Quantitative and spectroscopic assessment of early-stage enamel erosion induced by popular acidic beverages.

IF 3.1 2区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Fajer AlHelal, Zakiya AlHomaizi, Maryam AlOmair, Lama W Yousef, Muawia A Qudeimat
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引用次数: 0

Abstract

Objective: This study aimed to evaluate the initial effects of Coca-Cola, Red Bull, their sugar-free variants, and bottled orange juice on enamel surface roughness and mineral content.

Methods: Fifty-five sound human premolars were sectioned, mounted in resin, and polished to expose standardized enamel surfaces. After quality control, 75 samples (15 per group) were randomized and immersed in artificial saliva before submersion in acidic beverages (Coca-Cola, Red Bull, their sugar-free variants, and bottled orange juice) for 5 min. Surface roughness (Ra, Rq, Rz, Rv) was measured using optical profilometry, while Fourier Transform Infrared Spectroscopy (FTIR) analysis assessed mineral composition. The pH, titratable acidity, and buffering capacity of the beverages were also evaluated. Statistical analysis included paired t-tests, Wilcoxon signed-rank, Kruskal-Wallis, and ANOVA tests with p < 0.05 considered significant.

Results: Coca-Cola showed the lowest pH (2.36 ± 0.05) while bottled orange juice had the highest (3.68 ± 0.03). Red Bull exhibited the highest titratable acidity (TA) (10.93 ± 1.17 mL NaOH) and buffering capacity (β) (2.97 ± 0.36), followed by orange juice (TA = 10.00 ± 0.40 mL; β = 2.97 ± 0.05). All beverages significantly increased surface roughness parameters (Ra, Rq, Rz; p < 0.05) except Rv for Coca-Cola (∆Rv= -0.23 ± 0.50, p = 0.094) and Coca-Cola Light (∆Rv=-0.34 ± 0.78, p = 0.114). Red Bull caused the greatest roughness changes (∆Ra= -0.12 ± 0.07, p < 0.001). FTIR revealed that Coca-Cola significantly elevated the PO4 signal (ΔPO4 = - 9.996 ± 17.305, p = 0.050), while Coca-Cola Light (∆Amide I = + 9.88 ± 17.39, p = 0.045) and Sugar-Free Red Bull (∆Amide I = + 50.25 ± 46.14, p = 0.001) decreased Amide I FTIR signal. Red Bull altered both PO4 (∆PO4= -1.72 ± 2.15, p = 0.008) and Amide I signals (∆Amide I = + 26.21 ± 37.80, p = 0.018). Orange juice showed no significant changes in any parameter (p > 0.05). Kruskal-Wallis tests confirmed significant differences between-group in post-exposure Amide I, Peak PO4, mineral-to-matrix, and CO3/PO4 ratios (p < 0.05).

Conclusion: This study demonstrates that all tested beverages increased enamel surface roughness within minutes, with energy drinks causing the most severe effects. While colas and energy drinks altered both surface and chemical properties, bottled orange juice affected only surface topography without detectable mineral changes. These distinct erosion patterns suggest that different beverages may require tailored preventive strategies.

流行酸性饮料引起的早期牙釉质侵蚀的定量和光谱评价。
目的:本研究旨在评估可口可乐、红牛及其无糖变体和瓶装橙汁对牙釉质表面粗糙度和矿物质含量的初步影响。方法:对55颗健康的人前磨牙进行切片,用树脂固定,抛光,露出标准的牙釉质表面。在质量控制后,随机选取75个样本(每组15个)浸泡在人工唾液中,然后浸泡在酸性饮料(可口可乐、红牛及其无糖变体和瓶装橙汁)中5分钟。表面粗糙度(Ra, Rq, Rz, Rv)使用光学轮廓术测量,而傅里叶变换红外光谱(FTIR)分析评估矿物成分。还对饮料的pH值、可滴定酸度和缓冲能力进行了评价。统计分析采用配对t检验、Wilcoxon符号秩检验、Kruskal-Wallis检验和带p的方差分析。结果:可口可乐的pH值最低(2.36±0.05),瓶装橙汁的pH值最高(3.68±0.03)。红牛具有最高的可滴定酸度(TA)(10.93±1.17 mL NaOH)和缓冲能力(β)(2.97±0.36),其次是橙汁(TA = 10.00±0.40 mL; β = 2.97±0.05)。所有饮料均显著提高了表面粗糙度参数(Ra、Rq、Rz; p 4信号(ΔPO4 = - 9.996±17.305,p = 0.050),而Coca-Cola Light(∆Amide I = + 9.88±17.39,p = 0.045)和无糖红牛(∆Amide I = + 50.25±46.14,p = 0.001)降低了Amide I FTIR信号。红牛改变了PO4信号(∆PO4= -1.72±2.15,p = 0.008)和Amide I信号(∆Amide I = + 26.21±37.80,p = 0.018)。橙汁各参数无显著变化(p < 0.05)。Kruskal-Wallis测试证实了两组之间在暴露后酰胺I、峰值PO4、矿物质与基质、CO3/PO4比率方面的显著差异(p)。结论:本研究表明,所有被测试的饮料都在几分钟内增加了牙釉质表面的粗糙度,其中能量饮料的影响最为严重。虽然可乐和能量饮料改变了表面和化学性质,但瓶装橙汁只影响表面形貌,没有可检测到的矿物质变化。这些不同的侵蚀模式表明,不同的饮料可能需要量身定制的预防策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Oral Health
BMC Oral Health DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
3.90
自引率
6.90%
发文量
481
审稿时长
6-12 weeks
期刊介绍: BMC Oral Health is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of disorders of the mouth, teeth and gums, as well as related molecular genetics, pathophysiology, and epidemiology.
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