Chu I, Villeneuve D C, Secours V, Becking G C, Viau A, Benoit F
Drug Metab Dispos. 1979 Jan-Feb;7(1):24-7.
The absorption, distribution, and excretion of photomirex were investigated in the rat. Photomirex was absorbed slowly after oral administration, appeared in the blood at 1.5 hr, and reached the peak concentration 4 hr after dosing. Elimination from the blood was studied in rats receiving single intravenous doses; the semilog-arithmic decay curve was found to be triphasic. The highest concentrations were present in the rat, liver, and skin. Approximately 38--42% of the orally dosed photomirex was excreted in the feces in the first 3 days and 51--55% was eliminated in 28 days. Only trace amounts of photomirex were found in the urine (less than 0.09% of the total dose in 24 hr). Photomirex constituted about 95% of the total radioactivity found in the tissues and feces. No metabolite was detected in the radioactive material extracted from tissues or feces.
对大鼠体内灭蚁灵的吸收、分布和排泄情况进行了研究。口服给药后,灭蚁灵吸收缓慢,给药1.5小时后出现在血液中,给药4小时后达到峰值浓度。对接受单次静脉注射剂量的大鼠进行了血液消除研究;发现半对数衰减曲线呈三相。大鼠的肝脏和皮肤中浓度最高。口服给药的灭蚁灵约38%-42%在头3天随粪便排出,51%-55%在28天内消除。尿液中仅发现痕量灭蚁灵(24小时内低于总剂量的0.09%)。灭蚁灵约占组织和粪便中总放射性的95%。从组织或粪便中提取的放射性物质中未检测到代谢物。