Multiclass Determination of Endocrine-Disrupting Chemicals in Meconium: First Evidence of Perfluoroalkyl Substances in This Biological Compartment

Author:

Domínguez-Liste Aritz1ORCID,de Haro-Romero Teresa23ORCID,Quesada-Jiménez Raquel245ORCID,Pérez-Cantero Ainhoa5,Peinado Francisco Manuel245ORCID,Ballesteros Óscar1ORCID,Vela-Soria Fernando23

Affiliation:

1. Analytical Chemistry and Life Sciences Research Group, Department of Analytical Chemistry, University of Granada, E-18071 Granada, Spain

2. Instituto de Investigación Biosanitaria (ibs.GRANADA), E-18016 Granada, Spain

3. Clinical Laboratory Management Unit, Hospital Universitario Clínico San Cecilio, E-18016 Granada, Spain

4. Centre for Biomedical Research, University of Granada, E-18016 Granada, Spain

5. Radiology and Physical Medicine Department, University of Granada, E-18016 Granada, Spain

Abstract

Major concerns have been raised about human exposure to endocrine-disrupting chemicals (EDCs) during pregnancy. Effective methodologies for the assessment of this exposure are needed to support the implementation of preventive measures and the prediction of negative health effects. Meconium has proven a valuable non-invasive matrix for evaluating cumulative exposure to xenobiotics during the last two trimesters of pregnancy. The study objective was to develop a novel method to determine the presence in meconium of perfluoroalkyl substances (PFASs), bisphenols, parabens, and benzophenones, EDCs that are widely used in the manufacture of numerous consumer goods and personal care products, including cosmetics. Ten PFASs, two bisphenols, four parabens, and four benzophenones were measured in meconium samples prepared by using a combination of Captiva Enhanced Matrix Removal (EMR) lipid cartridges with salt-assisted liquid–liquid extraction (SALLE) and dispersive liquid–liquid microextraction (DLLME) before the application of liquid chromatography–tandem mass spectrometry (LC–MS/MS). Experimental parameters were optimized by applying different chemometric techniques. Limits of detection ranged from 0.05 to 0.1 ng g−1, and between-day variabilities (relative standard deviations) ranged from 6.5% to 14.5%. The method was validated by matrix-matched standard calibration followed by a recovery assay with spiked samples, obtaining percentage recoveries of 89.9% to 114.8%. The method was then employed to measure compounds not previously studied in this matrix in 20 meconium samples. The proposed analytical procedure yields information on cumulative in utero exposure to selected EDCs.

Funder

Miguel Servet Postdoctoral Research

ISCIII

Publisher

MDPI AG

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