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首页> 外文期刊>Microchemical Journal: Devoted to the Application of Microtechniques in all Branches of Science >Approach based on multiple monolithic fiber solid-phase microextraction coupled to liquid chromatography-tandem mass spectrometry for sensitive determination of perfluoroalkyl acids in fish and seafood
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Approach based on multiple monolithic fiber solid-phase microextraction coupled to liquid chromatography-tandem mass spectrometry for sensitive determination of perfluoroalkyl acids in fish and seafood

机译:基于多重整体纤维固相微萃取的方法,耦合到液相色谱 - 串联质谱法,用于敏感鱼类和海鲜全氟烷基酸的敏感测定

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摘要

A sensitive analytical approach using liquid chromatography-tandem mass spectrometry (LC-MS/MS) with multiple monolithic fiber solid-phase microextraction (MMF-SPME) was developed for determination of perfluoroalkyl acids, including perfluorocarboxylic acids (PFCAs) and perfluorosulfonic acids (PFSAs) in fish and seafood. The MMF-SPME based on poly (vinylbenzyltrimethylammonium chloride/dodecafluoroheptyl acrylateco- ethylenedimethacrylate/divinylbenzene) monolith which contained abundant F atoms and quaternary amine groups was employed to effectively extract studied analytes. Various parameters affecting the extraction performance were investigated in detail. Under the most favorable conditions, the developed method displayed wide linear dynamic ranges with good coefficients of correlation (R-2 > 0.99). The limits of detection (LODs) and limits of quantification (LOQs) were in the ranges of 0.0062-1.5 mu g/kg and 0.021-5.0 mu g/kg, respectively. The relative standard deviation (RSD) values for infra-day and inter-day assay variability were less than 12% for all analytes. The introduced method was successfully applied to detect low levels of PFCAs and PFSAs in the muscle of fish, shrimp and shellfish samples. Recoveries at low, medium and high fortified concentrations were in the ranges of 80.2-119%, and the RSDs varied from 0.3% to 11% for all analytes. The satisfactory results well demonstrate that the developed approach is sensitive and reliable in the monitoring of trace PFCAs and PFSAs in fish and seafood.
机译:利用具有多种单片纤维固相微萃取(MMF-SPME)的液相色谱 - 串联质谱(LC-MS / MS)的敏感性分析方法用于测定全氟烷基酸,包括全氟羧酸(PFCAS)和全氟磺酸(PFSAS) )在鱼和海鲜。采用基于聚(乙烯基苄基三甲基氯化铵/十二烷氟庚烷丙烯酰基二甲基二甲基二甲基丙烯酸酯/二乙烯基苯)的MMF-SPME,其含有丰富的F原子和季胺基团,有效提取研究分析物。详细研究了影响提取性能的各种参数。在最有利的条件下,开发方法显示了具有良好相关系数的宽线性动态范围(R-2> 0.99)。检测限(LOD)和定量限制(LOQ)分别为0.0062-1.5μg/ kg和0.021-5.0μg/ kg的范围。所有分析物的Infra-Day和白天测定变异性的相对标准偏差(RSD)值小于12%。介绍的方法已成功应用于检测鱼,虾和贝类样品肌肉中的低水平的PFCA和PFSA。低,中和高强化浓度的回收率在80.2-119%的范围内,所有分析物的RSDS可从0.3%变化至11%。令人满意的结果良好证明,在鱼类和海鲜的痕量PFCA和PFSA的监测中,发达的方法是敏感的并且可靠。

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