Green analytical determination of emerging pollutants in environmental waters using excitation-emission photoinduced fluorescence data and multivariate calibration

被引:21
作者
del Carmen Hurtado-Sanchez, Maria [1 ]
Lozano, Valeria A. [2 ]
Isabel Rodriguez-Caceres, Maria [1 ]
Duran-Meras, Isabel [1 ]
Escandar, Graciela M. [2 ]
机构
[1] Univ Extremadura, Dept Analyt Chem, Badajoz 06006, Spain
[2] Univ Nacl Rosario, Inst Quim Rosario IQUIR CONICET, Fac Ciencias Bioquim & Farmaceut, Dept Quim Analit, RA-2000 Rosario, Argentina
关键词
Emerging pollutants; Photoinduced fluorescence; Unfolded partial least-squares/residual; bilinearization; Water samples; SOLID-PHASE EXTRACTION; PARTIAL LEAST-SQUARES; LINEAR ION-TRAP; WASTE-WATER; SPECTROFLUOROMETRIC METHOD; PHARMACEUTICAL RESIDUES; 2ND-ORDER ADVANTAGE; AQUATIC ENVIRONMENT; MASS-SPECTROMETRY; CONTAMINANTS;
D O I
10.1016/j.talanta.2014.11.022
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An eco-friendly strategy for the simultaneous quantification of three emerging pharmaceutical contaminants is presented. The proposed analytical method, which involves photochemically induced fluorescence matrix data combined with second-order chemometric analysis, was used for the determination of carbamazepine, ofloxacin and piroxicam in water samples of different complexity without the need of chromatographic separation. Excitation-emission photoinduced fluorescence matrices were obtained after UV irradiation, and processed with second-order algorithms. Only one of the tested algorithms was able to overcome the strong spectral overlapping among the studied pollutants and allowed their successful quantitation in very interferent media. The method sensitivity in superficial and underground water samples was enhanced by a simple solid-phase extraction with 08 membranes, which was successful for the extraction/preconcentration of the pollutants at trace levels. Detection limits in preconcentrated (1:125) real water samples ranged from 0.04 to 0.3 ng mL(-1). Relative prediction errors around 10% were achieved. The proposed strategy is significantly simpler and greener than liquid chromatography-mass spectrometry methods, without compromising the analytical quality of the results. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:215 / 223
页数:9
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