Iwai H, Wada O, Arakawa Y, Ono T
J Toxicol Environ Health. 1982 Jan;9(1):41-9. doi: 10.1080/15287398209530140.
The intestinal uptake site, enterohepatic circulation, and excretion into bile, feces, and urine of alkyltins (tetra and trialkyltin) were investigated after oral, sc, or intestinal administration of the compounds to rats and rabbits. Assays of tetra- and trialkyltins in biological materials were carried out by gas chromatography. The main uptake sites in the small intestine were the jejunum and duodenum for tetraalkyltins and the ileum and jejunum for trialkyltins. Tetra- and trialkyltins were detected in the small intestine and contents of the intestinal lumen after sc injection of these compounds in rats. These facts suggest that tetra- and trialkyltins are transported in the body through enterohepatic circulation. The route, rate, and amount of excretion of tetra and trialkyltins seem to depend on the velocity of dealkylation, doses, physical and chemical properties, and route of administration of the compounds.
在给大鼠和兔子经口、皮下或肠道给予烷基锡(四烷基锡和三烷基锡)化合物后,对其肠道吸收部位、肝肠循环以及向胆汁、粪便和尿液中的排泄情况进行了研究。生物材料中四烷基锡和三烷基锡的测定通过气相色谱法进行。小肠中四烷基锡的主要吸收部位是空肠和十二指肠,三烷基锡的主要吸收部位是回肠和空肠。在给大鼠皮下注射这些化合物后,在小肠和肠腔内容物中检测到了四烷基锡和三烷基锡。这些事实表明,四烷基锡和三烷基锡通过肝肠循环在体内转运。四烷基锡和三烷基锡的排泄途径、速率和量似乎取决于脱烷基化速度、剂量、物理和化学性质以及化合物的给药途径。