4.6 Article

Simultaneous determination of a variety of endocrine disrupting compounds in carrot, lettuce and amended soil by means of focused ultrasonic solid-liquid extraction and dispersive solid-phase extraction as simplified clean-up strategy

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1389, Issue -, Pages 8-18

Publisher

ELSEVIER
DOI: 10.1016/j.chroma.2015.02.036

Keywords

Endocrine-disrupting compound; Vegetables Compost amended soil; Focused ultrasonic solid-liquid extraction; Dispersive solid-phase extraction; Liquid chromatography-tandem mass spectrometry

Funding

  1. Ministerio de Ciencia e Innovacion (MICINN) [CTM2011-24094]
  2. Basque Government
  3. Fundacion Iberdrola

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The present study is focused on the development of an analytical method based on focused ultrasonic solid-liquid extraction (FUSLE) followed by dispersive solid-phase extraction (dSPE) clean-up and liquid chromatography-triple quadrupole tandem mass spectrometry (LC-MS/MS) optimised for the simultaneous analysis of certain endocrine disrupting compounds (EDCs), including alkylphenols (APs), bisphenol A (BPA), triclosan (TCS) and several hormones and sterols in vegetables (lettuce and carrot) and amended soil samples. Different variables affecting the chromatographic separation, the electrospray ionisation and mass spectrometric detection were optimised in order to improve the sensitivity of the separation and detection steps. Under the optimised extraction conditions (sonication of 5 min at 33% of power with pulse times on of 0.8 s and pulse times off of 0.2 s in 10 mL of n-hexane:acetone (30:70, v:v) mixture using an ice bath), different dSPE clean-up sorbents, such as Florisil, Envi-Carb, primary-secondary amine bonded silica (PSA) and C-18, or combinations of them were evaluated for FUSLE extracts before LC-MS/MS. Apparent recoveries and precision in terms of relative standard deviation (RSDs %) of the method were determined at two different fortification levels (according to the matrix and the analyte) and values in the 70-130% and 2-27% ranges, respectively, were obtained for most of the target analytes and matrices. Matrix-matched calibration approach and the use of labelled standards as surrogates were needed for the properly quantification of most analytes and matrices. Method detection limits (MDLs), estimated with fortified samples, in the ranges of 0.1-100 ng/g for carrot, 0.2-152 ng/g for lettuce and 0.9-31 ng/g for amended soil were obtained. The developed methodology was applied to the analysis of 11 EDCs in both real vegetable bought in a local market and in compost (from a local wastewater treatment plant, WWTP) amended soil samples. (C) 2015 Elsevier B.V. All rights reserved.

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