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一种用于测定母乳样品中对羟基苯甲酸酯和双酚A的新方法,该方法采用超声辅助萃取,并在超高效液相色谱-串联质谱分析之前用分散吸附剂进行净化处理。

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.

作者信息

Rodríguez-Gómez R, Dorival-García N, Zafra-Gómez A, Camino-Sánchez F J, Ballesteros O, Navalón A

机构信息

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

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

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2015 Jun 15;992:47-55. doi: 10.1016/j.jchromb.2015.04.022. Epub 2015 Apr 20.

Abstract

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 10min. Deuterium-labeled ethylparaben-d5 (EPB-d5) and deuterium-labeled bisphenol A-d16 (BPA-d16) were used as surrogates. The limits of quantification ranged from 0.4 to 0.7ngmL(-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).

摘要

已开发并验证了一种灵敏且准确的分析方法,用于测定人乳样品中的甲基、乙基、丙基和丁基对羟基苯甲酸酯以及双酚A。超声辅助萃取(UAE)与使用吸附剂材料的简化快速净化技术相结合,已成功应用于超高效液相色谱-串联质谱(UHPLC-MS/MS)分析前的样品制备。使用乙腈和超声辐射(在70%振幅下进行三个15分钟循环)从冻干的人乳样品中提取分析物,并进一步用C18吸附剂净化。使用实验设计对影响UAE方法和净化步骤的最具影响力的参数进行了优化。在选择反应监测(SRM)模式下使用负电喷雾电离(ESI)进行质谱检测。每种化合物使用两个反应,可在一次运行中同时进行定量和鉴定。分析物在不到10分钟内分离。使用氘代乙基对羟基苯甲酸酯-d5(EPB-d5)和氘代双酚A-d16(BPA-d16)作为替代物。定量限范围为0.4至0.7 ng mL(-1),而在所有情况下,日内和日间变异性均低于11.1%。在没有认证参考物质的情况下,使用加标样品的回收率测定并采用基质匹配校准来验证该方法。回收率范围为93.8%至112.2%。所提出的方法令人满意地应用于测定从居住在西班牙格拉纳达省的哺乳期母亲获得的人乳样品中的四种选定对羟基苯甲酸酯和双酚A。

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