Determination of Thirteen Nitroimidazole Residues in Fish Blood by Supramolecular Solvent based Dispersive Liquid-Liquid Microextraction/Ultra performance Liquid Chromatography-Tandem Mass Spectrometry
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Determination of Thirteen Nitroimidazole Residues in Fish Blood by Supramolecular Solvent based Dispersive Liquid-Liquid Microextraction/Ultra performance Liquid Chromatography-Tandem Mass Spectrometry
王春, 顾传坤, 马强, 王长海. Determination of Thirteen Nitroimidazole Residues in Fish Blood by Supramolecular Solvent based Dispersive Liquid-Liquid Microextraction/Ultra performance Liquid Chromatography-Tandem Mass Spectrometry[J]. 2019, 38(3): 263-269.
DOI:
王春, 顾传坤, 马强, 王长海. Determination of Thirteen Nitroimidazole Residues in Fish Blood by Supramolecular Solvent based Dispersive Liquid-Liquid Microextraction/Ultra performance Liquid Chromatography-Tandem Mass Spectrometry[J]. 2019, 38(3): 263-269.DOI: doi:10.3969/j.issn.1004-4957.2019.03.001.
Determination of Thirteen Nitroimidazole Residues in Fish Blood by Supramolecular Solvent based Dispersive Liquid-Liquid Microextraction/Ultra performance Liquid Chromatography-Tandem Mass Spectrometry
A novel method was developed for the determination of thirteen nitroimidazoles in fish blood by ultra performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS) with supramolecular solvent based dispersive liquid-liquid microextraction.The target compounds in fish blood were extracted with a supramolecular solvent consisted of octanol
tetrahydrofuran and water.The analytes were separated on a Waters ACQUITY UPLC BEH C18 column(2.1 mm×50 mm×1.7 μm) by gradient elution with acetonitrile-water as mobile phases.The qualitative and quantitative analyses were conducted by electrospray ionization mass spectrometry in positive ion mode under multiple reaction monitoring(MRM) mode.Experimental results demonstrated that good linearities for the analytes were observed in their respective concentration ranges with correlation coefficients(r2) larger than 0.998.The limits of detection(LOD) and the limits of quantitation(LOQ) were in the ranges of 0.05-0.2 μg/L and 0.1-0.5 μg/L
respectively.Recoveries for 13 nitroimidazoles at three spiked levels ranged from 88.4% to 105% with relative standard deviations(n=6) of 4.3%-11%.The method was simple
rapid
accurate and reliable
and could be used for the analysis of nitroimidazole residues in fish blood samples.
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引言
Definition Clarification and Detection Reliability Analysis of Environmental Micro/Nanoplastics
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