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An improved method for simultaneous analysis of steroid and phenolic endocrine disrupting chemicals in biological samples

机译:一种同时分析生物样品中甾体和酚类内分泌干扰物的改进方法

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摘要

An improved method was developed for the simultaneous determination of eight steroid and phenolic endocrine disrupting chemicals, such as oestrone (El), 17β-oestradiol (E2), oestriol (E3), 17α-ethynylestradoil (EE2), 4-nonylphenol (4-NP), bisphenol A (BPA), 4-tert-octylphenol (4-t-OP) and 4-cumylphenol (4-CP), in biological samples. The optimal extraction and clean-up procedures were investigated using microwave-assisted extraction (MAE), automated gel permeation chromatography (GPC) and solid phase extraction (SPE). As a consequence, the most efficient extraction was achieved by using MAE with methanol as solvent at an extraction temperature of 110℃ for 20min. The clean-up of extracts was carried out by GPC on a Biobeads S-X3 column with cyclohexane/ethyl acetate (1:1, v/v) as mobile phase. Target compounds were eluted in the fraction from 7-14 min retention time. Moreover, the cleanest extracts were obtained by solid phase extraction with C-18 cartridges after the elution with 15 mL ethyl acetate. The final sample extracts were derivatised using N,O-bis(trimethylsilyl)trifluoroacetamide (BSTFA) (1% trimethylchlorosilane, TMCS) as derivatisation reagent with pyridine as the solvent. Quantification was performed by gas chromatography-mass spectrometry (GC-MS) with electron ionisation (El) and selected ion monitoring (SIM) mode. The method was validated by spiked samples which showed good recovery and reproducibility. The overall recoveries ranged between 55.1% and 100.6%, with relative standard deviations (RSD) of 2.3-12.7% for the entire procedure. Method detection limits (MDL) ranged from 0.3 to 0.7 ng g~(-1) dry weight (dw). Performance of the method was demonstrated by its application on tissues from fish exposed to high concentration of EDCs in the laboratory. The developed method is a promising approach for the analysis of steroid and phenolic endocrine disrupting chemicals in various biological samples.
机译:开发了一种同时测定八种类固醇和酚类内分泌干扰化学物质的改进方法,例如雌酮(El),17β-雌二醇(E2),雌三醇(E3),17α-乙炔雌二醇(EE2),4-壬基酚(4- NP),双酚A(BPA),4-叔辛基苯酚(4-t-OP)和4-枯基苯酚(4-CP)。使用微波辅助萃取(MAE),自动凝胶渗透色谱(GPC)和固相萃取(SPE)研究了最佳的萃取和净化程序。因此,通过在甲醇中以甲醇为溶剂,在110℃的萃取温度下20分钟,可以实现最有效的萃取。通过GPC在Biobeads S-X3色谱柱上以环己烷/乙酸乙酯(1:1,v / v)作为流动相对提取物进行净化。从7-14分钟保留时间洗脱目标化合物。此外,用15 mL乙酸乙酯洗脱后,使用C-18柱进行固相萃取,可得到最干净的萃取物。最终样品提取物使用N,O-双(三甲基甲硅烷基)三氟乙酰胺(BSTFA)(1%三甲基氯硅烷,TMCS)作为衍生试剂进行衍生化,吡啶为溶剂。通过具有电子电离(E1)和选择的离子监测(SIM)模式的气相色谱-质谱(GC-MS)进行定量。样品加标显示了良好的回收率和重现性,验证了该方法的有效性。总体回收率在55.1%至100.6%之间,整个过程的相对标准偏差(RSD)为2.3-12.7%。方法检测限(MDL)为0.3至0.7 ng g〜(-1)干重(dw)。该方法在实验室中暴露于高浓度EDC的鱼类组织中的应用证明了该方法的有效性。所开发的方法是分析各种生物样品中类固醇和酚类内分泌干扰物的有前途的方法。

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