Department of Morphology, Dental School of Piracicaba, University of Campinas, Piracicaba, Avenida Limeira, 901, 13414-903 Piracicaba, SP, Brazil.
Spectrochim Acta A Mol Biomol Spectrosc. 2010 Sep 15;77(1):59-63. doi: 10.1016/j.saa.2010.04.024. Epub 2010 May 5.
Details on how fluoride interferes in enamel mineralization are still controversial. Therefore, this study aimed at analyzing the organic contents of fluorosis-affected teeth using Fourier Transformation Infrared spectroscopy. To this end, 10 male Wistar rats were divided into two groups: one received 45 ppm fluoride in distilled water for 60 days; the other received distilled water only. Then, the lower incisors were removed and prepared for analysis by two FTIR techniques namely, transmission and micro-ATR. For the first technique, the enamel was powdered, whereas in the second case one fluorotic incisor was cut longitudinally for micro-ATR. Using transmission and powdered samples, FTIR showed a higher C-H content in the fluorotic enamel compared with control enamel (p<0.05, n=4 in the flurotic, and n=5 in the control group). Results from the micro-ATR-FTIR spectroscopic analysis on one longitudinally cut incisor carried out at six points reveal a higher C-H bond content at the surface of the enamel, with values decreasing toward the dentine-enamel junction, and reaching the lowest values at the subsuperficial enamel. These results agree with the morphological data, which indicate that in the rat incisor the fluorotic lesion is superficial, rather than subsuperficial, as in the case of human enamel. The results also suggest that the increased C-H bond content may extend toward the more basal enamel (intraosseous), indicating that fluorotic enamel may intrinsically contain more protein. Finally, particularly when coupled to ATR, FTIR is a suitable tool to study the rat incisor enamel, which is a largely used model of normal and abnormal amelogenesis. Further studies along this line may definitely answer some questions regarding protein content in fluorotic enamel as well as their origin.
氟化物如何干扰釉质矿化的细节仍存在争议。因此,本研究旨在使用傅里叶变换红外光谱分析氟斑牙的有机含量。为此,将 10 只雄性 Wistar 大鼠分为两组:一组用蒸馏水给予 45ppm 的氟,共 60 天;另一组仅用蒸馏水。然后,取下下切牙并通过两种 FTIR 技术(透射和微 ATR)进行分析。对于第一种技术,釉质被粉碎,而在第二种情况下,一个氟斑牙被纵向切割用于微 ATR。使用透射和粉末样本,FTIR 显示氟斑釉质中的 C-H 含量高于对照组(p<0.05,氟斑组 n=4,对照组 n=5)。在六个点上对一个纵向切割的切牙进行的微 ATR-FTIR 光谱分析的结果显示,釉质表面的 C-H 键含量较高,值从釉牙骨质界向牙本质方向降低,并在釉下浅层达到最低值。这些结果与形态学数据一致,表明在大鼠切牙中,氟斑病变是浅表的,而不是人类釉质的亚表层。结果还表明,增加的 C-H 键含量可能延伸到更基底的釉质(骨内),表明氟斑釉质可能内在含有更多的蛋白质。最后,特别是当与 ATR 结合时,FTIR 是研究大鼠切牙釉质的合适工具,大鼠切牙釉质是正常和异常釉质发生的常用模型。沿着这条线进行的进一步研究肯定会回答一些关于氟斑牙中蛋白质含量及其来源的问题。