Weigel W W, Plotnick H B, Conner W L
Res Commun Chem Pathol Pharmacol. 1978 May;20(2):275-87.
The tissue distribution and excretion of 14C-epichlorohydrin was studied in both male and female rats following an oral dose of 10 mg/kg. Organs containing the highest concentrations of radioactive label per unit weight were the kidneys, liver, pancreas, ann spleen. With the exception of the pancreas, these are the same organs in which epichlorohydrin-induced pathologic changes have been reported by a number of investigators, indicating a direct correlation between tissue levels and target organ toxicity. The principal route of excretion was via the kidneys, 38-40% of the dose appearing in the urine during the 72 hour period of study. Fecal excretion was relatively insignificant, representing less than 4% of the administered dose. It was found that 18-21% of the administered dose appeared as 14CO2 in the expired air, the majority being excreted in the first 4 hours, suggesting a rapid and extensive biotransformation of the compound.
给雄性和雌性大鼠口服剂量为10mg/kg的14C-环氧氯丙烷后,研究了其在大鼠体内的组织分布和排泄情况。单位重量放射性标记物浓度最高的器官是肾脏、肝脏、胰腺和脾脏。除胰腺外,这些器官也是许多研究者报告的环氧氯丙烷诱导病理变化的器官,表明组织水平与靶器官毒性之间存在直接相关性。排泄的主要途径是通过肾脏,在72小时的研究期间,38-40%的剂量出现在尿液中。粪便排泄相对较少,占给药剂量的不到4%。研究发现,18-21%的给药剂量以14CO2的形式出现在呼出气体中,大部分在最初4小时内排出,这表明该化合物发生了快速而广泛的生物转化。