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首页> 外文期刊>Drug and Chemical Toxicology >Subchronic,Reproductive,and Developmental Toxicity of a Fluorotelomer-Based Urethane Polymeric Product
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Subchronic,Reproductive,and Developmental Toxicity of a Fluorotelomer-Based Urethane Polymeric Product

机译:基于氟调聚物的氨基甲酸酯聚合物产品的亚慢性,生殖和发育毒性

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A commercial fluorotelomer-based urethane polymeric dispersion,consisting of polymer,surfactant,and water,was evaluated in subchronic,reproduction,and developmental toxicity studies.The dispersion was administered daily by gavage to rats at dosages of 0,50,250,or 1000 mg polymer/kg/day or with 70 mg/kg/day of the sulfonate surfactant.Dose levels of 0,50,250,or 1000 mg polymer/kg/day were also used for the reproductive and developmental studies.Nasal olfactory epithelial degeneration and necrosis occurred in all dose groups in the 90-day study.Nasal adhesions were observed only in rats administered surfactant alone.Liver-enzyme alterations at 250 and 1000 mg/kg were considered to be potentially adverse effects.The subchronic no-observed-adverse-effects level(NOAEL)was 50 mg/kg.For the reproduction study,rats were dosed for 10 weeks prior to cohabitation and throughout mating,gestation,and lactation.There were no effects on reproductive function in males or females at any dosage.Thyroid weight was decreased in the 250 and 1000 mg/kg day F1 groups unaccompanied by microscopic effects.In the developmental toxicity study,female rats were dosed from gestation days 6-20;there was no test-substance-related embryolethality,nor was there any dose-related increase in either fetal malformations.Fetal weight was minimally decreased at 1000 mg/kg/day in the presence of slight maternal toxicity;the NOAEL for developmental parameters was 250 mg/kg/day.The polymeric product was not a specific developmental or reproductive toxin.
机译:在亚慢性,生殖和发育毒性研究中对由聚合物,表面活性剂和水组成的基于氟调聚物的氨基甲酸酯聚合物分散体进行了评估。每天通过管饲法以0,50,250或1000 mg聚合物的剂量对大鼠给药该分散体/ kg / day或含70 mg / kg / day的磺酸盐表面活性剂.0,50,250或1000 mg聚合物/ kg / day的剂量水平也用于生殖和发育研究。鼻嗅上皮变性和坏死发生于90天研究中的所有剂量组。仅在单独使用表面活性剂的大鼠中观察到鼻粘连,认为250和1000 mg / kg的肝酶改变可能具有潜在的不良反应。 (NOAEL)为50 mg / kg。在生殖研究中,大鼠在同居前以及整个交配,妊娠和哺乳期给药10周。任何剂量对雄性或雌性的生殖功能均无影响。在250和1000 mg / kg体重的F1组,体重没有减轻,没有微观影响。在发育毒性研究中,从妊娠6-20天开始给予雌性大鼠;没有与试验物质有关的胚胎致死率,也没有两种胎儿畸形的剂量相关性增加。在有轻微母体毒性的情况下,胎儿体重在1000 mg / kg / day时最小降低;发育参数的NOAEL为250 mg / kg / day。或生殖毒素。

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