Quantification of 13 priority polycyclic aromatic hydrocarbons in human urine by headspace solid-phase microextraction gas chromatography-isotope dilution mass spectrometry

被引:50
作者
Campo, Laura
Mercadante, Rosa
Rossella, Federica
Fustinoni, Silvia
机构
[1] Univ Milan, Dept Environm & Occupat Hlth, Milan, Italy
[2] Fdn IRCCS Osped Maggiore Policlin, Milan, Italy
关键词
Urinary polycyclic aromatic hydrocarbons; Solid-phase microextraction; Biological monitoring; PERFORMANCE LIQUID-CHROMATOGRAPHY; WASTE-WATER; OCCUPATIONAL-EXPOSURE; 1-HYDROXYPYRENE; EXTRACTION; BIOMARKERS; PAH; METABOLITES; SAMPLES; BLOOD;
D O I
10.1016/j.aca.2008.10.041
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Polycyclic aromatic hydrocarbons (PAHs) are common environmental pollutants in both living and working environments. The aim of this study was the development of a headspace solid-phase microextraction gas chromatography-isotope dilution mass spectrometry (HS-SPME/GC-IDMS) method for the simultaneous quantification of 13 PAHs in urine samples. Different parameters affecting PAHs extraction be HS-SPME were considered and optimized: type/thickness of fiber coatings, extraction temperature/time desorption temperature/time, ionic strength and sample agitation. The stability of spiked PAHs solution and of real urine samples stored up to 90 days in containers of different materials was evaluated. In the optimized method, analytes were absorbed for 60 min at 80 degrees C in the sample headspace with a 100 mu m polydimethylsiloxane fiber. The method is very specific, with linear range from the limit of quantification to 8.67 x 10(3) ng L-1, a within-run precision of <20% and a between-run precision of <20% for 2-, 3- an 4-ring compounds and of <30% for 5-ring compounds, trueness within 20% of the spiked concentration and limit of quantification in the 2.28-2.28 x 10(1) ng L-1 range. An application of the proposed method using 15 urine samples from subjects exposed to PAHs at different environmental levels is shown. (C) 2008 Elsevier B.V. All rights reserve.
引用
收藏
页码:196 / 205
页数:10
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