Detection of chloramphenicol and chloramphenicol glucuronide residues in poultry muscle, honey, prawn and milk using a surface plasmon resonance biosensor and Qflex® kit chloramphenicol

被引:113
作者
Ferguson, J
Baxter, A
Young, P
Kennedy, G
Elliott, C
Weigel, S
Gatermann, R
Ashwind, H
Stead, S
Sharman, M
机构
[1] XenoSense Ltd, Innovat Ctr, Belfast BT3 9DT, Antrim, North Ireland
[2] Dept Agr & Rural Dev, Vet Sci Div, Belfast BT4 3SD, Antrim, North Ireland
[3] Eurofins Wiertz Eggert Jorissen, D-21107 Hamburg, Germany
[4] Dept Environm Food & Rural Affairs, Cent Sci Lab, York YO41 1LZ, N Yorkshire, England
关键词
chloramphenicol; chloramphenicol glucuronide; residue; surface plasmon resonance;
D O I
10.1016/j.aca.2004.11.042
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Immunochemical screening assays using surface plasmon resonance have been developed for chloramphenicol and chloramphenicol glucuronide residues in poultry muscle, honey, prawn and cows' milk using a sensor chip coated with a chloramphenicol derivative and an antibody. The antibody cross-reacted with chloramphenicol glucuronide 73.8% (poultry), 69.2% (honey), 75.7% (prawn) and 84.8% (milk). There was no cross-reaction with similar drugs or other commonly used antibiotics. The assay allowed the direct analysis of bovine milk (fat content similar to3.5%). Poultry, honey and prawn samples were extracted with ethyl acetate followed by analysis on the biosensor. The decision limits (Me) for each assay were determined as: poultry (0.005 mug kg(-1)), honey (0.02 mug kg(-1)), prawn (0.04 mug kg(-1)) and milk (0.04 mug kg(-1)) and the detection capabilities (CCbeta) were 0.02, 0.02, 0.07 and 0.05 mug kg(-1), respectively. Poultry muscle, honey and milk were spiked at 0.1 mug kg(-1) and prawn at 0.15 mug kg(-1) and the intra-assay precision (n = 10) calculated as 10.5, 5.0, 4.6 and 8.8%, respectively. Between run precision (n = 3) performed at the same levels yielded the following results: 3.0% (poultry), 4.7% (honey), 7.6% (milk) and 5.5% (prawn). (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:109 / 113
页数:5
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