Hiles R A, Birch C G
Drug Metab Dispos. 1978 Mar-Apr;6(2):177-83.
The metabolism and disposition of 14C-TCC (3,4,4'-trichlorocarbanilide) have been evaluated in humans following oral exposure to 2.2 mumol/kg body wt. Fecal elimination (70% of dose) was complete 120 hr after dosing and the urinary excretion (27% of dose) was completed in 80 hr. The maximum plasma level occurred 2.8 hr after dosing and was 3.7 nmol-equivalents of TCC per g of plasma (approximately 1.2 ppm). Biotransformation of TCC was rapid but did not appear to involve splitting of the basic TCC structure. The major plasma metabolites were N- and N'-glucuronides of TCC which were eliminated with t1/2 approximately 2 hr to the urine and 2'-hydroxy-TCC sulfate and 6-hydroxy-TCC sulfate (the o-hydroxy-TCC sulfates) which were removed with t1/2 approximately 20 hr (presumably into the bile). It is concluded that a nonradioactive analytical method based on the urinary excretion of the N-glucuronides would be suitable for the determination of TCC absorption in humans.
在人体口服2.2微摩尔/千克体重的14C-TCC(3,4,4'-三氯碳酰替苯胺)后,对其代谢和处置情况进行了评估。给药后120小时粪便排泄完成(占剂量的70%),80小时尿液排泄完成(占剂量的27%)。给药后2.8小时出现血浆最高水平,为每克血浆3.7纳摩尔当量的TCC(约1.2 ppm)。TCC的生物转化迅速,但似乎不涉及基本TCC结构的裂解。主要的血浆代谢物是TCC的N-和N'-葡糖醛酸苷,其消除半衰期约为2小时,经尿液排出;还有2'-羟基-TCC硫酸盐和6-羟基-TCC硫酸盐(邻羟基-TCC硫酸盐),其消除半衰期约为20小时(可能排入胆汁)。结论是,基于N-葡糖醛酸苷尿液排泄的非放射性分析方法适用于测定人体中TCC的吸收情况。