使用每日处方局部氟化物剂对唾液中可用氟化物浓度的比较评估。

Manjit Talwar, Amrit Tewari, H S Chawla, Vinod Sachdev
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引用次数: 6

摘要

目的:评估使用含氟漱口水和牙膏后唾液中氟浓度的可用性。材料与方法:实验对象为昌迪加尔市7-15岁学龄儿童(n = 90)。这些儿童不使用氟化物。收集基线唾液样本。受试者暴露于含氟漱口水(0.05%,225 ppm F)和牙膏(1000 ppm F)两种测试剂中7天,第8天,在20小时内收集唾液样本。在受试者暴露于第二种测试剂之前,有3(1/2)个月的洗脱期。采用氟化物离子特异性电极对唾液中的氟化物进行了测定。取得书面知情同意书。统计分析:采用Kolmogorov-Smirnov检验检验变量的正态性。使用曼-惠特尼u型检验比较了在使用两种测试剂后不同时间间隔唾液中可获得的氟化物浓度。结果:与两种测试剂的基线相比,唾液中的氟化物浓度升高。含氟漱口水(0.05%氟化钠[NaF])和牙膏(1000ppm单氟磷酸盐[MFP])显示出双相清除。唾液高峰出现在使用后15分钟。与基线相比,夜间使用导致唾液中的氟化物浓度更高。在使用后5小时、10小时和20小时,唾液中用于牙齿的氟化物浓度有统计学意义(P < 0.05)。结论:在每日使用NaF(0.05%)漱口水和MFP牙膏(1000 ppm)后,唾液中的氟化物浓度与基线(0.03 ppm)相比,在使用后20小时内,漱口水和牙膏中的氟化物浓度仍然升高到0.12 ppm和0.14 ppm。预防脱矿的治疗窗口虽然尚未确定,但建议为0.1-1 ppm,这表明日常使用含氟漱口水和牙膏可以提供唾液中的氟化物浓度,以预防脱矿。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A comparative assessment of fluoride concentration available in saliva using daily prescribed topical fluoride agents.

A comparative assessment of fluoride concentration available in saliva using daily prescribed topical fluoride agents.

A comparative assessment of fluoride concentration available in saliva using daily prescribed topical fluoride agents.

A comparative assessment of fluoride concentration available in saliva using daily prescribed topical fluoride agents.

Objective: To assess the availability of fluoride concentration in saliva following the use of fluoride mouthrinse and dentifrice.

Materials and methods: The experiment was carried out in 7-15 year-old school children of Chandigarh (n = 90). The children were nonfluoride users. Baseline saliva samples were collected. The subjects were exposed to two test agents, i.e., fluoride mouthrinse (0.05%, 225 ppm F) and dentifrice (1000 ppm F) for 7 days and on the day 8, saliva samples were collected over a 20 hrs period. Wash out period of 3(1/2) months was there before the subjects were exposed to the second test agent. Fluoride in saliva was estimated using fluoride ion-specific electrode. Written informed consent was taken.

Statistical analysis: Kolmogorov-Smirnov test was applied to test the normality of the variables. Mann-Whitney U-test was used to compare the fluoride concentration available in saliva at respective time intervals subsequent to use of the two test agents.

Results: Fluoride concentration was elevated in saliva compared to baseline for both the test agents. Fluoride mouthrinse (0.05% sodium fluoride [NaF]) and dentifrice (1000 ppm monofluorophosphate [MFP]) showed a biphasic clearance. Peak in saliva occurred at 15 mins postuse. Night-time use resulted in higher concentration of fluoride in saliva compared to baseline. There was statistically significantly higher fluoride concentration available in saliva for the dentifrice at 5 hrs, 10 hrs, and 20 hrs postuse (P < 0.05).

Conclusion: Subsequent to the use of NaF (0.05%) daily mouthrinse and MFP dentifrice (1000 ppm) the fluoride concentration in saliva remained elevated to a level of 0.12 ppm for mouthrinse and 0.14 ppm for dentifrice compared to baseline (0.03 ppm) up to 20 hrs postuse. The therapeutic window though not yet established but suggested is 0.1-1 ppm for prevention of demineralization, indicating that daily use of fluoride mouthrinse and dentifrice provides fluoride concentration in saliva for the prevention of demineralization.

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