Polychlorinated naphthalenes (PCNs) in food and humans

被引:86
作者
Fernandes, Alwyn [1 ]
Rose, Martin [1 ]
Falandysz, Jerzy [2 ]
机构
[1] Fera Sci Ltd, York YO41 1LZ, N Yorkshire, England
[2] Gdansk Univ, Lab Environm Chem & Ecotoxicol, Gdansk, Poland
关键词
Congener-specific; Dietary exposure; Fish; Relative potencies; Toxic equivalence; DIBENZO-P-DIOXINS; POLYCYCLIC AROMATIC-HYDROCARBONS; HUMAN ADIPOSE-TISSUE; SWEDISH HUMAN-MILK; CHLORINATED NAPHTHALENES; RISK-ASSESSMENT; ORGANOCHLORINE CONTAMINANTS; DEVELOPMENTAL TOXICITY; RELATIVE POTENCIES; MASS-SPECTROMETRY;
D O I
10.1016/j.envint.2017.02.015
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Polychlorinated naphthalenes (PCNs) are legacy contaminants that are listed by the Stockholm convention, initially for reduction of inadvertent production and ultimately, for elimination. They originate through releases from older electrical equipment, inadvertent contamination in industrial chemicals and from combustion processes such as incineration. Recent advances in measurement techniques have allowed a greater characterisation of PCN occurrence, yielding more specific data including individual PCN congener concentrations. Emerging data on food shows widespread occurrence in most commonly consumed foods from different parts of the world. Concurrently, toxicological studies have also allowed a greater insight into the potencies of some congeners, a number of which are known to elicit potent, aryl hydrocarbon receptor (AhR) mediated responses, often referred to as dioxin-like toxicity. The dietary pathway is widely recognised as the most likely route to nonoccupational human exposure. This paper reviews some of the more recent findings on PCN occurrence in food, biota, and human tissues, and discusses the use of relative potencies to express PCN toxicity in foods.
引用
收藏
页码:1 / 13
页数:13
相关论文
共 107 条
  • [1] Dioxin like compounds from municipal waste incinerator emissions: Assessment of the presence of polychlorinated naphthalenes
    Abad, E
    Caixach, J
    Rivera, J
    [J]. CHEMOSPHERE, 1999, 38 (01) : 109 - 120
  • [2] Aittola J.-P., 1994, ORGANOHALOGEN COMPOU, V19, P321
  • [3] [Anonymous], ORGANOHALOGEN COMPD
  • [4] [Anonymous], 34 IPCS WHO
  • [5] [Anonymous], 2001, 34 CICAD
  • [6] ARNOT J, 2003, QUANT STRUCT-ACT REL, V22, P1
  • [7] Action of Halowax 1051 on Enzymes of Phase I (CYP1A1) and Phase II (SULT1A and COMT) Metabolism in the Pig Ovary
    Barc, Justyna
    Karpeta, Anna
    Gregoraszczuk, Ewa Lucja
    [J]. INTERNATIONAL JOURNAL OF ENDOCRINOLOGY, 2013, 2013
  • [8] Brominated dioxin-like compounds: in vitro assessment in comparison to classical dioxin-like compounds and other polyaromatic compounds
    Behnisch, PA
    Hosoe, K
    Sakai, S
    [J]. ENVIRONMENT INTERNATIONAL, 2003, 29 (06) : 861 - 877
  • [9] Bell W. B., 1953, Veterinary Medicine, V48, P135
  • [10] Blankenship A., 1999, ORGANOHAL COMP, V42, P217