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经口和静脉给予啮齿动物后,地下水中污染物环丁砜的毒代动力学和生物利用度:剂量、物种和性别比较。

Toxicokinetics and bioavailability of sulfolane, a ground water contaminant, following oral and intravenous administration in rodents: A dose, species, and sex comparison.

机构信息

Division of the National Toxicology Program, National Institute of Environmental Health Sciences, Research Triangle Park, NC, United States of America.

RTI International, Discovery Sciences, Research Triangle Park, NC, United States of America.

出版信息

Toxicol Appl Pharmacol. 2019 Sep 15;379:114690. doi: 10.1016/j.taap.2019.114690. Epub 2019 Jul 22.

Abstract

Sulfolane is a ground water contaminant near refinery sites. The objective of this work was to investigate the toxicokinetics and bioavailability of sulfolane in male and female Harlan Hsd:Sprague Dawley® SD® rats and B6C3F1/N mice following a single oral administration of 10, 30, or 100 mg/kg. Sulfolane was rapidly absorbed in rats with the maximum plasma concentration, C, reached at ≤1.47 h. Although C increased proportionally to the dose, the half-life of elimination increased with the dose and the area under the concentration versus time curve (AUC) increased more than proportionally to the dose. In male and female rats, plasma elimination half-life increased with the dose from 1.97 to 6.33 h. Absorption of sulfolane in mice following oral administration was more rapid than in rats with C reached at ≤0.55 h. In addition, mice had a shorter half-life (≤ 1.25 h) and a lower AUC than rats. In male and female mice, both C and AUC increased more than proportionally to the dose. Bioavailability of sulfolane was higher in rats (81-83%) than mice (59-63%) at 10 mg/kg; at 30 and 100 mg/kg, bioavailability >100% in both species and sexes suggesting that the saturation of metabolism and clearance processes of sulfolane may begin at a single oral dose of ~30 mg/kg. There was no apparent sex difference in toxicokinetic parameters of sulfolane in rats and mice. These data demonstrate that sulfolane was well-absorbed following oral administration with high bioavailability in rats and mice with some species differences, but no sex difference.

摘要

四氢呋喃是炼油厂附近的地下水污染物。本研究的目的是调查雄性和雌性哈兰 Hsd:Sprague Dawley® SD®大鼠和 B6C3F1/N 小鼠单次口服 10、30 或 100mg/kg 后四氢呋喃的毒代动力学和生物利用度。四氢呋喃在大鼠中被迅速吸收,最大血浆浓度 C 在 ≤1.47h 时达到。虽然 C 与剂量成正比增加,但消除半衰期随剂量增加而增加,并且浓度与时间曲线下面积(AUC)与剂量不成比例地增加。在雄性和雌性大鼠中,随着剂量的增加,血浆消除半衰期从 1.97 增加到 6.33h。口服后,小鼠中四氢呋喃的吸收比大鼠更快,C 在 ≤0.55h 时达到。此外,与大鼠相比,小鼠的半衰期更短(≤1.25h),AUC 更低。在雄性和雌性小鼠中,C 和 AUC 均与剂量不成比例地增加。在 10mg/kg 时,四氢呋喃在大鼠中的生物利用度(81-83%)高于小鼠(59-63%);在 30 和 100mg/kg 时,两种物种和性别中的生物利用度均>100%,表明代谢和清除过程可能在单次口服约 30mg/kg 时开始饱和。在大鼠和小鼠中,四氢呋喃的毒代动力学参数没有明显的性别差异。这些数据表明,四氢呋喃口服后吸收良好,在大鼠和小鼠中具有较高的生物利用度,存在一些种属差异,但无性别差异。

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