Bioengineering Research Center, University of Kansas, Lawrence, Kansas 66045-7609, USA.
J Biomed Mater Res B Appl Biomater. 2012 May;100(4):1086-92. doi: 10.1002/jbm.b.32675. Epub 2012 Feb 14.
There have been reports of the sensitivity of our current dentin adhesives to excess moisture, for example, water-blisters in adhesives placed on over-wet surfaces, and phase separation with concomitant limited infiltration of the critical dimethacrylate component into the demineralized dentin matrix. To determine quantitatively the hydrophobic/hydrophilic components in the aqueous phase when exposed to over-wet environments, model adhesives were mixed with 16, 33, and 50 wt % water to yield well-separated phases. Based upon high-performance liquid chromatography coupled with photodiode array detection, it was found that the amounts of hydrophobic BisGMA and hydrophobic initiators are less than 0.1 wt % in the aqueous phase. The amount of these compounds decreased with an increase in the initial water content. The major components of the aqueous phase were hydroxyethyl methacrylate (HEMA) and water, and the HEMA content ranged from 18.3 to 14.7 wt %. Different BisGMA homologues and the relative content of these homologues in the aqueous phase have been identified; however, the amount of crosslinkable BisGMA was minimal and, thus, could not help in the formation of a crosslinked polymer network in the aqueous phase. Without the protection afforded by a strong crosslinked network, the poorly photoreactive compounds of this aqueous phase could be leached easily. These results suggest that adhesive formulations should be designed to include hydrophilic multimethacrylate monomers and water compatible initiators.
已有报道称,我们目前的牙本质黏合剂对过量水分敏感,例如,放置在过湿表面上的黏合剂会出现水疱,以及相分离,同时伴随着二甲基丙烯酸酯成分有限地渗透到脱矿质牙本质基质中。为了定量确定在过湿环境下暴露时水相中的疏水性/亲水性成分,将模型黏合剂与 16、33 和 50wt%的水混合,以产生良好分离的相。通过高效液相色谱法与光电二极管阵列检测相结合,发现水相中的疏水性 BisGMA 和疏水性引发剂的含量均小于 0.1wt%。这些化合物的含量随着初始含水量的增加而减少。水相的主要成分是羟乙基甲基丙烯酸酯(HEMA)和水,HEMA 含量范围为 18.3%至 14.7%。已鉴定出不同的 BisGMA 同系物及其在水相中的相对含量;然而,可交联 BisGMA 的量很小,因此无法帮助在水相中原位形成交联聚合物网络。如果没有强交联网络提供的保护,水相中这些光反应性差的化合物很容易被浸出。这些结果表明,黏合剂配方应设计为包含亲水性多甲基丙烯酸酯单体和水相容的引发剂。