Gao W, Smales R J, Gale M S
Department of Prosthodontics, School of Stomatology, Beijing Medical University, PR China.
Am J Dent. 2000 Aug;13(4):201-4.
To determine the fluoride ion release/uptake of two conventional glass-ionomer cements (GICs) manufactured for use with the ART approach (Fuji IX GP, Ketac-Molar), as compared with that of a resin-modified GIC (Fuji II LC).
15 specimens of each material were prepared and placed in vials with artificial saliva and stored at 37 degrees C. The solution was replaced weekly for 6 wks, and the fluoride ions released were measured in ppm each week. After 6 wks, the 15 specimens of each material were divided into three equal groups and placed into three fluoride recharging agents (1.23% APF gel, 1.1% neutral NaF and 0.001% CaF2) for 4 min at 23 degrees C. Fluoride ion measurements of the recharged specimens were carried out at 1 day, 2 days, then weekly for another 6 wks.
All freshly-mixed specimens showed the highest fluoride ion release after 1 week, then the release rates dropped quickly to become largely stabilized after 3 wks. After one 4-min exposure to APF gel the initial fluoride ion release increased significantly for all materials. The highest rates were during the first day, but then dropped very quickly to again become largely stabilized after usually 3 wks. Exposure to NaF and CaF2 did not usually result in significantly sustained fluoride ion release by any material. The order of release/uptake for all three agents was Fuji II LC > Fuji IX GP > Ketac-Molar. The mechanism of fluoride ion release after the application of different fluoride recharging agents is not clear. It may occur partly by washout of recharge agents that are retained in the pores and cracks of the restorative materials, for APF gel is viscous and difficult to wash off completely with deionized water; by erosion of surfaces by low pH agents, or by the subsequent release of fluoride ions from within the cement matrix.
测定两种用于非创伤性修复治疗(ART)方法的传统玻璃离子水门汀(GIC)(富士IX GP、Ketac-Molar)与树脂改性玻璃离子水门汀(富士II LC)相比的氟离子释放/摄取情况。
每种材料制备15个样本,置于装有人工唾液的小瓶中,在37℃下储存。每周更换溶液,持续6周,每周测量释放的氟离子浓度(以ppm计)。6周后,将每种材料的15个样本平均分为三组,置于三种氟化物再充电剂(1.23%酸性磷酸氟凝胶、1.1%中性氟化钠和0.001%氟化钙)中,在23℃下放置4分钟。对再充电后的样本在第1天、第2天进行氟离子测量,然后再持续6周每周测量一次。
所有新混合的样本在1周后显示出最高的氟离子释放量,然后释放速率迅速下降,在3周后基本稳定。所有材料在暴露于酸性磷酸氟凝胶4分钟后,初始氟离子释放量显著增加。最高释放速率出现在第一天,但随后迅速下降,通常在3周后再次基本稳定。暴露于氟化钠和氟化钙通常不会导致任何材料的氟离子持续显著释放。三种试剂的释放/摄取顺序为富士II LC>富士IX GP>Ketac-Molar。应用不同氟化物再充电剂后氟离子释放的机制尚不清楚。可能部分是由于保留在修复材料孔隙和裂缝中的再充电剂被冲洗掉,因为酸性磷酸氟凝胶具有粘性,难以用去离子水完全冲洗掉;是由于低pH试剂对表面的侵蚀,或者是由于随后从水门汀基质中释放氟离子。