Development and validation of a stable-isotope dilution liquid chromatography-tandem mass spectrometry method for the determination of bisphenols in ready-made meals

被引:52
|
作者
Regueiro, Jorge [1 ]
Wenzl, Thomas [1 ]
机构
[1] Commiss European Communities, Directorate Gen Joint Res Ctr, Inst Reference Mat & Measurements, B-2440 Geel, Belgium
关键词
Bisphenols; BPA; BPF; BPS; Food; Ready-made meal; SOLID-PHASE EXTRACTION; POLYCHLORINATED-BIPHENYLS; ANALOGS; DERIVATIVES; OPTIMIZATION; ALKYLPHENOLS; QUECHERS;
D O I
10.1016/j.chroma.2015.08.037
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Due to their growing consumption, ready-made meals are a major dietary component for many people in today's society, representing an important potential route of human exposure to several food contaminants. The recent restrictions in the use of bisphenol A have led the plastic industry to look for alternative chemicals, most of them belonging to the same family of p,p'-bisphenols. The aim of the current work was to develop and validate a method based on stable-isotope dilution liquid chromatography-tandem mass spectrometry for the analysis of bisphenol A and its main analogs bisphenol 5, 4,4'-sulfonylbis(2-methylphenol), bisphenol F, bisphenol E, bisphenol B, bisphenol Z, bisphenol AF, bisphenol AP, tetrabromobisphenol A and bisphenol P - in solid foodstuffs, and particularly in ready-made meals. Extraction was carried out by ultrasound-assisted extraction after sample disruption with sand. A selective solid-phase extraction procedure was then applied to reduce potential matrix interferences. Derivatization of bisphenols with pyridine-3-sulfonyl chloride increased their ionization efficiency by electrospray ionization. Validation of the proposed method was performed in terms of selectivity, matrix effects, linearity, precision, measurement uncertainty, trueness and limits of detection. Satisfactory repeatability and intermediate precision were obtained; the related relative standard deviations were <= 7.8% and <= 10%, respectively. The relative expanded uncertainty (k=2) was below 17% for all bisphenol analogs and the trueness of the method was demonstrated by spike recovery experiments. Low limits of detection, in the range from 0.025 mu g kg(-1) to 0.140 mu g kg(-1), were obtained for all compounds. To demonstrate the applicability of the proposed method, it was eventually applied to several ready-made meals purchased from different supermarkets in Belgium. (C) 2015 The Authors. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license
引用
收藏
页码:110 / 121
页数:12
相关论文
共 50 条
  • [11] Determination of cyclophosphamide and ifosfamide in sewage effluent by stable isotope-dilution liquid chromatography-tandem mass spectrometry
    Llewellyn, N.
    Lloyd, P.
    Juergens, M. D.
    Johnson, A. C.
    JOURNAL OF CHROMATOGRAPHY A, 2011, 1218 (47) : 8519 - 8528
  • [12] Stable isotope-dilution liquid chromatography/tandem mass spectrometry method for determination of thyroxine in saliva
    Higashi, Tatsuya
    Ichikawa, Takuya
    Shimizu, Chikara
    Nagai, So
    Inagaki, Shinsuke
    Min, Jun Zhe
    Chiba, Hitoshi
    Ikegawa, Shigeo
    Toyo'oka, Toshimasa
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2011, 879 (13-14): : 1013 - 1017
  • [13] Quantification of key folate forms in serum using stable-isotope dilution ultra performance liquid chromatography-tandem mass spectrometry
    Kirsch, Susanne H.
    Knapp, Jean-Pierre
    Herrmann, Wolfgang
    Obeid, Rima
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2010, 878 (01): : 68 - 75
  • [14] Determination of total phthalates in urine by isotope-dilution-liquid chromatography-tandem mass spectrometry
    Kato, K
    Silva, MJ
    Needham, LL
    Calafat, AM
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2005, 229 : U832 - U832
  • [15] Determination of acrylamide residue in cosmetics by isotope dilution-liquid chromatography-tandem mass spectrometry
    Ma Qiang
    Wang Chao
    Bai Hua
    Wang Xing
    Zhang Qing
    Xiao Haiqing
    Yan Yan
    Dong Yiyang
    Wang Baolin
    CHINESE JOURNAL OF CHROMATOGRAPHY, 2009, 27 (06) : 856 - 859
  • [16] Determination of total phthalates in urine by isotope-dilution liquid chromatography-tandem mass spectrometry
    Kato, K
    Silva, MJ
    Needham, LL
    Calafat, AM
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2005, 814 (02): : 355 - 360
  • [17] Quantitative determination of rifampicin in aquatic products by stable isotope-dilution high liquid chromatography-tandem mass spectrometry
    Li, Qin
    Cao, Jingyuan
    Han, Gang
    Liu, Huan
    Yan, Jie
    Wu, Lidong
    Li, Jincheng
    BIOMEDICAL CHROMATOGRAPHY, 2020, 34 (05)
  • [18] Development and validation of a liquid chromatography-tandem mass spectrometry method for determination of ibuprofen in human plasma
    Puangpetch, Apichaya
    Limrungsikul, Anchalee
    Prommas, Santirhat
    Rukthong, Pattarawit
    Sukasem, Chonlaphat
    CLINICAL MASS SPECTROMETRY, 2020, 15 : 6 - 12
  • [19] A Liquid Chromatography-Tandem Mass Spectrometry Bioanalytical Method Development and Validation for the Determination of Pacritinib in Plasma
    Kumar, Mulamraju Aruna
    Bangaraiah, Pagala
    SEPARATION SCIENCE PLUS, 2024, 7 (12):
  • [20] Development and Validation of a Method for the Determination of Quinolones in Muscle and Eggs by Liquid Chromatography-Tandem Mass Spectrometry
    Loredana Annunziata
    Pierina Visciano
    Arianna Stramenga
    Maria Novella Colagrande
    Guido Campana
    Giampiero Scortichini
    Giacomo Migliorati
    Dario Compagnone
    Food Analytical Methods, 2016, 9 : 2308 - 2320