液相色谱-串联质谱同时测定血清、尿液和卵泡液中邻苯二甲酸酯和双酚a的方法的建立和验证

IF 2.1 Q4 Chemistry
Anna Pia Dima , Lucia De Santis , Cristina Verlengia , Francesco Lombardo , Andrea Lenzi , Monica Mazzarino , Francesco Botrè , Donatella Paoli , on behalf of the Italian Society of Embryology, Reproduction, Research (SIERR)
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引用次数: 10

摘要

邻苯二甲酸酯和双酚A干扰内源性激素的合成、分泌、运输、结合、代谢和排泄,因此被归类为内分泌干扰物。我们在这里提出了一种同时检测不同生物液体(尿液、血清和滤泡液)中六种邻苯二甲酸盐代谢物和双酚A的分析方法,该方法采用液相色谱-串联质谱联用技术。定量是在负电喷雾电离模式下进行的,选择反应监测作为采集模式。比较评价了固相萃取和液/液萃取两种不同的提取方法,以优化样品制备工艺。选择固相萃取法,以保证最佳的回收率和总灵敏度。该方法经验证,回收率在71±2% ~ 107±6%范围内变化,取决于所考虑的目标分析物和基质,卵泡液的测定内和测定间精度≤12%,血清≤11%,尿液≤10%,卵泡液的测定内和测定间精度≤115%,血清≤113%≤115%,尿液≤115%,线性R2 >0.99,除MEP外(卵泡液回收率64±8%,测定内精密度≤20%,测定间精密度≤16%)。本研究开发并验证的方法的实际适用性,通过分析实际样品,包括10份卵泡液、血清和尿液样本,显示邻苯二甲酸酯代谢物和双酚A的存在,并确认新开发的方法可以应用于常规临床实验室对这些内分泌干扰物质进行鉴定和定量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development and validation of a liquid chromatography-tandem mass spectrometry method for the simultaneous determination of phthalates and bisphenol a in serum, urine and follicular fluid

Phthalates and bisphenol A interfere with the synthesis, secretion, transport, binding, metabolism, and excretion of endogenous hormones and, for this reason, are classified as endocrine disruptors.

We are here presenting an analytical method for the simultaneous detection of six phthalates metabolites and bisphenol A in different biological fluids (urine, serum and follifular fluid) by liquid chromatography coupled to tandem mass spectrometry. The quantification was carried out in negative electrospray ionization mode using selected reaction monitoring as acquisition mode. Different extraction protocols, using either solid phase or liquid/liquid extraction, were comparatively evaluated to optimize the sample preparation procedure. Solid-phase extraction was chosen as it ensured the best recovery and overall sensitivity. The method was successfully validated: recovery varying in the range 71 ± 2%–107 ± 6% depending on the target analyte and the matrix considered, intra-assay and inter-assay precision ≤ 12% for follicular fluid, ≤11% for serum and ≤ 10% for urine and accuracy ≤ 115% for follicular fluid, ≤113% for serum ≤ 115% for urine , linearity with R2 > 0.99, with the exception of MEP (recovery 64 ± 8%, intra-assay precision ≤ 20%, inter-assay precision ≤ 16% for follicular fluid). The actual applicability of the method developed and validated in this study was assessed by the analysis of real samples, including 10 specimens of follicular fluid, serum and urine samples, that showed the presence of phthalates metabolites and Bisphenol A, and confirming that the newly developed method can be applied in the routine clinical laboratory for the identification and quantitation of these endocrine-disrupting chemicals.

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来源期刊
Clinical Mass Spectrometry
Clinical Mass Spectrometry Chemistry-Spectroscopy
CiteScore
1.70
自引率
0.00%
发文量
0
期刊介绍: Clinical Mass Spectrometry publishes peer-reviewed articles addressing the application of mass spectrometric technologies in Laboratory Medicine and Clinical Pathology with the focus on diagnostic applications. It is the first journal dedicated specifically to the application of mass spectrometry and related techniques in the context of diagnostic procedures in medicine. The journal has an interdisciplinary approach aiming to link clinical, biochemical and technological issues and results.
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