Department of Pediatric and Preventive Dentistry, JSS Dental College and Hospital, JSS Academy of Higher Research, Mysuru, Karnataka, India.
J Indian Soc Pedod Prev Dent. 2020 Oct-Dec;38(4):355-360. doi: 10.4103/JISPPD.JISPPD_181_20.
The purpose of the study was to understand the mineral loss in primary and permanent enamel samples and an attempt is made to standardize the process of chemical demineralization to generate more meaningful results in research studies involving the remineralization of demineralized samples.
Due to variability among enamel samples theoretically, it is impossible to standardize demineralization by running time-based chemical demineralization cycle without frequent monitoring. Instead of carrying out demineralization cycles for a fixed duration of time, we quantified the mineral loss 24 hourly using the International Caries Detection and Assessment System (ICDAS) and Quantitative Light-induced Fluorescence System (QLF™). Twenty primary and permanent enamel samples were subjected to demineralization, and ICDAS and QLF™ evaluation were done at 0, 24, 48, 72, 96, 120, 144, and 168 h of demineralization.
The first visual change in permanent enamel is appreciated at 24 h (ICDAS II code1, QLF™ code1 -16.353 - ΔF) of demineralization, at 48 h (ICDAS II code2, QLF™ code2, -24.515 - ΔF), there was localized white spot lesion in permanent enamel and remained until 96 h (ICDAS II code 2, QLF™ code 2, -25.739 - ΔF) of demineralization. In primary samples, distinct visual change was seen at 24 h (ICDAS II code2, QLF™ code2, -19.431 - ΔF), and at 48 h clinically, there was a distinct visual change, but optically mild enamel breakdown was appreciated (ICADSII code 2 QLF™ code3, -27.201 - ΔF), which remained constant till 120 h of demineralization (ICDAS II code2 QLF™ code3 -37.645 - ΔF).
Different samples demineralize at different rates. The demineralization in primary samples was 1.25 times higher than permanent samples. Recommendation: due to inherent variability in the samples continuous monitoring of the demineralization process on a 24 hourly basis is required to standardize the process.
本研究旨在了解原发性和永久性釉质样本的矿物质损失,并尝试标准化化学脱矿过程,以生成更有意义的研究结果,这些研究涉及脱矿样本的再矿化。
由于釉质样本理论上存在变异性,如果不频繁监测,基于时间的化学脱矿循环无法标准化脱矿。因此,我们没有进行固定时间的脱矿周期,而是使用国际龋病检测和评估系统(ICDAS)和定量光致荧光系统(QLF™)每 24 小时定量测量矿物质损失。对 20 个原发性和永久性釉质样本进行脱矿处理,并在脱矿 0、24、48、72、96、120、144 和 168 小时时进行 ICDAS 和 QLF™评估。
永久性釉质的第一个肉眼可见变化发生在脱矿 24 小时(ICDAS II 代码 1,QLF™ 代码 1-16.353-ΔF),在 48 小时(ICDAS II 代码 2,QLF™ 代码 2,-24.515-ΔF),出现局部白垩斑病变,直到 96 小时(ICDAS II 代码 2,QLF™ 代码 2,-25.739-ΔF)。在原发性样本中,在 24 小时(ICDAS II 代码 2,QLF™ 代码 2,-19.431-ΔF)时出现明显的肉眼可见变化,在 48 小时时,肉眼可见有明显的变化,但光学上轻微的牙釉质破裂被认为是(ICADSII 代码 2 QLF™ 代码 3,-27.201-ΔF),直到 120 小时的脱矿过程保持不变(ICDAS II 代码 2 QLF™ 代码 3-37.645-ΔF)。
不同的样本脱矿速度不同。原发性样本的脱矿速度是永久性样本的 1.25 倍。建议:由于样本存在固有变异性,需要连续 24 小时监测脱矿过程,以标准化该过程。