] phosphate (2MP) with 2-hydroxyethyl methacrylate (HEMA). The initiator system consisted of camphorquinone (CQ, 0.022 mmol/g) and ethyl 4-dimethylaminobenzoate (4E, 0.022-0.088 mmol/g). HAp (2-8 wt.%) was added to the neat model adhesive. In a dark environment, the polymerization was monitored in-situ using ATR/FT-IR, and the mechanical properties of the polymerized adhesives were evaluated using nanoindentation technique. Results indicated that spontaneous polymerization was not observed in the absence of HAp. However, as different amounts of HAp were incorporated into the adhesives, spontaneous polymerization was induced. Higher HAp content led to higher degree of conversion (DC), higher rate of polymerization (RP) and shorter induction period (IP). In addition, higher 4E content also elevated DC and RP and reduced IP of the adhesives. Nanoindentation result suggested that the Young's modulus of the polymerized adhesives showed similar dependence on HAp and 4E contents. In summary, interaction with HAp could induce spontaneous polymerization of the model self-etch adhesives. This result provides important information for understanding the initiation mechanism of the self-etch adhesives, and may be of clinical significance to strengthen the adhesive/dentin interface based on the finding.

摘要

本研究的目的是首次报道羟基磷灰石(HAp)诱导自酸蚀牙本质粘结剂的自发聚合现象。模型自酸蚀粘结剂通过使用双[2-(甲基丙烯酰氧基)乙基]磷酸酯(2MP)与 2-羟乙基甲基丙烯酸酯(HEMA)的单体混合物来制备。引发剂体系由樟脑醌(CQ,0.022mmol/g)和乙基 4-二甲氨基苯甲酸酯(4E,0.022-0.088mmol/g)组成。将 HAp(2-8wt.%)添加到纯模型粘结剂中。在黑暗环境中,使用 ATR/FT-IR 原位监测聚合反应,并使用纳米压痕技术评估聚合粘结剂的机械性能。结果表明,在没有 HAp 的情况下未观察到自发聚合。然而,随着 HAp 量的不同,自发聚合被诱导。较高的 HAp 含量导致更高的转化率(DC)、更高的聚合速率(RP)和更短的诱导期(IP)。此外,较高的 4E 含量也提高了粘结剂的 DC 和 RP,并降低了 IP。纳米压痕结果表明,聚合粘结剂的杨氏模量表现出对 HAp 和 4E 含量的相似依赖性。总之,与 HAp 的相互作用可以诱导模型自酸蚀粘结剂的自发聚合。这一结果为理解自酸蚀粘结剂的引发机制提供了重要信息,并且基于这一发现,可能对增强粘结剂/牙本质界面具有临床意义。