New method for the determination of parabens and bisphenol A in human milk samples using ultrasound-assisted extraction and clean-up with dispersive sorbents prior to UHPLC-MS/MS analysis

被引:37
|
作者
Rodriguez-Gomez, R. [1 ]
Dorival-Garcia, N. [1 ]
Zafra-Gomez, A. [1 ]
Camino-Sanchez, F. J. [1 ]
Ballesteros, O. [1 ]
Navalon, A. [1 ]
机构
[1] Univ Granada, Dept Analyt Chem, Res Grp Analyt Chem & Life Sci, E-18071 Granada, Spain
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2015年 / 992卷
关键词
Human milk; Endocrine disrupting chemicals; Ultrasound-assisted extraction; Sorbent materials; UHPLC-MS/MS; HUMAN BREAST-MILK; SOLID-PHASE EXTRACTION; CHLORINATED DERIVATIVES; HUMAN EXPOSURE; ENVIRONMENTAL PHENOLS; GAS-CHROMATOGRAPHY; SEWAGE-SLUDGE; CHEMICALS; MICROEXTRACTION; TOXICITY;
D O I
10.1016/j.jchromb.2015.04.022
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A sensitive and accurate analytical method for the determination of methyl-, ethyl-, propyl- and butylparaben and bisphenol A in human milk samples has been developed and validated. The combination of ultrasound-assisted extraction (UAE) and a simplified and rapid clean-up technique that uses sorbent materials has been successfully applied for the preparation of samples prior to ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) analysis. The analytes were extracted from freeze-dried human milk samples using acetonitrile and ultrasonic radiation (three 15-min cycles at 70% amplitude), and further cleaned-up with C18 sorbents. The most influential parameters affecting the UAE method and the clean-up steps were optimized using design of experiments. Negative electrospray ionization (ESI) in the selected reaction monitoring (SRM) mode was used for MS detection. The use of two reactions for each compound allowed simultaneous quantification and identification in one run. The analytes were separated in less than 10 min. Deuterium-labeled ethylparaben-d(5) (EPB-d(5)) and deuterium-labeled bisphenol A-d(16) (BPA-d(16)) were used as surrogates. The limits of quantification ranged from 0.4 to 0.7 ng mL(-1), while inter- and intra-day variability was under 11.1% in all cases. In the absence of certified reference materials, recovery assays with spiked samples using matrix-matched calibration were used to validate the method. Recovery rates ranged from 93.8% to 112.2%. The proposed method was satisfactorily applied for the determination of four selected parabens and bisphenol A in human milk samples obtained from nursing mothers living in the province of Granada (Spain). (C) 2015 Elsevier B.V. All rights reserved,
引用
收藏
页码:47 / 55
页数:9
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