Validation of a liquid chromatography-tandem mass spectrometry screening method to monitor 58 antibiotics in milk: a qualitative approach

被引:81
作者
Gaugain-Juhel, M. [1 ]
Delepine, B. [1 ]
Gautier, S. [1 ]
Fourmond, M. P. [1 ]
Gaudin, V. [1 ]
Hurtaud-Pessel, D. [1 ]
Verdon, E. [1 ]
Sanders, P. [1 ]
机构
[1] Agence Francaise Secur Sanit Aliments, Community Reference Lab Antimicrobiol Residues, Lab Etud & Rech Medicaments Vet & Desinfectants, F-35302 La Haute Marche, Fougeres, France
来源
FOOD ADDITIVES AND CONTAMINANTS PART A-CHEMISTRY ANALYSIS CONTROL EXPOSURE & RISK ASSESSMENT | 2009年 / 26卷 / 11期
关键词
in-house validation; liquid chromatography; mass spectrometry (LC; MS); method validation; statistical analysis; veterinary drug residues-antibiotics; milk; VETERINARY DRUGS; UPLC-TOF; RESIDUES;
D O I
10.1080/02652030903150575
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A multi-residue method was developed for monitoring antibiotic residues in milk using liquid chromatography coupled to a tandem quadrupole mass spectrometer (LC/MS-MS). Two very short extractions followed by two LC/MS-MS acquisitions allowed the screening of 58 antibiotics belonging to eight different families (penicillins, cephalosporins, sulfonamides, macrolides, lincosamides, aminoglycosides, tetracyclines, and quinolones). This method is currently implemented in the laboratory in a qualitative way, i.e. monitoring the presence or absence of residue in a sample and identification of the analyte before the confirmation step. In order to assess the performance of this method, a validation strategy described in an internal guideline for the validation of screening methods was applied. The aim of the validation was to prove sufficient sensitivity of the method to detect all the targeted antibiotics at the level of interest (maximum residue limit, MRL) at least. According to European Commission Decision 2002/657/EC, the suitable sensitivity of a screening method can be demonstrated when the CC is below or equal to the MRL and so the false-compliant rate below or equal to 5% at the MRL level. The validation scheme was established in order to take into account various variability factors: the apparatus response, the interday repeatability, the matrix effect, etc. The results of the validation clearly demonstrate the suitability of this method for the detection and identification of more than 50 antibiotics and they are in agreement with the results obtained in routine analysis.
引用
收藏
页码:1459 / 1471
页数:13
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