Determination of nitrofuran residues in avian eggs by liquid chromatography UV photodiode array detection and confirmation by liquid chromatography ionspray mass spectrometry

被引:48
作者
Draisci, R [1 ]
Giannetti, L [1 ]
Lucentini, L [1 ]
Palleschi, L [1 ]
Brambilla, G [1 ]
Serpe, L [1 ]
Gallo, P [1 ]
机构
[1] IST ZOOPROFILATT SPERIMENTALE MEZZOGIORNO,I-80055 PORTICI,NAPOLI,ITALY
关键词
eggs; food analysis; nitrofurans; furazolidone; nitrofurazone; furaltadone;
D O I
10.1016/S0021-9673(97)00247-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A high-performance liquid chromatographic-UV-Vis photodiode-array detection (HPLC-DAD) method for the determination of nitrofuran residues, nitrofurazone, furazolidone and furaltadone, in chicken eggs is described. Confirmation of the identity of nitrofurazone, furazolidone and furaltadone was performed by high-performance liquid chromatography-mass spectrometry (HPLC-MS) using an atmospheric pressure ionization (API) source and an ionspray interface. The nitrofuran residues were extracted from eggs with acetonitrile and the extracts purified by liquid-liquid partitioning. Analytes were chromatographed isocratically with an octadecylsilyl (ODS) column and an UV-Vis detector set at 362 nm and identified by comparing the retention times and W-Vis spectra of the sample peaks with the reference compounds. The HPLC-DAD limit of detection based on a signal-to-noise ratio (S/N) of 3, was estimated to be 2.5 mu g kg(-1) for nitrofurazone and furazolidone and 5.0 mu g kg(-1) for furaltadone. The ionspray HPLC-MS was carried out on the purified extracts. The HPLC-MS method involved the separation of analytes on a C-18 column with acetonitrile-water (50:50, v/v), containing 1 mM ammonium acetate and 0.025% acetic acid, with selected-ion monitoring (SIM) of only protonated molecules, [M+H](+) of the analytes. The overall average recovery in nitrofuran fortified eggs was 85.3+/-3.8% for nitrofurazone, 88.1+/-3.9% for furazolidone and 87.1+/-3.7% for furaltadone. The HPLC-MS limit of detection, based on a S/N of 3, was estimated to be 3.2, 1.6 and 1.0 mu g kg(-1) for nitrofurazone, furazolidone and furaltadone, respectively. HPLC-MS has shown itself to be a sensitive, selective and rapid method and was successfully used for the confirmation analysis of nitrofurazone, furazolidone and furaltadone in avian eggs for regulatory purposes. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:201 / 211
页数:11
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