Billington R W, Williams J A, Pearson G J
Biomaterials in Relation to Dentistry, Institute of Dentistry, Queen Mary University of London, Medical Science Building, Mile End Road, London E1 4NS, UK.
J Dent. 2006 Sep;34(8):544-55. doi: 10.1016/j.jdent.2005.09.008. Epub 2006 Mar 29.
Ion processes are involved in many aspects of glass-ionomer cements. The ions released from the glass take part in the formation of the cement matrix. Although this process has been investigated, particularly using model cement systems, no study provides a complete matrix composition. Combining results from different studies enables an approximate composition to be derived. The importance of Phosphorous in controlling ion release from the glass surface has been identified in a number of studies. The release of ions from the set cement into water (and other aqueous liquids) has been much reported, particularly for fluoride. Over most of the release periods studied (i.e. from >7 days up to 3 years), release of F ion is related to t1/2 indicating a diffusion-controlled process. Other ions, except possibly Na+ also show this relationship. The amount of cumulative F release whilst maintaining this relationship indicates that more F than is in the matrix is involved. Ion chromatography would probably elucidate the precise form of the ionic species released. Glass-ionomer cements take up ions from solutions in which they are immersed. The levels are much higher than required to produce as internal/external equilibrium. Studies using dynamic SIMS and XPS give some information on ion location and elemental association. It is suggested that ToF SIMS would elucidate these further. Re-release of uptaken ions can vary considerably for different cements and ion species. Surface disruption of glass ionomers is caused by both F ion and monofluorophosphate ion and occurs much more readily in F containing cements than in F free ones. The mechanism of this process has not been elucidated. Analysis of the ions released from the cement as disruption occurs should provide an indication of the site of attack.
离子过程涉及玻璃离子水门汀的许多方面。玻璃释放出的离子参与水门汀基质的形成。尽管这一过程已得到研究,尤其是使用模型水门汀体系,但尚无研究提供完整的基质组成。综合不同研究的结果能够得出近似的组成。许多研究已证实磷在控制玻璃表面离子释放方面的重要性。已大量报道了固化水门汀中的离子释放到水(及其他水性液体)中的情况,尤其是氟化物。在所研究的大部分释放期内(即从超过7天到3年),氟离子的释放与半衰期相关,表明这是一个扩散控制过程。除了可能的钠离子外,其他离子也呈现这种关系。在保持这种关系的同时,氟的累积释放量表明参与的氟比基质中的氟更多。离子色谱法可能会阐明释放出的离子物种的精确形式。玻璃离子水门汀会从其浸泡的溶液中吸收离子。吸收的离子水平远高于产生内部/外部平衡所需的水平。使用动态二次离子质谱和X射线光电子能谱的研究提供了一些关于离子位置和元素缔合的信息。有人认为飞行时间二次离子质谱将进一步阐明这些信息。对于不同的水门汀和离子物种,吸收离子的再释放情况可能有很大差异。玻璃离子水门汀的表面破坏是由氟离子和单氟磷酸根离子共同引起的,并且在含氟水门汀中比在无氟水门汀中更容易发生。这一过程的机制尚未阐明。分析破坏发生时从水门汀中释放出的离子应能指示攻击部位。