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27-S系列卤化烃油重复口服毒性的测定

The determination of the repeated oral toxicity of halocarbon oil, series 27-S.

作者信息

Kinkead E R, Culpepper B T, Henry S S, Szotak P S, Flemming C D, Kutzman R S, Bruner R H, Wyman J F, Mattie D R

机构信息

NSI Technology Services Corporation, Dayton, Ohio 45431.

出版信息

Toxicol Ind Health. 1990 Jan;6(1):17-32. doi: 10.1177/074823379000600102.

Abstract

Halocarbon 27-S (HC 27-S), a polymer of chlorotrifluoroethylene (CTFE), is used as a lubricating oil for pumps in hyperbaric chambers. Although monomeric CTFE has been shown to produce renal lesions in rats, the toxicity of CTFE polymers have not been investigated. To assess the toxicity of repeated exposure to HC 27-S, three groups (N = 6/group) of male and female Fischer-344 rats were dosed with 2.5 g HC 27-S/kg for 7 or 21 consecutive days. Groups were sacrificed at 7, 21, and 35 days (14 days after the 21-day dosing). Corresponding control groups (N = 6) were dosed with deionized water. Decreased water consumption and urine output were apparent in all test groups. Statistically significant increases in fluoride excretion were noted in 24-hr urine samples assessed periodically during the study. Neurotoxic signs were observed in female rats but not in male rats. Significant increases in liver and kidney weights were seen in all rats, regardless of number of dosing days. The increased fluoride burden in treated animals appeared sufficient to alter bone calcium/phosphate ratios in male rats but not female rats. Gross liver enlargement and hepatocellular cytomegaly indicated that the liver was probably the primary target organ following repeated administration of HC 27-S.

摘要

氟氯碳27-S(HC 27-S)是一种三氟氯乙烯(CTFE)的聚合物,用作高压舱中泵的润滑油。尽管已表明单体CTFE会在大鼠中产生肾脏损伤,但尚未对CTFE聚合物的毒性进行研究。为了评估重复接触HC 27-S的毒性,将三组(每组N = 6)雄性和雌性Fischer-344大鼠连续7天或21天给予2.5 g HC 27-S/kg的剂量。在第7天、21天和35天(21天给药后14天)处死各组动物。相应的对照组(N = 6)给予去离子水。所有测试组均出现饮水量和尿量减少。在研究期间定期评估的24小时尿液样本中,氟排泄量有统计学意义的增加。在雌性大鼠中观察到神经毒性体征,但在雄性大鼠中未观察到。所有大鼠的肝脏和肾脏重量均显著增加,与给药天数无关。处理动物体内增加的氟负荷似乎足以改变雄性大鼠的骨钙/磷比例,但对雌性大鼠没有影响。肝脏肿大和肝细胞巨大症表明,重复给予HC 27-S后,肝脏可能是主要的靶器官。

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