Borrisud M, Alexander M S, Andresen B D
Am J Obstet Gynecol. 1985 Oct 1;153(3):332-4. doi: 10.1016/s0002-9378(85)80126-5.
The metabolism of ritodrine has been studied in the rat, both in vitro and in vivo, and in the in vivo pregnant baboon, with the use of tritium-labeled drug as a probe. Combined enzymatic degradation and radiochromatography of the radioactive components of bile and urine show that ritodrine undergoes significant Phase l metabolism in addition to conjugation to both sulfate and glucuronide, as previously reported. The presence of more than one conjugate is shown, and evidence for major interspecies variation in patterns of metabolism and conjugation is presented, with comments on the applicability of results to human clinical use.
已利用氚标记药物作为探针,在大鼠体内外以及怀孕的狒狒体内研究了利托君的代谢情况。如先前报道,胆汁和尿液放射性成分的联合酶降解和放射色谱分析表明,利托君除了与硫酸盐和葡萄糖醛酸结合外,还经历了显著的I相代谢。研究显示存在不止一种结合物,并呈现了代谢和结合模式存在主要种间差异的证据,同时对研究结果应用于人类临床的适用性进行了评论。