Department of Maxillary Orthopaedics, Medical University of Lublin, 20-093 Lublin, Poland.
Department of Orthopaedics and Rehabilitation, Medical University of Lublin, 20-059 Lublin, Poland.
Int J Mol Sci. 2024 Oct 21;25(20):11297. doi: 10.3390/ijms252011297.
This study primarily focused on the acid erosion of enamel and dentin. A detailed examination of the X-ray diffraction data proves that the products of the acid-caused decay of enamel belong to the family of isomorphic bioapatites, especially calcium-deficient hydroxyapatites. They are on a trajectory towards less and less crystallized substances. The increase in Bragg's parameter d and the decrease in the energy necessary for the changes were coupled with variability in the pH. This was valid for the corrosive action of acid solutions with a pH greater than 3.5. When the processes of natural tooth aging were studied by X-ray diffraction, a clear similarity to the processes of the erosion of teeth was revealed. Scarce data on osteoporotic bones seemed to confirm the conclusions derived for teeth. The data concerning the bioapatite decays were confronted with the cycles of apatite synthesis/decay. The chemical studies, mainly concerning the Ca/P ratio in relation to the pH range of durability of popular compounds engaged in the synthesis/decay of apatites, suggested that the process of the formation of erosion under the influence of acids was much inverted in relation to the process of the formation of apatites, starting from brushite up to apatite, in an alkaline environment. Our simulations showed the shift between the family of bioapatites versus the family of apatites concerning the pH of the reaction environment. The detailed model stoichiometric equations associated with the particular stages of relevant processes were derived. The synthesis processes were alkalization reactions coupled with dehydration. The erosion processes were acid hydrolysis reactions. Formally, the alkalization of the environment during apatite synthesis is presented by introducing Ca(OH) to stoichiometric equations.
本研究主要集中在釉质和牙本质的酸蚀上。对 X 射线衍射数据的详细检查证明,酸引起的釉质衰变产物属于同构生物磷灰石家族,特别是缺钙羟磷灰石。它们正朝着结晶物质越来越少的方向发展。布拉格参数 d 的增加和变化所需能量的减少与 pH 值的变化有关。这对于 pH 值大于 3.5 的酸溶液的腐蚀性作用是有效的。当通过 X 射线衍射研究天然牙齿老化过程时,揭示了与牙齿腐蚀过程明显的相似性。关于骨质疏松骨骼的稀缺数据似乎证实了牙齿得出的结论。有关生物磷灰石衰变的数据与磷灰石合成/衰变的循环相对抗。化学研究主要涉及 Ca/P 比与参与磷灰石合成/衰变的常用化合物耐用性的 pH 值范围有关,表明在酸的影响下形成腐蚀的过程与在碱性环境中从 brushite 到磷灰石形成磷灰石的过程相比,发生了很大的反转。我们的模拟表明,在反应环境的 pH 值方面,生物磷灰石家族与磷灰石家族之间存在转变。推导出了与相关过程特定阶段相关的详细模型化学计量方程。合成过程是与脱水偶联的碱化反应。侵蚀过程是酸水解反应。从形式上讲,在磷灰石合成过程中,环境的碱化是通过向化学计量方程中引入 Ca(OH)来表示的。