Silva Mayron Guedes, Sousa Klícia Kallynne Cutrim, de Menezes Alan Silva, Firoozmand Leily Macedo
Postgraduate Program in Dentistry, Federal University of Maranhão (UFMA), 65.080-805, São Luís, MA, Brazil.
Department of Dentistry I, Federal University of Maranhão (UFMA), 65.080-805, São Luís, MA, Brazil.
J Dent. 2025 Sep;160:105890. doi: 10.1016/j.jdent.2025.105890. Epub 2025 Jun 6.
To evaluate in vitro the impact of pepsin on enamel erosion in the presence of an acquired pellicle and assess the protective efficacy of a bioactive gel containing surface pre-reacted glass-ionomer (S-PRG) particles by measuring surface hardness loss.
Bovine enamel blocks were prepared, standardized, and randomly assigned to two groups (n = 24/group): HCl-only erosive model and HCl+Pep - an erosive model with pepsin. Each group was further divided into two pre-treatment conditions (n = 12/group): SPRG (exposure to S-PRG bioactive gel) and DW (immersion in deionized water, control). Baseline enamel superficial microhardness was measured. Acquired pellicle was formed using human saliva and the samples were subjected to an erosive challenge for 9 days. Surface hardness loss (%SHL), morphological and mineral composition changes (scanning electron microscopy [SEM]/energy-dispersive X-ray spectroscopy), and crystal characteristics (X-ray diffraction [XRD]) were analyzed. Statistical analysis was performed using one-way analysis of variance (p < 0.05).
The HCl+Pep group exhibited significantly higher %SHL than the HCl-only group (p < 0.001). Pre-treatment with S-PRG gel did not significantly reduce %SHL (p > 0.05). SEM images revealed severe mineral loss in the interprismatic regions of the HCl+Pep/DW group, whereas the HCl/SPRG group exhibited less degradation. XRD analysis indicated modifications in hydroxyapatite (HAp) microstructure, with the formation of octacalcium phosphate, in the HCl/SPRG.
Pepsin exacerbates enamel erosion by increasing %SHL and altering the morphology and structural pattern of HAp crystals. Although S-PRG gel pre-treatment did not prevent %SHL, it facilitated the formation of a new crystalline phase and reduced enamel degradation.
Pepsin exacerbates enamel erosion by intensifying mineral loss despite the acquired pellicle. Although it does not prevent hardness loss, bioactive materials are emerging as a promising supportive strategy - minimizing surface degradation through possible crystal structure modification, particularly in gastroesophageal reflux-related erosion conditions.
在体外评估胃蛋白酶在获得性薄膜存在的情况下对牙釉质侵蚀的影响,并通过测量表面硬度损失来评估含有表面预反应玻璃离子(S-PRG)颗粒的生物活性凝胶的保护效果。
制备、标准化牛牙釉质块,并随机分为两组(每组n = 24):仅用盐酸的侵蚀模型组和添加胃蛋白酶的盐酸侵蚀模型组(HCl+Pep)。每组进一步分为两种预处理条件(每组n = 12):SPRG组(暴露于S-PRG生物活性凝胶)和蒸馏水组(浸入去离子水中,作为对照)。测量牙釉质基线表面显微硬度。使用人唾液形成获得性薄膜,然后将样本进行9天的侵蚀性挑战。分析表面硬度损失(%SHL)、形态和矿物成分变化(扫描电子显微镜[SEM]/能量色散X射线光谱)以及晶体特征(X射线衍射[XRD])。采用单因素方差分析进行统计分析(p < 0.05)。
HCl+Pep组的%SHL显著高于仅用盐酸组(p < 0.001)。用S-PRG凝胶预处理并未显著降低%SHL(p > 0.05)。SEM图像显示,HCl+Pep/蒸馏水组柱间质区域有严重的矿物质损失,而HCl/SPRG组降解程度较小。XRD分析表明,HCl/SPRG组中羟基磷灰石(HAp)微观结构发生改变,形成了磷酸八钙。
胃蛋白酶通过增加%SHL以及改变HAp晶体的形态和结构模式,加剧了牙釉质侵蚀。尽管S-PRG凝胶预处理未能防止%SHL,但它促进了新晶相的形成并减少了牙釉质降解。
尽管存在获得性薄膜,胃蛋白酶仍通过加剧矿物质流失而加重牙釉质侵蚀。虽然生物活性材料不能防止硬度损失,但作为一种有前景的支持策略正在兴起——通过可能的晶体结构改变将表面降解降至最低,特别是在与胃食管反流相关的侵蚀情况下。