A novel headspace solid-phase microextraction method using in situ derivatization and a diethoxydiphenylsilane fibre for the gas chromatography-mass spectrometry determination of urinary hydroxy polycyclic aromatic hydrocarbons

被引:28
|
作者
Mattarozzi, M. [1 ]
Musci, M. [1 ]
Careri, M. [1 ]
Mangia, A. [1 ]
Fustinoni, S. [2 ,3 ]
Campo, L. [2 ,3 ]
Bianchi, F. [1 ]
机构
[1] Univ Parma, Dipartimento Chim Gen & Inorgan, I-43100 Parma, Italy
[2] Univ Milan, Dipartimento Med Lavoro & Ambientale, I-20122 Milan, Italy
[3] Fdn Osped Policlin, I-20122 Milan, Italy
关键词
Solid-phase microextraction; Hydroxy polycyclic aromatic hydrocarbons; Urine; Derivatization; Experimental design; EXTRACTION-THERMAL DESORPTION; MONOHYDROXY METABOLITES; OCCUPATIONAL-EXPOSURE; 1-HYDROXYPYRENE; PHENANTHRENE; PYRENE; PAH; OPTIMIZATION; NAPHTHALENE; VALIDATION;
D O I
10.1016/j.chroma.2009.05.072
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An innovative and simple headspace solid-phase microextraction method using a novel diethoxy-diphenylsilane fibre based on in situ derivatization with acetic anhydride was optimized and validated for the gas chromatography-mass spectrometry determination of some monohydroxy metabolites of polycyclic aromatic hydrocarbons, namely 1 -hydroxynaphthalene, 2-hydroxynaphtalene, 9-hydroxyfluorene, 2-hydroxyfluorene and 1-hydroxypyrene at trace levels in human urine. Enzymatic hydrolysis was applied before derivatization, whereas extraction conditions, i.e. the effects of time and temperature of extraction and salt addition were investigated by experimental design. Regression models and desirability functions were applied to find the experimental conditions providing the highest global extraction response. These conditions were found in correspondence of an extraction temperature of 90 degrees C, an extraction time of 90 min and 25% NaCl added to urine samples. The capabilities of the developed method were proved obtaining limit of quantitations in the 0.1-2 mu g/l range, thus allowing the bio-monitoring of these compounds in human urine. A good precision was observed both in terms of intra-batch and inter-batch repeatability with RSD always lower than 14%. Recoveries ranging from 98(+/- 3) to 121(+/- 1)% and extraction yields higher than 72% were also obtained. Finally, the analysis of urine specimens of coke-oven workers revealed analytes' concentrations in the 2.2-164 mu g/l range, proving the exposure to PAHs of the involved workers. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:5634 / 5639
页数:6
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