Dental Biomaterials, Biomaterials Department, Faculty of Dentistry, Ain-Shams University, Organization of African unity street, El-Qobba Bridge, El-Weili, Cairo, Egypt.
BMC Oral Health. 2024 Feb 27;24(1):279. doi: 10.1186/s12903-024-04008-z.
Several methods were introduced for enamel biomimetic remineralization that utilize a biomimetic analogue to interact and absorb bioavailable calcium and phosphate ions and induce crystal nucleation on demineralized enamel. Amelogenin is the most predominant enamel matrix protein that is involved in enamel biomineralization. It plays a major role in developing the enamel's hierarchical microstructure. Therefore, this study was conducted to evaluate the ability of an amelogenin-inspired peptide to promote the remineralization potential of fluoride and a supersaturated calcium phosphate solution in treating artificially induced enamel carious lesions under pH-cycling regimen.
Fifty enamel slices were prepared with a window (4*4 mm ) on the surface. Five samples were set as control healthy enamel and 45 samples were subjected to demineralization for 3 days. Another 5 samples were set as control demineralized enamel and 40 enamel samples were assigned into 8 experimental groups (n=5) (P/I, P/II, P/III, P/AS, NP/I, NP/II, NP/III and NP/AS) according to peptide treatment (peptide P or non-peptide NP) and remineralizing solution used (I; calcium phosphate solution, II; calcium phosphate fluoride solution, III; fluoride solution and AS; artificial saliva). Samples were then subjected to demineralization/remineralization cycles for 9 days. Samples in all experimental groups were evaluated using Raman spectroscopy for mineral content recovery percentage, microhardness and nanoindentation as healthy, demineralized enamel and after pH-cycling. Data were statistically analysed using two-way repeated measures Anova followed by Bonferroni-corrected post hoc test for pairwise multiple comparisons between groups. Statistical significance was set at p= 0.05. Additionally, XRD, FESEM and EDXS were used for crystal orientation, surface morphology and elemental analysis after pH-cycling.
Nanocrystals clumped in a directional manner were detected in peptide-treated groups. P/II showed the highest significant mean values in mineral content recovery (63.31%), microhardness (268.81±6.52 VHN), elastic modulus (88.74±2.71 GPa), nanohardness (3.08±0.59 GPa) and the best crystal orientation with I/ (1.87±0.08).
Despite pH changes, the tested peptide was capable of remineralizing enamel with ordered crystals. Moreover, the supplementary use of calcium phosphate fluoride solution with peptide granted an enhancement in enamel mechanical properties after remineralization.
有几种方法被引入用于牙釉质仿生再矿化,这些方法利用仿生类似物与生物可利用的钙和磷酸盐离子相互作用和吸收,并在脱矿牙釉质上诱导晶体成核。釉原蛋白是参与牙釉质生物矿化的最主要的釉质基质蛋白。它在形成牙釉质的分级微观结构中起着主要作用。因此,本研究旨在评估一种釉原蛋白模拟肽在 pH 循环方案下,用氟化物和过饱和磷酸钙溶液处理人工诱导的牙釉质龋损时,促进再矿化潜力的能力。
在表面制备 50 个带有窗口(4*4mm)的牙釉质切片。5 个样本作为健康牙釉质对照,45 个样本进行 3 天脱矿处理。另外 5 个样本作为对照脱矿牙釉质,40 个牙釉质样本根据肽处理(肽 P 或非肽 NP)和再矿化溶液(I;磷酸钙溶液,II;磷酸钙氟化物溶液,III;氟化物溶液和 AS;人工唾液)分为 8 个实验组(n=5)(P/I、P/II、P/III、P/AS、NP/I、NP/II、NP/III 和 NP/AS)。然后,样品进行 9 天的脱矿/再矿化循环。所有实验组的样本均使用拉曼光谱法评估矿化含量恢复百分比、显微硬度和纳米压痕,以评估健康、脱矿牙釉质和 pH 循环后的状态。使用双向重复测量方差分析(ANOVA)对数据进行统计学分析,然后使用 Bonferroni 校正后检验进行组间两两多重比较。统计学意义设定为 p=0.05。此外,XRD、FESEM 和 EDXS 用于 pH 循环后的晶体取向、表面形态和元素分析。
在肽处理组中检测到定向聚集的纳米晶体。P/II 显示出最高的矿化含量恢复(63.31%)、显微硬度(268.81±6.52 VHN)、弹性模量(88.74±2.71 GPa)、纳米硬度(3.08±0.59 GPa)和最佳晶体取向 I/(1.87±0.08)的显著平均值。
尽管 pH 值发生变化,测试的肽仍能够使牙釉质再矿化形成有序的晶体。此外,在再矿化过程中,用氟化物和磷酸钙溶液补充使用肽可提高牙釉质的机械性能。