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Distribution of PCBs, Their Hydroxylated Metabolites, and Other Phenolic Contaminants in Human Serum from Two European Countries

机译:来自两个欧洲国家的人血清中PCBs,其羟基化代谢产物和其他酚类污染物的分布

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摘要

Human exposure to mixtures of polychlorinated biphenyls (PCBs) may result in the formation of different profiles of hydroxylated PCBs (HO-PCBs), as a consequence of different exposures or dissimilar metabolism of parent compounds. Therefore, we investigated the levels and profiles of PCBs and HO-PCBs in human serum samples collected from two European countries with different degrees of pollution. There was no significant difference between the levels of sum PCBs measured in each set of samples, with a median concentration of 3100 pg/mL for Romanian samples (n = 53) and 3380 pg/mL for Belgian samples (n = 22). However, the median concentrations recorded for sum HO-PCBs were almost double in Belgian (310 pg/mL) compared to Romanian (175 pg/mL) samples. The detection frequency recorded for HO-PCBs in Belgian samples was also significantly higher compared to Romanian samples. The main contributors to the sum HO-PCBs in the Belgian samples were 4HO-CB107 > 4HO-CB146 > 4HO-CB187 (76% from the sum HO-PCBs) and 4HO-CB187 > 4HO-CB146 > 3'HO-CB138 (66% from the sum of HO-PCBs) in the Romanian samples. The HO-PCB profile showed that the higher chlorinated HO-PCBs had a higher contribution in the Romanian samples compared to the Belgian ones. This suggests that differences in the PCB profiles between populations can lead to the formation of different HO-PCB metabolite profiles presenting thus different risks for populations. No clear preferentialrnmechanism of HO-PCB metabolite formation (HO-direct insertion vs. 1,2-shift of a chlorine atom) could be highlighted for investigated samples. The main chlorinated phenolic compound found in the Belgian samples was pentachlorophenol (PCP) which accounted for up to 85% of the total quantified phenolics, whereas in the Romanian samples, PCP accounted for only 35%.
机译:人类暴露于多氯联苯(PCB)的混合物可能会导致母体化合物的暴露程度不同或代谢不同,从而导致羟化PCB(HO-PCBs)形成不同的轮廓。因此,我们调查了从两个污染程度不同的欧洲国家采集的人血清样品中PCBs和HO-PCBs的水平和概况。在每组样品中测量的总PCB含量之间没有显着差异,罗马尼亚样品(n = 53)的中位数浓度为3100 pg / mL,比利时样品(n = 22)的中位数浓度为3380 pg / mL。但是,与罗马尼亚样品(175 pg / mL)相比,比利时(310 pg / mL)的总HO-PCBs记录的中值浓度几乎翻了一番。与罗马尼亚样品相比,比利时样品中HO-PCBs记录的检测频率也明显更高。比利时样本中HO-PCB总量的主要贡献者是4HO-CB107> 4HO-CB146> 4HO-CB187(占HO-PCB总量的76%)和4HO-CB187> 4HO-CB146> 3'HO-CB138(罗马尼亚样品中HO-PCBs的总含量的66%。 HO-PCB的分布图表明,与比利时的样品相比,罗马尼亚样品中较高氯化的HO-PCB的贡献更大。这表明人群之间PCB分布的差异可能导致形成不同的HO-PCB代谢物分布,从而给人群带来了不同的风险。对于研究的样品,HO-PCB代谢物的形成没有明确的优先机制(HO直接插入与氯原子的1,2-移位)。比利时样品中发现的主要氯化酚类化合物是五氯苯酚(PCP),最多占定量酚类总量的85%,而在罗马尼亚样品中,PCP仅占35%。

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  • 来源
    《Environmental Science & Technology》 |2010年第8期|p.2876-2883|共8页
  • 作者单位

    Toxicological Center, Department of Pharmaceutical Sciences, University of Antwerp, Universiteitsplein 1, 2610 Wilrijk, Belgium Department of Chemistry, 'Al. I. Cum' University of Iasi, Carol I Bvd. No 11, 700506 Iasi, Romania;

    Department of Biology, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Antwerp (Wilrijk), Belgium;

    Department of Chemistry, 'Al. I. Cum' University of Iasi, Carol I Bvd. No 11, 700506 Iasi, Romania;

    Toxicological Center, Department of Pharmaceutical Sciences, University of Antwerp, Universiteitsplein 1, 2610 Wilrijk, Belgium;

    Toxicological Center, Department of Pharmaceutical Sciences, University of Antwerp, Universiteitsplein 1, 2610 Wilrijk, Belgium Laboratory for Ecophysiology, Biochemistry and Toxicology, Department of Biology, University of Antwerp, Groenenborgerlaan 171, 2020 Antwerp, Belgium;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-17 14:03:58

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