Ultrasound-assisted emulsification microextraction followed by gas chromatography-mass spectrometry and gas chromatography-tandem mass spectrometry for the analysis of UV filters in water

被引:42
作者
Vila, Marlene [1 ]
Pablo Lamas, J. [1 ]
Garcia-Jares, Carmen [1 ]
Dagnac, Thierry [2 ]
Llompart, Maria [1 ]
机构
[1] Univ Santiago de Compostela, Dept Analyt Chem Nutr & Food Sci, Fac Chem, E-15782 Santiago De Compostela, Spain
[2] Agr & Agron Res Ctr INGACAL CIAM, Unit Organ Contaminants, La Coruna 15080, Spain
关键词
Ultrasound-assisted emulsification microextraction; GC-MS/MS; Personal care products (PCPs); Emerging pollutants; Water samples; UV-filters; LIQUID-LIQUID MICROEXTRACTION; BAR SORPTIVE EXTRACTION; PERSONAL CARE PRODUCTS; ULTRAVIOLET FILTERS; IONIC LIQUID; 4-METHYLBENZYLIDENE CAMPHOR; MULTICLASS DETERMINATION; SENSITIVE DETERMINATION; PHASE MICROEXTRACTION; SAMPLES;
D O I
10.1016/j.microc.2015.09.023
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A methodology based on ultrasound-assisted emulsification microextraction (USAEME) has been developed for the simultaneous analysis of ten UV filters (2-ethylhexyl methoxycinnamate (2EHMC), 4- methylbencylidene camphor (4MBC), benzyl salicylate (BS), ethylhexyl dimethyl PABA (EHPABA), ethylhexyl salicylate (EHS), etocrylene (Eto), homosalate (HMS), isoamyl methoxycinnamate (IAMC), menthyl anthranilate (MA) and octocrylene (OCR)) in different water samples employing two detection modes, gas chromatography-mass spectrometry (GC-MS), and gas chromatography-tandem mass spectrometry (GC-MS/MS). The extraction parameters such as the extraction solvent, the temperature and the time of extraction, and the addition of salt were optimized by means of experimental design tools. Selected conditions were 100 mu L of chloroform, 10 mL of sample, 2 g of salt (NaCl) and 5 min of extraction. Good linearity (R-2>0.9910), quantitative recoveries (>90% for most of compounds) and satisfactory precision (RSD < 10% in most cases) were achieved under the optimal conditions. The methodology was successfully applied to the analysis of different types of water samples including seawater, spas, rivers, swimming pools, and aquaparks, in which most of the target compounds were found at concentrations sometimes over the part per million. Since no significant matrix effect has been found for any of the water types analyzed, quantification could be carried out by using conventional external calibration, thereby allowing a high analytical throughput and a valuable protocol simplification. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:530 / 539
页数:10
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