Reliable quantification of bisphenol A and its chlorinated derivatives in human urine using UPLC–MS/MS method

Bisphenol A (BPA), a widespread man-made chemical classified as an endocrine disruptor, is increasingly considered as a major cause of concern for human health. Chlorine present in drinking water may react with BPA to form chlorinated derivatives (ClxBPA), which have demonstrated a heightened level...

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Veröffentlicht in:Talanta (Oxford) 2014-07, Vol.125, p.284-292
Hauptverfasser: Venisse, N., Grignon, C., Brunet, B., Thévenot, S., Bacle, A., Migeot, V., Dupuis, A.
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container_start_page 284
container_title Talanta (Oxford)
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creator Venisse, N.
Grignon, C.
Brunet, B.
Thévenot, S.
Bacle, A.
Migeot, V.
Dupuis, A.
description Bisphenol A (BPA), a widespread man-made chemical classified as an endocrine disruptor, is increasingly considered as a major cause of concern for human health. Chlorine present in drinking water may react with BPA to form chlorinated derivatives (ClxBPA), which have demonstrated a heightened level of estrogenic activity. If many epidemiological studies report that more than 90% of people have detectable BPA levels in their urine, then no such study has been undertaken regarding ClxBPA. The purpose of this work is to propose a highly sensitive and accurate analytical method adapted to large-scale biomonitoring studies aimed at assessing exposure to BPA and ClxBPA through the use of human urine. To achieve this, we have comprehensively validated a method using salting-out assisted liquid/liquid extraction (SALLE) coupled to UPLC–MS/MS and isotope dilution quantification, to measure unconjugated BPA and ClxBPA in human urine according to the accepted guidelines. Deutered BPA as well as deutered 2,2′-DCBPA was used as internal standards. The matrix calibration curve ranged from 0.05 to 1.60ngmL−1 and from 0.5 to 16.0ngmL−1 for ClxBPA and BPA respectively, and provided good linearity (r²>0.99). This method was precise (the intra- and inter-day coefficients of variation were
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Chlorine present in drinking water may react with BPA to form chlorinated derivatives (ClxBPA), which have demonstrated a heightened level of estrogenic activity. If many epidemiological studies report that more than 90% of people have detectable BPA levels in their urine, then no such study has been undertaken regarding ClxBPA. The purpose of this work is to propose a highly sensitive and accurate analytical method adapted to large-scale biomonitoring studies aimed at assessing exposure to BPA and ClxBPA through the use of human urine. To achieve this, we have comprehensively validated a method using salting-out assisted liquid/liquid extraction (SALLE) coupled to UPLC–MS/MS and isotope dilution quantification, to measure unconjugated BPA and ClxBPA in human urine according to the accepted guidelines. Deutered BPA as well as deutered 2,2′-DCBPA was used as internal standards. 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The matrix calibration curve ranged from 0.05 to 1.60ngmL−1 and from 0.5 to 16.0ngmL−1 for ClxBPA and BPA respectively, and provided good linearity (r²&gt;0.99). This method was precise (the intra- and inter-day coefficients of variation were &lt;20% at three different concentrations: 0.05ngmL−1, 0.2ngmL−1, 0.8ngmL−1 and 0.5ngmL−1, 2ngmL−1, 8ngmL−1 for ClxBPA and BPA, respectively) and accurate (bias ranged from −13% to +12%). The limit of quantification, validated at 0.05ngmL−1 and 0.5ngmL−1 for ClxBPA and BPA respectively when using 300µL of urine, was found to be suitable for the concentration existing in real samples. The matrix effect and the BPA cross-contamination were also investigated in this study. The analytical method developed in this study is in accordance with the requirements applicable to biomonitoring of BPA and ClxBPA in human urine. BPA and ClxBPA were found in human urine samples using UPLC–MS/MS with SALLE. [Display omitted] •An UPLC–MS/MS assay was developed for BPA and ClxBPA in urine in the pg/mL range.•Sample preparation used a simple salting-out liquid–liquid extraction (SALLE).•SIL-IS (BPA-d16 and DCBPA-d12) were used for quantification.•Assay was validated using standards and QCs prepared in human urine.•Sensitivity of the assay allows the determination of target analytes in human urine.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>24840445</pmid><doi>10.1016/j.talanta.2014.02.064</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-3713-219X</orcidid><orcidid>https://orcid.org/0000-0002-7466-6388</orcidid></addata></record>
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subjects Benzhydryl Compounds - urine
Bisphenol A
Bisphenol A chlorinated derivatives
Calibration
Catalysis
Chemical Sciences
Chemistry Techniques, Analytical
Chlorination
Chlorine - analysis
Chromatography, High Pressure Liquid
Derivatives
Human
Humans
LC–MS/MS
Linearity
Liquids
Mathematical analysis
Phenols - urine
Reproducibility of Results
Sensitivity and Specificity
Tandem Mass Spectrometry
Urinalysis - standards
Urine
Urine - chemistry
title Reliable quantification of bisphenol A and its chlorinated derivatives in human urine using UPLC–MS/MS method
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