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Evaluation of a new intraoral controlled fluoride release device.

机译:评估一种新型的口腔内氟化物释放装置。

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The aim of the study was to determine the pharmacokinetics of a new hydroxyapatite-Eudragit RS100 diffusion-controlled fluoride-releasing system designed for intraoral use with a 0.15 mg F(-)/day release for a 1-month period. Matrix tablets, each containing 18 mg of sodium fluoride, were bonded to the buccal surface of the first maxillary molar teeth of 20 subjects (age 20-23 years). Morning and evening salivary and urinary samples were collected 5 days before the study and every day for the 1st week, then once a week for 1 month. Fluoride ion measurements were done using the microdiffusion method. The salivary and urinary fluoride concentrations were significantly raised during the treatment period (p < 0.05). Morning salivary fluoride levels were higher than evening salivary fluoride levels (p < 0.05) whereas evening urinary fluoride levels were higher than morning urinary fluoride levels (p < 0.05). The statistically significant increase in salivary fluoride levels indicates a caries-preventive rolefor this device. Copyright (c) 2005 S. Karger AG, Basel.
机译:这项研究的目的是确定一种新的羟基磷灰石-Eudragit RS100扩散控制氟释放系统的药代动力学,该系统设计用于口服,口服剂量为0.15 mg F(-)/天,持续1个月。将每个包含18 mg氟化钠的基质片剂粘合到20位受试者(年龄20-23岁)的第一颗上颌磨牙的颊面。在研究前5天和第1周每天收集早,晚唾液和尿液样本,然后每周一次,共1个月。氟离子的测量使用微扩散法进行。在治疗期间唾液和尿中氟化物的浓度显着升高(p <0.05)。早上唾液中的氟化物水平高于晚上唾液中的氟化物水平(p <0.05),而晚上尿液中的氟化物水平高于早上唾液中的氟化物水平(p <0.05)。唾液中氟化物水平的统计显着增加表明该设备的防龋作用。版权所有(c)2005 S.Karger AG,巴塞尔。

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