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首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Matrix solid phase dispersion for the extraction of selected endocrine disrupting chemicals from human placental tissue prior to UHPLC-MS/MS analysis
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Matrix solid phase dispersion for the extraction of selected endocrine disrupting chemicals from human placental tissue prior to UHPLC-MS/MS analysis

机译:基质固相分散体,用于在进行UHPLC-MS / MS分析之前从人胎盘组织中提取选定的内分泌干扰化学物质

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摘要

In recent decades, in parallel to industrial development, a large amount of new chemicals have emerged that are able to produce disorders in the human endocrine system. These groups of substances, so-called endocrine disrupting chemicals (EDCs), include many families of compounds, such as parabens, benzophenones and bisphenols. Given the demonstrated biological activity of those compounds, it is necessary to develop new analytical procedures to evaluate the exposure with the final objective of establishing, in an accurate way, relationships between EDC concentrations and the harmful health effects observed in the population. In the present study, a method based on a sample treatment by matrix solid phase dispersion (MSPD) for the extraction of four parabens (methyl-, ethyl-, propyl- and butylparaben), five bisphenols (bisphenol A and monochloro-, dichloro-, trichloro- and tetrachlorobisphenol A) and benzophenone-3 in human placental tissue samples, followed by ultra high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) analysis is proposed. The extraction parameters were accurately optimized using multivariate optimization strategies. Ethylparaben ring-C-13(6), benzophenone-d(10) and bisphenol A-d(16) were used as surrogates. The found limits of quantification (LOQ) ranged from 0.2 to 0.4 ng g(-1) and the precision, evaluated as relative standard deviation, ranged from 6.1% to 14.8%. The method was validated using matrix-matched standard calibration followed by a recovery assay with spiked samples. Recovery rates from 96% to 105% were obtained. The method was satisfactorily applied for the determination of target compounds in human placenta samples from 10 randomly selected women. (C) 2014 Elsevier B.V. All rights reserved.
机译:近几十年来,与工业发展并行的是,出现了能够在人类内分泌系统中引起疾病​​的大量新化学物质。这些物质组,即所谓的内分泌干扰化学物质(EDC),包括许多家族的化合物,例如对羟基苯甲酸酯,二苯甲酮和双酚。鉴于这些化合物具有证明的生物活性,有必要开发新的分析程序来评估暴露,最终目标是准确确定EDC浓度与人群中观察到的有害健康影响之间的关系。在本研究中,一种基于样品固相分散体(MSPD)处理的方法,用于萃取四种对羟基苯甲酸酯(甲基,乙基,丙基和丁基对羟基苯甲酸酯),五种双酚(双酚A和一氯-,二氯- ,建议在人胎盘组织样品中使用三氯和四氯双酚A)和二苯甲酮3,然后提出超高效液相色谱-串联质谱(UHPLC-MS / MS)分析。使用多元优化策略可以精确地优化提取参数。对羟基苯甲酸乙酯环-C-13(6),二苯甲酮-d(10​​)和双酚A-d(16)用作替代物。发现的定量限(LOQ)为0.2至0.4 ng g(-1),以相对标准偏差评估的精度为6.1%至14.8%。该方法通过与基质匹配的标准校准物进行了验证,然后使用加标样品进行了回收率测定。获得了96%至105%的回收率。该方法令人满意地用于测定10名随机选择的妇女的人胎盘样品中的目标化合物。 (C)2014 Elsevier B.V.保留所有权利。

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