4.6 Article

A novel extraction method for simultaneous determination of neonicotinoid insecticides and their metabolites in human urine

期刊

ANALYTICAL METHODS
卷 11, 期 19, 页码 2571-2578

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9ay00288j

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资金

  1. Natural Science Foundation of China [21677184, 41303094]
  2. Pearl River S&T Nova Program of Guangzhou
  3. Natural Science Foundation of Guangdong Province, China [2015A030313869]
  4. Shenzhen Government Research Projects [JCYJ20160428143348745]
  5. Guangzhou Key Laboratory of Environmental Exposure and Health [GZKLEEH201606]
  6. State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences [KF2016-25]

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In this study, a novel method (i.e., liquid-liquid micro-extraction, LLME) coupled to liquid chromatography tandem mass spectrometry is proposed for the simultaneous determination of urinary levels of six neonicotinoid insecticides (NEOs), namely, imidacloprid, clothianidin, acetamiprid, thiacloprid, thiamethoxam, and dinotefuran, and four metabolites, including 1-methyl-3-(tetrahydro-3-furylmethyl) guanidine, 1-methyl-3-(tetrahydro-3-furylmethyl) urea, 5-hydroxy-imidacloprid, and N-demethyl-acetamiprid has been developed. Ethyl acetate was used as the extraction solvent, and the supernatant was concentrated and dissolved by methanol. The method was validated for repeatability, reproducibility, linearity, and percent recovery. Satisfactory recovery of the NEOs and their metabolites (71-107%) was observed with intraday relative standard deviations (RSDs, n = 3) of 2-11% and inter-day RSDs (n = 9) of 3-17%. Good linearity (R-2 > 0.99) was obtained for all analytes. Limits of quantification and detection for all target analytes ranged from 0.01 ng mL(-1) to 0.1 ng mL(-1) and from 0.003 ng mL(-1) to 0.03 ng mL(-1), respectively. Trace levels of NEOs and their metabolites were found in human urine samples (mean: 0.06-1.99 ng mL(-1)). To the best of our knowledge, this study is the first to apply the proposed LLME method for simultaneous identification and quantification of NEOs and their metabolites in urine samples.

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