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Target screening of 105 veterinary drug residues in milk using UHPLC/ESI Q-Orbitrap multiplexing data independent acquisition.
Wang, Jian; Leung, Daniel; Chow, Willis; Chang, James; Wong, Jon W.
Afiliação
  • Wang J; Calgary Laboratory, Canadian Food Inspection Agency, 3650-36th Street N.W, Calgary, Alberta, T2L 2L1, Canada. jian.wang@inspection.gc.ca.
  • Leung D; Calgary Laboratory, Canadian Food Inspection Agency, 3650-36th Street N.W, Calgary, Alberta, T2L 2L1, Canada.
  • Chow W; Calgary Laboratory, Canadian Food Inspection Agency, 3650-36th Street N.W, Calgary, Alberta, T2L 2L1, Canada.
  • Chang J; ThermoFisher Scientific, 355 River Oaks Parkway, San Jose, CA, 95134, USA.
  • Wong JW; Center for Food Safety and Applied Nutrition, US Food and Drug Administration, 5100 Campus Drive, College Park, MD, 20740, USA.
Anal Bioanal Chem ; 410(22): 5373-5389, 2018 Sep.
Article em En | MEDLINE | ID: mdl-29404665
ABSTRACT
This paper presents a multi-class target screening method for the detection of 105 veterinary drug residues from 11 classes in milk using ultra-high performance liquid chromatography electrospray ionization quadrupole Orbitrap mass spectrometry (UHPLC/ESI Q-Orbitrap). The method is based on a non-target approach of full mass scan and multiplexing data-independent acquisition (Full MS/mDIA). The veterinary drugs include endectocides, fluoroquinolones, ionophores, macrolides, nitroimidazole, NSAIDs, ß-lactams, penicillins, phenicols, sulfonamides, and tetracyclines. Veterinary drug residues were extracted from milk using a salting-out and solid-phase extraction (SOSPE) procedure, which entailed the precipitation of milk proteins by an extraction buffer (oxalic acid and EDTA, pH 3) and acetonitrile, a salting-out acetonitrile/water phase separation using ammonium sulfate, and solid-phase extraction for clean-up using polymeric reversed-phase sorbent cartridges. The Q-Orbitrap Full MS/dd-MS2 (data-dependent acquisition) was used to acquire product-ion spectra of individual veterinary drugs to build a compound database and a mass spectral library, whereas its Full MS/mDIA was utilized to acquire sample data from milk for target screening of veterinary drugs fortified at 1.0 or 10.0 µg/kg. The in-spectrum mass correction or solvent background lock-mass correction was used to minimize mass error when building the compound database from experimental dd-MS2 accurate mass data. Retention time alignment and response threshold adjustment were used to eliminate or reduce false negatives and/or false positive rates. The validated method was capable of screening 58% and 96% of 105 veterinary drugs at 1.0 and 10.0 µg/kg, respectively, without manually evaluating every compound during data processing, which will reduce the workload in routine practice.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Contaminação de Alimentos / Cromatografia Líquida de Alta Pressão / Drogas Veterinárias / Espectrometria de Massas por Ionização por Electrospray / Leite / Análise de Perigos e Pontos Críticos de Controle Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Animals Idioma: En Revista: Anal Bioanal Chem Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Contaminação de Alimentos / Cromatografia Líquida de Alta Pressão / Drogas Veterinárias / Espectrometria de Massas por Ionização por Electrospray / Leite / Análise de Perigos e Pontos Críticos de Controle Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Animals Idioma: En Revista: Anal Bioanal Chem Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Canadá