Suppr超能文献

大鼠体内全氟膦酸的摄入和消除。

Uptake and elimination of perfluorinated phosphonic acids in the rat.

机构信息

Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario M5S 3H6 Canada.

出版信息

Environ Toxicol Chem. 2010 Jun;29(6):1319-29. doi: 10.1002/etc.167.

Abstract

The mono- and di-substituted perfluorinated phosphonic acids (mono-PFPAs and di-PFPAs) are high production volume fluorinated surfactants. Mono-PFPAs have been observed in Canadian surface waters and wastewater treatment plant (WWTP) effluent. The first observation of the di-PFPAs in the environment is reported here, with the observation of the C6/C6 and C6/C8 di-PFPAs in the National Institute for Standards and Technology (NIST) WWTP sludge standard reference material (SRM) 2781. To characterize the risk associated with human exposure to the mono-PFPAs and di-PFPAs, we determined uptake and elimination parameters in the rat. After oral gavage all of the mono-PFPA and di-PFPA congeners were observed in the blood of the dosed animals. Half-lives after intraperitoneal dosing ranged from 0.96 +/- 0.11 to 2.8 +/- 0.5 days for the mono-PFPAs and 1.8 +/- 0.1 to 9.3 +/- 1.5 days for the di-PFPAs. These half-lives are of similar magnitude to those for perfluorooctane sulfonate (PFOS, 8 to 30 days in male rats) and perfluorooctanoate (PFOA, 6 days in male rats and 1 hour in female rats). Both PFOS and PFOA have human half-lives on the order of years, and so the mono-PFPAs and di-PFPAs may also have significant lifetimes in the human body. The analysis of paired whole blood and plasma samples demonstrated that the mono-PFPAs may bind to blood cells underestimating their concentration in plasma and sera samples. The biological fate of the mono-PFPAs and di-PFPAs determined here suggest there is the potential for human exposure and that if exposure does occur, they may be long-lived in the body.

摘要

单取代和二取代全氟膦酸(单 PFPAs 和二 PFPAs)是高产量的含氟表面活性剂。单 PFPAs 已在加拿大地表水和废水处理厂(WWTP)废水中被发现。本文首次报道了二 PFPAs 在环境中的存在,在 NIST WWTP 污泥标准参考物质(SRM)2781 中观察到了 C6/C6 和 C6/C8 二 PFPAs。为了描述人类接触单 PFPAs 和二 PFPAs 所带来的风险,我们在大鼠体内测定了它们的吸收和消除参数。经口服灌胃后,所有的单 PFA 和二 PFA 同系物都在给药动物的血液中被检测到。经腹腔给药后,单 PFPAs 的半衰期范围为 0.96 +/- 0.11 至 2.8 +/- 0.5 天,二 PFPAs 的半衰期范围为 1.8 +/- 0.1 至 9.3 +/- 1.5 天。这些半衰期与全氟辛烷磺酸(PFOS,雄性大鼠 8-30 天)和全氟辛酸(PFOA,雄性大鼠 6 天,雌性大鼠 1 小时)相似。PFOS 和 PFOA 在人体内的半衰期均为数年,因此单 PFPAs 和二 PFPAs 也可能在人体内有很长的寿命。对配对全血和血浆样本的分析表明,单 PFPAs 可能与血细胞结合,从而低估了其在血浆和血清样本中的浓度。本文确定的单 PFPAs 和二 PFPAs 的生物学命运表明,人类有接触它们的潜在风险,如果接触确实发生,它们可能在体内长期存在。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验