4.6 Article

Evaluation of magnetic nanoparticles to serve as solid-phase extraction sorbents for the determination of endocrine disruptors in milk samples by gas chromatography mass spectrometry

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1348, Issue -, Pages 71-79

Publisher

ELSEVIER
DOI: 10.1016/j.chroma.2014.04.092

Keywords

Magnetic solid-phase extraction; Magnetite octadecylsilane nanoparticles; Milk; Organochlorine pesticides; Polychlorinated biphenyls; Experimental design

Funding

  1. European Union (European Regional Development Fund-ERDF) [MIS: 348148]
  2. Greek national funds through the Operational Program THESSALY-MAINLAND GREECE AND EPIRUS of National Strategic Reference Framework (NSRF)

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A rapid magnetic solid-phase extraction (MSPE) is proposed based on C18-functionalized magnetic silica nanoparticles as sorbents, for the determination of endocrine disruptors - 20 organochlorine pesticides and 6 polychlorinated biphenyls - in milk samples. Magnetic nanoparticles are characterized by several techniques, such as Scanning Electron Microscopy, X-Ray diffraction, Brunauer-Emmett-Teller and Fourier transform-infrared. The MSPE is performed by dispersion of the Fe3O4@SiO2@C18 nanoparticles in milk samples with sonication, after protein precipitation. Then, the sorbent is collected by applying an external magnetic field and the analytes are desorbed by n-hexane. Several parameters affecting the extraction efficiency of target analytes by the magnetic nanoparticles are investigated, including washing and elution solvents, amount of sorbents, time of extraction and elution, sample and elution solvent volume. The proposed method is optimized by means of experimental design and response surface methodology. When coupled with gas chromatography mass spectrometry detection and under optimum extraction conditions, average recoveries of target analytes are found to be in the range of 79% to 116%. The proposed MSPE GC MS analytical method has a linear calibration curve for all target analytes with coefficients of determination to range from 0.9950 to 0.9999. The limits of quantification are found to be between 0.2 and 1 mu g/L ensuring compliance with the maximum residue limits established by European Commission and Codex Alimentarius, for OCPs and PCBs residues in milk. The proposed method is applied to the determination of target analytes in milk samples from local markets. (C) 2014 Elsevier B.V. All rights reserved.

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