FOOD SCIENCE ›› 2009, Vol. 30 ›› Issue (4): 178-181.doi: 10.7506/spkx1002-6630-200904036

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Simultaneous Determination of Eight Sulfonamide Residues in Fish Muscle Using Matrix Solid-phase Dispersion Coupled with High Performance Liquid Chromatography Based on Low Toxic Solvent

ZHAO Hai-xiang1,2,3,DENG Wei2,SHANG Yan-fen2,ZHAO Meng-bin2,DING Ming-yu1,*   

  1. (1. Department of Chemistry, Tsinghua University, Beijing 100084, China;2. Enterprise Postdoctoral Workstation, Beijing
    Glorious Land Agricultural Co. Ltd., Zhongguancun (Haidian) Science Park, Beijing 100049, China;3. Department of Basic
    Agricultural Science, Hebei North University, Zhangjiakou 075131, China)
  • Received:2008-03-11 Revised:2008-09-26 Online:2009-02-15 Published:2010-12-29
  • Contact: ZHAO Hai-xiang1,2,3 E-mail:xzhaoh@126.com

Abstract:

A multi-residue analytical method for eight sulfonamides in fish muscle based on matrix solid-phase dispersion (MSPD) coupled with high performance liquid chromatography (HPLC) was developed. This method was environmentally friendly using ethyl acetate as the elution solvent. 0.5 g of fish muscle mixed with 2 g of C18 packing material was grounded and filled into a SPE column. After washing with hexane, sulfonamides were eluted with ethyl acetate and determined using RP-HPLC with UV detector at 270 nm. Sulfonamides were separated on C18 column using 50 mmol/L NaH2PO4-acetonitrile (70:30, V/V) as mobile phase at a flow rate of 0.7 ml/min, and the column temperature was 30 ℃. The linear range of this method is from 0.010 μg/ml to 1.000 μg/ml with the correlation coefficient of over 0.9999. The spike recoveries are in the range of 76.0% to 115.0% and the relative standard deviation (RSD) is less than 6.4% (n = 6). The limit of detection is 0.020 μg/g in a 0.5 g of sample.

Key words: HPLC, fish muscle, MSPD, low toxic solvent, sulfonamide residues

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