Dias Susana, Mata António, Silveira João, Pereira Ruben, Putignano Angelo, Orsini Giovanna, Monterubbianesi Riccardo, Marques Duarte
Oral Biology and Biochemistry Research Group, Faculdade de Medicina Dentária, Universidade de Lisboa, 1950-044 Lisboa, Portugal.
LIBPhys-FCT UID/FIS/04559/2013, Faculdade de Medicina Dentária, Universidade de Lisboa, 1950-044 Lisboa, Portugal.
Materials (Basel). 2021 Dec 10;14(24):7597. doi: 10.3390/ma14247597.
Tooth whitening efficacy can be influenced by several factors, of which concentration and application time are two of the most important. This in vitro study aimed to evaluate the initial content and release kinetics of the hydrogen peroxide (HP) content, or the carbamide peroxide (CP) content as converted to its HP equivalent, of four tooth whitening products with different concentrations (6% HP, 16% CP, 10% CP, and 5% CP). Titrations with Cerium Sulphate IV were performed to determine HP concentration. HP release kinetics were evaluated by a spectrophotometric technique. The results were expressed as the mean values and 95% confidence interval of the percentage of hydrogen peroxide content during release kinetics. One sample -test, one-way ANOVA, Tukey post hoc testing, and Pearson correlation testing were used, as appropriate, with a significance level of α = 0.05. The concentration of titrated HP was higher than that indicated by the manufacturers in all tested products ( < 0.01). At the minimum application times indicated by the manufacturers, all products released at least 85% of HP content; the gel containing 10% CP registered the lowest release at 85.49 (81.52-89.46). There was a significant HP release in all products during the application times indicated by the manufacturers. Further studies are needed to assess in vitro release kinetics.
牙齿美白效果会受到多种因素影响,其中浓度和作用时间是两个最重要的因素。本体外研究旨在评估四种不同浓度(6%过氧化氢、16%过氧化脲、10%过氧化脲和5%过氧化脲)的牙齿美白产品中过氧化氢(HP)含量或换算为HP当量的过氧化脲(CP)含量的初始含量及释放动力学。采用硫酸铈IV滴定法测定HP浓度。通过分光光度技术评估HP释放动力学。结果以释放动力学过程中过氧化氢含量百分比的平均值和95%置信区间表示。根据情况使用单样本检验、单因素方差分析、Tukey事后检验和Pearson相关性检验,显著性水平α = 0.05。所有受试产品中滴定得到的HP浓度均高于制造商标明的浓度(<0.01)。在制造商标明的最短作用时间时,所有产品至少释放了85%的HP含量;含10% CP的凝胶释放量最低,为85.49(81.52 - 89.46)。在制造商标明的作用时间内,所有产品均有显著的HP释放。需要进一步研究来评估体外释放动力学。