Chu I, Villeneuve D C, Becking G C, Viau A
J Toxicol Environ Health. 1980 Jul;6(4):713-21. doi: 10.1080/15287398009529890.
The tissue distribution and elimination kinetics of 14C-labeled dihydromirex were investigated in the rat. Dihydromirex was distributed in all tissues examined after iv or oral administration; the highest concentrations were found in the fat, liver, and skin. The pattern of distribution was similar to that of photomirex and mirex. Elimination of dihydromirex from the blood after an iv dose was expressed by a four-compartment model, whereas fecal excretion was represented by a biphasic curve. Excretion of dihydromirex occurred predominantly in the feces; only minute amounts were found in the urine and bile. Dihydromirex constituted 90-100% of the total radioactivity in tissues and feces. No metabolite was detected.
在大鼠体内研究了14C标记的狄氏剂的组织分布和消除动力学。静脉注射或口服给药后,狄氏剂分布于所有检测的组织中;脂肪、肝脏和皮肤中的浓度最高。其分布模式与光狄氏剂和狄氏剂相似。静脉注射一剂后,狄氏剂从血液中的消除可用四室模型表示,而粪便排泄则用双相曲线表示。狄氏剂的排泄主要发生在粪便中;尿液和胆汁中仅发现微量。狄氏剂占组织和粪便中总放射性的90 - 100%。未检测到代谢物。