Trace analysis of parabens, triclosan and related chlorophenols in water by headspace solid-phase microextraction with in situ derivatization and gas chromatography-tandem mass spectrometry

被引:156
作者
Regueiro, Jorge [1 ]
Becerril, Elias [1 ,2 ]
Garcia-Jares, Carmen [1 ]
Llompart, Maria [1 ]
机构
[1] Univ Santiago de Compostela, Dept Quim Analit Nutr & Bromatol, Inst Invest & Anal Alimentarios, Santiago De Compostela 15782, Spain
[2] Univ Nacl Autonoma Mexico, Inst Ingn, Mexico City 04510, DF, Mexico
关键词
Parabens; Triclosan; Wateranalysis; Solid-phase microextraction; Microextraction; Headspace analysis; Derivatization; Experimental design; PERSONAL-CARE PRODUCTS; P-HYDROXYBENZOIC ACID; FREE-CHLORINE; WASTE-WATER; SAMPLES; EXTRACTION; OPTIMIZATION; PHENOLS; PHARMACEUTICALS; ALKYLPHENOLS;
D O I
10.1016/j.chroma.2009.04.025
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An in situ derivatization sohd-phase microextraction method has been developed for the determination of parabens, triclosan and related chlorophenols in water. Acetylated derivatives are selectively determined using gas chromatography with tandem mass spectrometry. Parameters affecting both derivatization and SPME procedures, such as fiber coating, extraction mode, temperature, volume of derivatizating reagent and ionic strength, are studied and optimized through a multifactorial experimental design. The Quantitative recoveries (>= 82%) and satisfactory precision (RSD <= 12%) are obtained. Limits of detection at the low picogram per millilitre level are achieved for all target Compounds. Linearity is studied in a wide range of concentrations and an analysis of variance with a lack-of-fit test is run to validate the calibration data. Extraction time profiles are also obtained. Finally, the applicability of the proposed method is demonstrated for several real samples including river water, wastewaters and swimming pool water. Since no matrix effects are observed, quantification can readily be carried Out by external calibration with ultrapure water standards. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:4693 / 4702
页数:10
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