Pawluk K, Booth S E, Coleman N J, Nicholson J W
Department of Environmental, Chemical and Pharmaceutical Sciences, School of Science, University of Greenwich, Medway Campus, Chatham, Kent ME4 4TB, UK.
J Mater Sci Mater Med. 2008 Sep;19(9):3035-9. doi: 10.1007/s10856-008-3443-0. Epub 2008 Apr 4.
The ability of zinc oxide-based dental cements (zinc phosphate and zinc polycarboxylate) to take up fluoride from aqueous solution has been studied. Only zinc phosphate cement was found to take up any measurable fluoride after 5 h exposure to the solutions. The zinc oxide filler of the zinc phosphate also failed to take up fluoride from solution. The key interaction for this uptake was thus shown to involve the phosphate groups of the set cement. However, whether this took the form of phosphate/fluoride exchange, or the formation of oxyfluoro-phosphate groups was not clear. Fluoride uptake followed radicaltime kinetics for about 2 h in some cases, but was generally better modelled by the Elovich equation, dq(t)/dt = alpha exp(-betaq(t)). Values for alpha varied from 3.80 to 2.48 x 10(4), and for beta from 7.19 x 10(-3) to 0.1946, though only beta showed any sort of trend, becoming smaller with increasing fluoride concentration. Fluoride was released from the zinc phosphate cements in processes that were diffusion based up to M(t)/M(infinity) of about 0.4. No further release occurred when specimens were placed in fresh volumes of deionised water. Only a fraction of the fluoride taken up was re-released, demonstrating that most of the fluoride taken up becomes irreversibly bound within the cement.
人们已经研究了氧化锌基牙科水门汀(磷酸锌和聚羧酸锌)从水溶液中吸收氟化物的能力。在将样品暴露于溶液5小时后,仅发现磷酸锌水门汀吸收了可测量的氟化物。磷酸锌的氧化锌填料也未能从溶液中吸收氟化物。因此,这种吸收的关键相互作用被证明涉及凝固水门汀的磷酸基团。然而,这是以磷酸/氟化物交换的形式发生,还是形成了氧氟磷酸基团尚不清楚。在某些情况下,氟化物吸收在约2小时内遵循自由基时间动力学,但通常用埃洛维奇方程dq(t)/dt =αexp(-βq(t))能更好地模拟。α值从3.80到2.48×10⁴不等,β值从7.19×10⁻³到0.1946不等,不过只有β呈现出某种趋势,随着氟化物浓度的增加而变小。氟化物从磷酸锌水门汀中释放的过程基于扩散,直到M(t)/M(∞)约为0.4。当将样品置于新鲜的去离子水中时,没有进一步的释放发生。吸收的氟化物中只有一小部分被重新释放,这表明吸收的大部分氟化物在水门汀内不可逆地结合。