首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Quantification of of emerging micropollutants in an amphipod crustacean by nanoliquid chromatography coupled to mass spectrometry using multiple reaction monitoring cubed mode
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Quantification of of emerging micropollutants in an amphipod crustacean by nanoliquid chromatography coupled to mass spectrometry using multiple reaction monitoring cubed mode

机译:纳米液相色谱-质谱联用多反应监测立方模式的质谱联用定量分析两栖类甲壳动物中新兴的微污染物

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An innovative analytical method has been developed to quantify the bioaccumulation in an amphipod crustacean (Gammarus fossarum) of three micropollutants regarded as anthropic-pollution markers: carbamazepine, oxazepam, and testosterone. A liquid-liquid extraction assisted by salts, known as QuEChERS (Quick, Easy, Cheap, Effective, Rugged, and Safe) was miniaturised and optimised, so it could be adapted to the low mass samples (approximatively 5 mg dry weight). For this same reason and in order to obtain good sensitivity, ultra-trace analyses were carried out by means of nanoliquid chromatography. A pre-concentration system by on-column trapping was optimised to increase the injection volume. In order to improve both sensitivity and selectivity, the multiple reaction monitoring cubed mode analyses (MRM3) were carried out, validated and compared to the classic MRM. To the best of our knowledge, this is the first time that MRM3 is coupled to nanoliquid chromatography for the analysis and detection of organic micropollutants <300 Da. The optimised extraction method exhibited recoveries superior to 80%. The limits of quantification of the target compounds were 0.3, 0.7 and 4.7 ng/g (wet weight) for oxazepam, carbamazepine and testosterone, respectively and the limits of detection were 0.1, 0.3 and 2.2 ng/g (wet weight), respectively. The intra- and inter-day precisions were inferior to 7.7% and 10.9%, respectively, for the three levels of concentration tested. The analytical strategy developed allowed to obtain limits of quantification lower than 1 ng/g (wet weight) and to establish the kinetic bioconcentration of contaminants within G. fossarum. (C) 2016 Elsevier B.V. All rights reserved.
机译:已经开发出一种创新的分析方法来定量在两栖类甲壳动物(Gammarus fossarum)中被认为是人类污染标志物的三种微污染物:卡马西平,奥沙西m和睾丸激素的生物富集。借助QuEChERS(快速,简便,便宜,有效,坚固耐用和安全)的盐辅助液-液萃取方法,已进行了小型化和优化,因此可适用于低质量样品(干重约5 mg)。由于相同的原因,并且为了获得良好的灵敏度,借助于纳米液相色谱法进行了超痕量分析。通过柱上捕集对预浓缩系统进行了优化,以增加进样量。为了提高灵敏度和选择性,进行了多反应监测立方模式分析(MRM3),并与经典MRM进行了比较。据我们所知,这是MRM3首次与纳米液相色谱结合用于分析和检测<300 Da的有机微量污染物。优化的提取方法显示出超过80%的回收率。奥沙西m,卡马西平和睾丸激素的目标化合物的定量限分别为0.3、0.7和4.7 ng / g(湿重),检出限分别为0.1、0.3和2.2 ng / g(湿重)。对于三个浓​​度测试水平,日内和日间精度分别低于7.7%和10.9%。制定的分析策略允许获得低于1 ng / g(湿重)的定量极限,并建立了镰刀菌内污染物的动态生物浓度。 (C)2016 Elsevier B.V.保留所有权利。

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