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首页> 外文期刊>Archives of Toxicology >Metabolism and elimination of N-ethyl-2-pyrrolidone (NEP) in human males after oral dosage
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Metabolism and elimination of N-ethyl-2-pyrrolidone (NEP) in human males after oral dosage

机译:口服后男性男性中N-乙基-2-吡咯烷酮(NEP)的代谢和消除

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N-Ethyl-2-pyrrolidone (NEP) is an industrial solvent that has been increasingly used to substitute N-methyl-2-pyrrolidone. NEP is under scrutiny in scientific and regulatory committees because of developmental toxic and teratogenic effects in rodents. The two postulated NEP metabolites 5-hydroxy-N-ethyl-2-pyrrolidone (5-HNEP) and 2-hydroxy-N-ethylsuccinimide (2-HESI) have recently been detected in urine samples from the general population. Thus, the toxicokinetic characterization of these biomarkers of NEP exposure in humans is of relevance both in the occupational as well as the environmental field. We orally dosed 20.9 mg NEP to three male volunteers. These volunteers collected all their urine samples over a period of 4 days post dose. In these samples we identified and quantified the above postulated NEP metabolites 5-HNEP and 2-HESI and determined their urinary elimination kinetics and their metabolic conversion factors. After 4 days we recovered 50.7 % of the dose as these two metabolites in urine, 29.1 % as 5-HNEP and 21.6 % as 2-HESI. The largest share of 5-HNEP was excreted within 24 h post dose, while the major share of 2-HESI was excreted on day 2 post dose. We estimated an elimination half-time for 5-HNEP of approx. 7 h and for 2-HESI of approx. 22–27 h. While the elimination of 5-HNEP was basically finished 72 h post dose, significant amounts of 2-HESI were still eliminated after 96 h. Both biomarkers can now be used in human biomonitoring studies to extrapolate from urinary measurements to the NEP dose taken up and thus to evaluate the risk caused by exposure to this chemical.
机译:N-乙基-2-吡咯烷酮(NEP)是一种工业溶剂,已越来越多地用于替代N-甲基-2-吡咯烷酮。由于啮齿动物具有发育毒性和致畸作用,NEP正受到科学和监管委员会的审查。最近在普通人群的尿液样本中检测到两种假定的NEP代谢物5-羟基-N-乙基-2-吡咯烷酮(5-HNEP)和2-羟基-N-乙基琥珀酰亚胺(2-HESI)。因此,这些NEP暴露在人体中的生物标志物的毒代动力学表征在职业领域和环境领域均具有相关性。我们向三名男性志愿者口服了20.9 mg NEP。这些志愿者在给药后4天内收集了所有尿液样本。在这些样品中,我们鉴定并量化了上述假定的NEP代谢物5-HNEP和2-HESI,并确定了它们的排尿动力学和代谢转换因子。 4天后,我们在尿中回收了这两种代谢产物的50.7%的剂量,其中5-HNEP为29.1%,2-HESI为21.6%。 5-HNEP的最大份额在给药后24小时内排出,而2-HESI的主要份额在给药后2天排出。我们估计5-HNEP的消除半衰期约为。 7小时,约2-HESI。 22–27小时虽然5-HNEP的消除在给药后72小时基本完成,但96小时后仍消除了大量的2-HESI。这两种生物标记物现在都可以用于人类生物监测研究,以从尿液测量值推断出所吸收的NEP剂量,从而评估因接触该化学物质而引起的风险。

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