Griffith F D, Long J E
Am Ind Hyg Assoc J. 1980 Aug;41(8):576-83. doi: 10.1080/15298668091425301.
These studies were conducted to evaluate the potential toxicity of ammonium perfluorooctanoate, a commercial surfactant. They include acute and subchronic feeding studies with rabbits, mice, rats and monkeys as well as in vitro mutagenicity assays with Salmonella typhimurium and Saccharomyces cerevisiae. The compound was non-irritating to the skin and moderately irritating to the eyes of rabbits. The rat oral LD50 was 540 mg/kg; no deaths resulted from a one hour rat inhalation exposure at a nominal concentration of 18.6 mg/L. All in vitro assays were negative. The liver was the target organ in rodents in both the 28 day and 90 day feeding studies with males showing a greater response than females. Serum and liver concentrations of organic fluorine were greater in male than in female rats. In a 90 day oral study in rhesus monkeys the gastrointestinal tract and the reticuloendothelial system were the sites of toxic effects. The gastrointestinal effects were attributed to the potent surface activity of the compound. Histopathological effects wer noted in the spleen, lymph nodes and bone marrow. Unlike the rats, sex related differences were not evident in the monkeys. Toxicological evaluations of ammonium perfluorooctanoate are continuing.
开展这些研究是为了评估一种商业表面活性剂全氟辛酸铵的潜在毒性。研究包括对兔子、小鼠、大鼠和猴子进行急性和亚慢性喂养研究,以及对鼠伤寒沙门氏菌和酿酒酵母进行体外致突变性试验。该化合物对兔子皮肤无刺激性,对眼睛有中度刺激性。大鼠经口半数致死量为540毫克/千克;在名义浓度为18.6毫克/升的情况下,大鼠吸入1小时未导致死亡。所有体外试验均为阴性。在为期28天和90天的雄性啮齿动物喂养研究中,肝脏是靶器官,雄性的反应比雌性更强烈。雄性大鼠血清和肝脏中的有机氟浓度高于雌性。在对恒河猴进行的为期90天的口服研究中,胃肠道和网状内皮系统是毒性作用部位。胃肠道效应归因于该化合物强大的表面活性。在脾脏、淋巴结和骨髓中发现了组织病理学效应。与大鼠不同,在猴子中未观察到明显的性别相关差异。全氟辛酸铵的毒理学评估仍在继续。