Multiclass and multi-residue determination of antibiotics in bovine milk by liquid chromatography-tandem mass spectrometry: Combining efficiency of milk control and simplicity of routine analysis

被引:32
|
作者
Martins, Magda Targa [1 ,2 ]
Barreto, Fabiano [1 ,2 ]
Hoff, Rodrigo Barcellos [1 ,3 ]
Jank, Louise [1 ,3 ]
Arsand, Juliana Bazzan [1 ,3 ]
Campos Motta, Tanara Magalhaes [1 ,3 ]
Scherman Schapoval, Elfrides Eva [2 ]
机构
[1] Lab Nacl Agr LANAGRO RS, Minist Agr Pecuaria & Abastecimento, Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, Fac Farm, Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande do Sul, Inst Quim, Porto Alegre, RS, Brazil
关键词
HOT-WATER EXTRACTION; SAMPLE PREPARATION; HORWITZ-EQUATION; SCREENING METHOD; DRUG RESIDUES; LC-MS/MS; COW MILK; TETRACYCLINE; MUSCLE; LIMITATIONS;
D O I
10.1016/j.idairyj.2016.02.048
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Antibiotics are widely used in veterinary medicine and incorrect practices may lead to drug residues in food, including milk. Fast and simple sample preparation methods have been developed for determination of quinolones, fluoroquinolones, tetracyclines, sulphonamides, trimethoprim and bromexine using liquid chromatography-tandem mass spectrometry. Small volumes of sample (0.5 mL) were extracted using organic solvent followed by centrifugation and evaporation and/or dilution. Validation took into account the maximum residue limits (MRLs). Recoveries of 62-108% were obtained. Linearity (r(2)) above 0.96 was achieved for all compounds using concentrations in the range 0.25-2.0 x MRL. Intraday precision with coefficients of variation (n = 6) lower than 15.0% and inter-day precision lower than 17.3% were obtained for three concentration levels in the range 0.5-1.5 x MRL. Accuracy was 87 -108%. Limits of detection and quantitation, as well as decision limit, detection capability, robustness and applicability, were evaluated using >600 real milk samples. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:44 / 51
页数:8
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