Fuchs C, Férault-Larue D H, Heimann G
Arzneimittelforschung. 1980;30(2):333-5.
Three different preparations containing 1 mg fluoride were given to 12 volunteers: preparation A, 1 hydrous solution, = 1 mg F-/100 ml, preparation B = 2 tablets at 0.5 mg F- and preparation C = 1NaF tablet with 1 mg F-. Representactive kinetic data could be obtained by means of restricted fluoride in the diet, a reproducible method yielding minimum detectable fluoride concentration and selection of suitable volunteers.. The enteral absorption of fluoride from solution A was more rapid (half-life of invasion = 20.2 min and 16.9 min, respectively). The delayed release is a consequence of the galenic mixture. In addition, the maximum concentration in plasma was greater and was reached sooner in preparation A when compared to the other preparations. In contrast, there was no difference in the areas under the curves, indicating that the relative bioavailability of fluoride is the same in all preparations.
给12名志愿者服用了三种不同的含1毫克氟化物的制剂:制剂A,1种水溶液,即1毫克氟离子/100毫升;制剂B,2片每片含0.5毫克氟离子的片剂;制剂C,1片含1毫克氟离子的氟化钠片剂。通过限制饮食中的氟化物、一种可重现的产生最低可检测氟化物浓度的方法以及选择合适的志愿者,能够获得代表性的动力学数据。溶液A中氟化物的肠内吸收更快(侵入半衰期分别为20.2分钟和16.9分钟)。延迟释放是药剂混合物的结果。此外,与其他制剂相比,制剂A的血浆最大浓度更高且达到得更快。相比之下,曲线下面积没有差异,表明所有制剂中氟化物的相对生物利用度相同。