Microbead beating extraction of avian eggs for polycyclic aromatic compounds

被引:0
|
作者
Xia Z. [1 ]
Idowu I. [1 ]
Halldorson T. [1 ]
Lucas A.-M. [1 ]
Stein C. [1 ]
Kaur M. [1 ]
Tomy T. [1 ]
Marvin C. [2 ]
Thomas P.J. [3 ]
Hebert C.E. [3 ]
Smith R.A. [4 ]
Dwyer-Samuel F. [5 ]
Provencher J.F. [3 ]
Tomy G.T. [1 ]
机构
[1] University of Manitoba, Department of Chemistry, Winnipeg, R3T 2N2, MB
[2] Water Science and Technology Directorate, Environment and Climate Change Canada, Burlington, L7S 1A1, ON
[3] Wildlife Landscape Science Directorate, Environment and Climate Change Canada, Ottawa, K1A 0H3, ON
[4] Carleton University, Department of Biology, Ottawa, K1S 5B6, ON
[5] Nunatsiavut Government, Nain, A0P 1L0, NL
基金
加拿大自然科学与工程研究理事会;
关键词
Method validation; Microbead extraction; Polycyclic aromatic compounds; Seabird eggs;
D O I
10.1016/j.chemosphere.2023.139059
中图分类号
学科分类号
摘要
Due to their relatively high trophic position and importance as a food source for many communities in the circumpolar north, seabird eggs are an important matrix for monitoring contaminant levels. In fact, many countries, including Canada, have established long-term seabird egg contaminant monitoring programs, with oil related compounds a contaminant of emerging concern for seabirds in several regions. Current approaches to measuring many contaminant burdens in seabird eggs are time-consuming and often require large volumes of solvent. Here we propose an alternative approach, based on the principle of microbead beating tissue extraction using custom designed stainless-steel extraction tubes and lids, to measure a suite of 75 polycyclic aromatic compounds (polycyclic aromatic hydrocarbons (PAHs), alkyl-PAHs, halogenated-PAHs and some heterocyclic compounds) comprising a wide-range of chemical properties. Our method was conducted in strict accordance with ISO/IEC 17025 guidelines for method validation. Accuracies for our analytes generally ranged from 70 - 120%, and intra and inter-day repeatability for most analytes were < 30%. Limits of detection/quantitation for the 75 target analytes were < 0.2/0.6 ng g−1. The level of contamination in our method blanks was significantly smaller in our stainless-steel tubes/lids relative to commercially available high-density plastic alternatives. Overall, our method meets our data quality objectives and results in a notable reduction in sample processing times relative to current approaches. © 2023 Elsevier Ltd
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