Zhang Yue, Huang Rui-zhe
Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, Clinical Research Center of Shannxi Province for Dental and Maxillofacial Diseases, College of Stomatology, Xi'an Jiaotong University. Xi'an 710004,China. E-mail:
Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, Clinical Research Center of Shannxi Province for Dental and Maxillofacial Diseases, College of Stomatology, Xi'an Jiaotong University. Xi'an 710004,China.
Shanghai Kou Qiang Yi Xue. 2016 Feb;25(1):42-6.
The phase of new substances and the effect on enamel lattice was analysed after ferrous sulfate ,sodium fluoride treatment through X-ray diffraction, in order to explore the mechanism of Fe2+ and F- reinforced enamel acid resistance.
Fragments of enamel obtained from fifty molars were ground into powder and randomly divided into four groups: C (control,deionized water); Fe2+ (15 mmol/L FeSO4); F- (1.23% NaF) and Fe2++F- (15 mmol/L FeSO4 and 1.23% NaF). Before exposure to acid, the samples were incubated in one of the experimental solutions for 48 hours. After that, the samples were submitted to six alternating remineralization and demineralization cycles. A complete cycle consisted of the following steps:① demineralization in 5 mL of the beverage (Coca-Cola, pH=2.58) for 5 minutes under gentle agitation;② remineralization in 5 mL of artificial saliva for 1 hour at 37℃. X-ray diffraction was employed to identify precipitates and estimate their lattice constants before enamel power dried at 40℃.
The XRD pattern of the group of ferrous sulfate was not sharper than control while the full width half maximum of peak increased and became more gentle. The enamel crystal grain size and crystallinity decreased. Secondary phase retrieval showed there was new phase formed which was iron phosphate. Diffraction spectrum of ferrous sulfate with fluoride group was similar to fluoride alone, the full width half maximum of peak became sharper and more narrow.The enamel crystal grain crystallinity improved and there was new phase of calcium fluoride formed.
Fe2+ and F- both had certain influence on the crystal structure of enamel. However, the impact of Fe2+ was concealed when reacted with high concentration F-. Fe2+ may participate in the nucleation of apatite through substitution of calcium in apatite. Acid-resistant enamel surfaces are established due to precipitation of ferric phosphates on the enamel surface, and combination of Fe2+ with PO4(3-) dissolved on enamel surface. F- may participate in the nucleation of apatite through substitution of OH-; at the same time, the calcium fluoride precipitation was established.
通过X射线衍射分析硫酸亚铁、氟化钠处理后新物质的物相及对牙釉质晶格的影响,以探讨Fe²⁺与F⁻增强牙釉质抗酸性的机制。
将从50颗磨牙获取的牙釉质碎片研磨成粉末,随机分为四组:C组(对照组,去离子水);Fe²⁺组(15 mmol/L硫酸亚铁);F⁻组(1.23%氟化钠);Fe²⁺+F⁻组(15 mmol/L硫酸亚铁和1.23%氟化钠)。在酸处理前,将样本在其中一种实验溶液中孵育48小时。之后,对样本进行六个交替的再矿化和脱矿化循环。一个完整的循环包括以下步骤:①在5 mL饮料(可口可乐,pH = 2.58)中轻轻搅拌下脱矿化5分钟;②在5 mL人工唾液中于37℃再矿化1小时。在40℃干燥牙釉质粉末前,采用X射线衍射鉴定沉淀物并估计其晶格常数。
硫酸亚铁组的X射线衍射图谱不如对照组清晰,峰的半高宽增加且变得更平缓。牙釉质晶粒尺寸和结晶度降低。次生相检索显示有新相形成,即磷酸铁。硫酸亚铁与氟化物组的衍射光谱与单独氟化物相似,峰的半高宽变得更尖锐、更窄。牙釉质晶粒结晶度提高,并有氟化钙新相形成。
Fe²⁺和F⁻均对牙釉质晶体结构有一定影响。然而,当与高浓度F⁻反应时,Fe²⁺的影响被掩盖。Fe²⁺可能通过取代磷灰石中的钙参与磷灰石的成核。由于磷酸铁在牙釉质表面沉淀以及Fe²⁺与牙釉质表面溶解的PO₄³⁻结合,形成了抗酸牙釉质表面。F⁻可能通过取代OH⁻参与磷灰石的成核;同时,形成了氟化钙沉淀。