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大鼠口服 N-甲基吗啉的母胎毒性

Maternal and fetal toxicity of N-methylmorpholine by oral administration in rats.

作者信息

Sitarek K

机构信息

Department of Toxicology and Carcinogenesis, The Nofer Institute of Occupational Medicine, Lodz, Poland.

出版信息

Teratog Carcinog Mutagen. 1999;19(6):369-76.

Abstract

N-methylmorpholine, which is used as a catalyst in polyurethane foams producing, in solvents, stabilizing agents, and corrosion inhibitors, was administered to female rats by gavage at 100, 200, 600, and 900 mg/kg during organogenesis. It did not exhibit selective toxicity toward the developing conceptus. This compound administered to pregnant females was fetotoxic and teratogenic in the presence of maternal toxicity. N-methylmorpholine induced anophthalmia, internal hydrocephalus, and hydronephrosis but only at one dose which was also maternotoxic. Teratogenesis Carcinog. Mutagen. 19:369-376, 1999.

摘要

N-甲基吗啉在聚氨酯泡沫生产中用作催化剂,也用于溶剂、稳定剂和腐蚀抑制剂。在器官形成期,以100、200、600和900毫克/千克的剂量通过灌胃给予雌性大鼠。它对发育中的胚胎未表现出选择性毒性。在存在母体毒性的情况下,给予怀孕雌性该化合物具有胚胎毒性和致畸性。N-甲基吗啉诱发了无眼畸形、脑内积水和肾积水,但仅在一个导致母体毒性的剂量下出现。《致畸作用、致癌作用、诱变作用》1999年第19卷:369 - 376页

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