Gandini R, Assereto R, Castoldi D, Cunietti E, Garanzelli P, Monzani W
Int J Clin Pharmacol Res. 1987;7(2):149-55.
In this study the pharmacokinetics of a new slow-release formulation of bezafibrate (a hypolipaemic drug) were evaluated in a group of six healthy volunteers. In the first part of the study the bioavailability of this formulation was compared to the normal preparation of bezafibrate. In the second part of the experiment the possible accumulation was studied. The subjects were administered the slow-release preparation at 08h00 for seven consecutive days. The resulting data indicate that the slow-release formulation shows a lower dispersion of Tmax values. There was an increase of the plasma half-life from 1.9 to 5.5 h, but a possibility of accumulation could be excluded.
在本研究中,对一组6名健康志愿者评估了一种新的苯扎贝特(一种降血脂药物)缓释制剂的药代动力学。在研究的第一部分,将该制剂的生物利用度与苯扎贝特的常规制剂进行了比较。在实验的第二部分,研究了可能的蓄积情况。受试者于08:00连续7天服用缓释制剂。所得数据表明,缓释制剂的达峰时间(Tmax)值离散度较低。血浆半衰期从1.9小时增加到5.5小时,但可以排除蓄积的可能性。