An LC-ESI-MS/MS method for residues of fluoroquinolones, sulfonamides, tetracyclines and trimethoprim in feedingstuffs: validation and surveillance

被引:20
作者
Jank, Louise [1 ,2 ]
Martins, Magda Targa [1 ]
Arsand, Juliana Bazzan [1 ,2 ]
Ferrao, Marco Flores [2 ]
Hoff, Rodrigo Barcellos [1 ]
Barreto, Fabiano [1 ]
Pizzolato, Tania Mara [2 ]
机构
[1] Lab Nacl Agr LANAGRO RS, Residue Anal Lab, Porto Alegre, RS, Brazil
[2] Univ Fed Rio Grande do Sul, PPGQ, Porto Alegre, RS, Brazil
来源
FOOD ADDITIVES AND CONTAMINANTS PART A-CHEMISTRY ANALYSIS CONTROL EXPOSURE & RISK ASSESSMENT | 2018年 / 35卷 / 10期
关键词
LC-MS; MS; antimicrobials; feedingstuffs; veterinary drug residues; fluoroquinolones; sulfonamides; RESOLUTION MASS-SPECTROMETRY; ANTIBIOTIC-RESISTANCE GENES; LIQUID-CHROMATOGRAPHY; VETERINARY DRUGS; MULTICLASS METHOD; PLANT TOXINS; ANIMAL FEED; EXTRACTION; FOOD; COCCIDIOSTATS;
D O I
10.1080/19440049.2018.1508895
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
An increasing concern about food safety has been observed over the years. The presence of drugs residues in food is one of the major subjects of research in food safety. Feedingstuffs can be responsible for carryover into the food chain of residues of several drugs. This paper describes the development, validation and application of a fast and simple method for analysis of 24 antibiotic residues in feedingstuffs for cattle, pigs and poultry. Analytes include compounds from different antimicrobials classes, such as sulfonamides (sulfadiazine, sulfamethazine, sulfamethoxazole, sulfaquinoxaline, sulfachlorpyridazine, sulfadoxine, sulfadimethoxine, sulfizoxazole, sulfamerazine and sulfathiazole), fluoroquinolones (ciprofloxacin, enrofloxacin, norfloxacin, danofloxacin, difloxacin, sarafloxacin, flumequine, nalidixic acid and oxolinic acid), tetracyclines (tetracycline, doxycycline, oxytetracycline and chlortetracycline) and trimethoprim. Samples were extracted with methanol:water (70:30) 0.1% formic acid, followed by clean-up steps using centrifugation, low-temperature purification (LTP) and ultracentrifugation. Instrumental analysis was performed using liquid chromatography coupled to tandem mass spectrometry. Chromatographic separation was achieved using a C18 column and a mobile phase composed of acetonitrile and water, both with 0.1% formic acid. Validation parameters such as limit of detection (LOD), limit of quantification (LOQ), selectivity, linearity, accuracy, precision, decision limit (CC) and detection capability (CC) were determined and meet the adopted criteria. LOD and LOQ were set to 30 and 75 mu g kg(-1), respectively. Inter-day precision were in the range from 4.0 to 11.1%, and linearity provides values of r(2) above 0.95 for all analytes. The optimised method was applied to the analysis of more than 1500 real samples within the period 2012-2017. Non-compliant results were discussed and classified in terms of analytes, feed types and target species. Multivariate analysis of the data was performed using principal component analysis.
引用
收藏
页码:1975 / 1989
页数:15
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