High-throughput method for macrolides and lincosamides antibiotics residues analysis in milk and muscle using a simple liquid-liquid extraction technique and liquid chromatography-electrospray-tandem mass spectrometry analysis (LC-MS/MS)

被引:85
作者
Jank, Louise [1 ,2 ]
Martins, Magda Targa [1 ,3 ]
Arsand, Juliana Bazzan [1 ,2 ]
Campos Motta, Tanara Magalhaes [2 ]
Hoff, Rodrigo Barcellos [1 ,2 ]
Barreto, Fabiano [1 ,3 ]
Pizzolato, Tania Mara [1 ]
机构
[1] Univ Fed Rio Grande do Sul, PPGQ, Porto Alegre, RS, Brazil
[2] Minist Agr Pecuaria & Abastecimento, Lab Nacl Agr LANAGRO RS, Porto Alegre, RS, Brazil
[3] Univ Fed Rio Grande do Sul, PPGCF, Porto Alegre, RS, Brazil
关键词
LC-MS/MS; Antibiotics; Milk; Muscle; Residues; Macrolides; Lincosamides; SOLID-PHASE EXTRACTION; MULTI-RESIDUE; SOLVENT-EXTRACTION; VETERINARY DRUGS; CONFIRMATORY METHOD; SCREENING METHOD; CHICKEN MUSCLE; ANIMAL-TISSUES; BOVINE MUSCLE; WATER SAMPLES;
D O I
10.1016/j.talanta.2015.06.078
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A fast and simple method for residue analysis of the antibiotics classes of macrolides (erythromycin, azithromycin, tylosin, tilmicosin and spiramycin) and lincosamides (lincomycin and clindamycin) was developed and validated for cattle, swine and chicken muscle and for bovine milk. Sample preparation consists in a liquid-liquid extraction (LLE) with acetonitrile, followed by liquid chromatography-electrospray-tandem mass spectrometry analysis (LC-ESI-MS/MS), without the need of any additional cleanup steps. Chromatographic separation was achieved using a C18 column and a mobile phase composed by acidified acetonitrile and water. The method was fully validated according the criteria of the Commission Decision 2002/657/EC. Validation parameters such as limit of detection, limit of quantification, linearity, accuracy, repeatability, specificity, reproducibility, decision limit (CC alpha) and detection capability (CC beta) were evaluated. All calculated values met the established criteria. Reproducibility values, expressed as coefficient of variation, were all lower than 19.1%. Recoveries range from 60% to 107%. Limits of detection were from 5 to 25 mu g kg(-1).The present method is able to be applied in routine analysis, with adequate time of analysis, low cost and a simple sample preparation protocol. (C) 2015 Published by Elsevier B.V.
引用
收藏
页码:686 / 695
页数:10
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