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受不同碳链单体影响的黏附界面相互作用。

Adhesive interfacial interaction affected by different carbon-chain monomers.

机构信息

KU Leuven BIOMAT, Department of Oral Health Research, KU Leuven (University of Leuven) & Dentistry, University Hospitals Leuven, Belgium.

出版信息

Dent Mater. 2013 Aug;29(8):888-97. doi: 10.1016/j.dental.2013.05.006. Epub 2013 Jun 13.

Abstract

OBJECTIVES

The functional monomer 10-methacryloxydecyl dihydrogen phosphate (10-MDP), recently used in more self-etch adhesives, chemically bonds to hydroxyapatite (HAp) and thus tooth tissue. Although the interfacial interaction of the phosphoric-acid functional group of 10-MDP with HAp-based substrates has well been documented, the effect of the long carbon-chain spacer of 10-MDP on the bonding effectiveness is far from understood.

METHODS

We investigated three phosphoric-acid monomers, 2-methacryloyloxyethyl dihydrogen phosphate (2-MEP), 6-methacryloyloxyhexyl dihydrogen phosphate (6-MHP) and 10-MDP, that only differed for the length of the carbon chain, on their chemical interaction potential with HAp and dentin, this correlatively using X-ray diffraction (XRD) and transmission electron microscopy (TEM). Commercial 6-MHP and 10-MDP containing adhesives were investigated as well.

RESULTS

XRD revealed that on HAp only 10-MDP produced monomer-calcium salts in the form of 'nano-layering', while on dentin all monomers produced 'nano-layering', but with a varying intensity in the order of 10-MDP>6-MHP>2-MEP. TEM confirmed that 10-MDP formed the thickest hybrid and adhesive layer. XRD and TEM revealed 'nano-layering' for all commercial adhesives on dentin, though less intensively for the 6-MHP containing adhesive than for the 10-MDP ones.

SIGNIFICANCE

It is concluded that not only the phosphoric-acid group but also the spacer group, and its length, affect the chemical interaction potential with HAp and dentin. In addition, the relatively strong 'etching' effect of 10-MDP forms more stable monomer-Ca salts, or 'nano-layering', than the two shorter carbon-chain monomers tested, thereby explaining, at least in part, the better bond durability documented with 10-MDP containing adhesives.

摘要

目的

最近在更多自酸蚀粘结剂中使用的功能单体 10-甲氧基癸基二氢磷酸酯(10-MDP)通过化学键与羟基磷灰石(HAp)和牙本质结合。尽管 10-MDP 的磷酸基团与 HAp 基基底的界面相互作用已经得到很好的证明,但 10-MDP 的长碳链间隔基对粘结效果的影响还远未被理解。

方法

我们研究了三种磷酸单体,即 2-甲基丙烯酰氧基乙基二氢磷酸酯(2-MEP)、6-甲基丙烯酰氧基己基二氢磷酸酯(6-MHP)和 10-MDP,它们仅在碳链长度上有所不同,研究了它们与 HAp 和牙本质的化学相互作用潜力,这通过 X 射线衍射(XRD)和透射电子显微镜(TEM)进行了相关研究。同时还研究了商业的含有 6-MHP 和 10-MDP 的粘结剂。

结果

XRD 表明,在 HAp 上,只有 10-MDP 以“纳米层状”的形式产生单体-钙盐,而在牙本质上,所有单体都产生“纳米层状”,但强度顺序为 10-MDP>6-MHP>2-MEP。TEM 证实 10-MDP 形成了最厚的混合层和粘结层。XRD 和 TEM 表明,所有商业粘结剂在牙本质上都存在“纳米层状”,但含有 6-MHP 的粘结剂的强度不及含有 10-MDP 的粘结剂。

意义

研究结论认为,不仅是磷酸基团,而且是间隔基及其长度,都会影响与 HAp 和牙本质的化学相互作用潜力。此外,10-MDP 的相对较强的“蚀刻”效应形成了比测试的两种较短碳链单体更稳定的单体-Ca 盐,或“纳米层状”,这至少部分解释了含有 10-MDP 的粘结剂具有更好的粘结耐久性。

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