Tukiainen H, Silvasti M, Karttunen P, Savolainen K, Kokkonen P, Parviainen M
Department of Pulmonary Diseases, University of Kuopio, Tarinaharju, Finland.
Int J Clin Pharmacol Ther Toxicol. 1988 Jul;26(7):346-50.
We have compared the pharmacokinetic properties of a slow-release theophylline-hydroxyzine combination and a slow-release theophylline preparation both after a single dose administration and at steady state after the dosage of twice/day for four days in ten healthy volunteers. After a single dose, theophylline was absorbed slightly faster from the combination preparation (Retafyllin comp.) than from a plain theophylline preparation (Theo-Dur). However, in a steady state phase the pharmacokinetic profiles were quite similar. Hydroxyzine showed a slight delay in absorption from the combination preparation, but in a steady state the overall pharmacokinetic profile of hydroxyzine was similar to that of theophylline. Cumulation of either hydroxyzine or theophylline was not evident. On the basis of the present study, the slow-release combination preparation of theophylline and hydroxyzine seems suitable for twice/day dosage.
我们在10名健康志愿者中比较了缓释型氨茶碱-羟嗪组合制剂和缓释型氨茶碱制剂单次给药后的药代动力学特性,以及在每日两次给药、连续四天后的稳态药代动力学特性。单次给药后,氨茶碱从组合制剂(Retafyllin comp.)的吸收略快于普通氨茶碱制剂(Theo-Dur)。然而,在稳态阶段,药代动力学曲线相当相似。羟嗪从组合制剂的吸收略有延迟,但在稳态时,羟嗪的整体药代动力学曲线与氨茶碱相似。羟嗪或氨茶碱均未出现明显蓄积。基于本研究,氨茶碱和羟嗪的缓释组合制剂似乎适合每日两次给药。