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Chlorine Isotopic Composition of Perchlorate in Human Urine as a Means of Distinguishing Among Natural and Synthetic Exposure Sources

机译:人类尿液中高氯酸盐的氯同位素组成作为区分自然和合成暴露源的一种手段

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摘要

Perchlorate (ClO4) is a ubiquitous environmental contaminant with high human exposure potential; it has both natural and man-made sources in the environment. Natural perchlorate forms in the atmosphere from where it deposits onto the surface of Earth, whereas synthetic perchlorate is manufactured as an oxidant for industrial, aerospace, and military applications. Perchlorate exposure can potentially cause adverse health effects in humans by interfering with the production of thyroid hormones through competitively blocking iodide uptake. To control and reduce perchlorate exposure, the contributions of different sources of perchlorate exposure need to be quantified. Thus, we demonstrate a novel approach for determining the contribution of different perchlorate exposure sources by quantifying stable and radioactive chlorine isotopes of perchlorate extracted from composite urine samples from two distinct populations: one in Atlanta, USA and one in Taltal, Chile (Atacama region). Urinary perchlorate from the Atlanta region resembles indigenous natural perchlorate from the southwestern USA [δ37Cl = +4.1 ± 1.0 ‰; 36Cl/Cl = 1811 (± 136) × 10−15], and urinary perchlorate from the Taltal, Chile region is similar to natural perchlorate in nitrate salt deposits from the Atacama Desert of northern Chile [δ37Cl = −11.0 ± 1.0 ‰; 36Cl/Cl = 254 (± 40) × 10−15]. Neither urinary perchlorate resembled the isotopic pattern found in synthetic perchlorate. These results indicate that natural perchlorate of regional provenance is the dominant exposure source for the two sample populations, and that chlorine isotope ratios provide a robust tool for elucidating perchlorate exposure pathways.
机译:高氯酸盐(ClO4 -)是一种普遍存在的环境污染物,具有很高的人体暴露潜能。它在环境中既有天然来源也有人造来源。天然高氯酸盐在大气中形成,并从大气中沉积到地球表面,而合成高氯酸盐则作为氧化剂制造,用于工业,航空航天和军事应用。高氯酸盐的暴露可能通过竞争性地阻断碘化物的吸收而干扰甲状腺激素的产生,从而可能对人类健康产生不利影响。为了控制和减少高氯酸盐的暴露,需要量化不同高氯酸盐暴露来源的贡献。因此,我们展示了一种新方法,可通过量化从两个不同人群的复合尿液样本中提取的高氯酸盐的稳定和放射性氯同位素来确定不同高氯酸盐暴露源的贡献:一个在美国亚特兰大,一个在智利塔拉特(阿塔卡马地区) 。来自亚特兰大地区的尿高氯酸盐类似于美国西南部的天然高氯酸盐[δ 37 Cl = +4.1±1.0‰; 36 Cl / Cl = 1811(±136)×10 −15 ],智利塔尔塔尔地区的高氯酸盐尿液与该地区硝酸盐盐沉积物中的天然高氯酸盐相似。智利北部的阿塔卡马沙漠[δ 37 Cl = -11.0±1.0‰; 36 Cl / Cl = 254(±40)×10 -15 ]。尿液中的高氯酸盐都没有类似于合成高氯酸盐中的同位素模式。这些结果表明,来自两个地区的天然高氯酸盐是两个样本种群的主要暴露源,氯同位素比率为阐明高氯酸盐的暴露途径提供了强有力的工具。

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