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Determination of Four Nitrofurans in Water and Sediment Using Ultra Performance Liquid Chromatography

WANG Qiang, WANG Xufeng, ZHAO Donghao, HUANG Ke, LI Zhiguang, LI Yongxian, YANG Hongliang, LI Liudong   

  1. South China Sea Fisheries Research Institute, Key Laboratory of Aquatic Product Processing, Ministry of Agriculture,
    Laboratory of Quality and Safety Risky Assessment for Aquatic Product on Storage and Preservation, Ministry of Agriculture,
    Chinese Academy of Fishery Sciences, Guangzhou 510300, China
  • Online:2016-08-25 Published:2016-08-30
  • Contact: LI Liudong

Abstract:

An ultra performance liquid chromatography (UPLC) method was developed for the simultaneous determination
of 4 nitrofuran antibiotics (furazolidone, furaltadone, nitrofurazone and nitrofurantion) in water and sediment. Water
samples were filtrated and cleaned up using mixed-mode cation exchange solid-phase extraction column (MCX). Sediment
samples were extracted with acetonitrile-0.1% formic acid solution (8:2, V/V), and then cleaned up also with MCX solidphase
extraction column. The analytes were separated on a BEH C18 column (100 mm × 2.1 mm, 1.7 μm) utilizing gradient
elution with a mixture of acetonitrile and 0.1% formic acid solution as the mobile phase. The method showed good linearity
in the range of 10.0–200 μg/L with correlation coefficients (R2) all above 0.999. The recoveries were 81.5%–103.2% and
73.3%–91.9% with relative standard deviations (RSDs, n = 5) of 2.0%–5.8% and 3.4%–9.6% for 4 nitrofurans in water and
sediment, respectively. The limits of detection (LODs) were 0.03 μg/L and 0.6 μg/kg and the limits of quantitation (LOQ)
were 0.1 μg/L and 2.0 μg/kg, respectively. The method can be applied to the determination of nitrofuran antibiotics residues
in water and sediment.

Key words: ultra performance liquid chromatography (UPLC), water, sediment, nitrofuran

CLC Number: