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Merck
  • Determination of selected veterinary antimicrobials in poultry excreta by UHPLC-MS/MS, for application in Salmonella control programs.

Determination of selected veterinary antimicrobials in poultry excreta by UHPLC-MS/MS, for application in Salmonella control programs.

Analytical and bioanalytical chemistry (2015-01-31)
Brecht Gorissen, Tim Reyns, Mathias Devreese, Patrick De Backer, Joris Van Loco, Siska Croubels
要旨

The most important source of Salmonella spp. infection in humans is by the consumption of contaminated poultry products. Due to the risk of resistance development and its transfer from animals to humans, the Belgian Royal Decree concerning the eradication of Salmonella (C-2007/22784) prohibits treatment of poultry with antimicrobials against zoonotic Salmonella spp. To uncover illicit use, an analytical method using ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) for the determination of antimicrobial residues in poultry excreta was developed and validated for classes having an active spectrum against Salmonella spp. in poultry: β-lactams (amoxicillin and penicillin V), fluoroquinolones (enrofloxacin, difloxacin, and flumequine), polymyxins (colistin), sulfonamides in combination with trimethoprim (sulfachloropyridazine, sulfadiazine, and sulfaclozine), and tetracyclines (chlortetracycline and doxycycline). A generic and high-throughput sample preparation was developed. Extraction of samples was performed by ultrasonication using a combination of acetonitrile and McIlvaine buffer, followed by centrifugation and filtration prior to analysis. The method was validated according to Commission Decision 2002/657/EC for linearity, apparent recovery/trueness, repeatability, reproducibility, limit of quantification, limit of detection, specificity, matrix effect, and storage stability in matrix. To demonstrate the applicability of the method, an in vivo experiment was conducted. For each antimicrobial class, one registered drug was selected and administered in the drinking water to two laying hens. Excreta samples were collected every 12 h during and until 2 days after treatment and analyzed using the developed method.

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製品内容

Sigma-Aldrich
ドキシサイクリン ハイクレート
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リン酸ナトリウム 二塩基性 二水和物, BioUltra, for molecular biology, ≥99.0% (T)
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ドキソルビシン 塩酸塩, 98.0-102.0% (HPLC)
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アンピシリン, anhydrous, 96.0-102.0% (anhydrous basis)
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トリメトプリム, ≥98.5%
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ドキソルビシン 塩酸塩, suitable for fluorescence, 98.0-102.0% (HPLC)
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クエン酸, ≥99.5%, FCC, FG
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カリウム, chunks (in mineral oil), 98% trace metals basis
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クエン酸, anhydrous, suitable for cell culture, suitable for plant cell culture
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トリメトプリム, ≥99.0% (HPLC)
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水素化カリウム, 30 wt % dispersion in mineral oil
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クエン酸, BioUltra, anhydrous, ≥99.5% (T)
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クロルテトラサイクリン 塩酸塩, ≥91.0% dry basis (HPLC)
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クエン酸, ACS reagent, ≥99.5%
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ギ酸, ≥95%, FCC, FG
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スルファジアジン, 99.0-101.0%
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クエン酸, 99%
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2-Hydroxybutyric acid sodium salt, 97%
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水素化カリウム, in paraffin
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ギ酸, JIS special grade, ≥98.0%
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スルファヘナゾール, ≥98%
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クロルテトラサイクリン 塩酸塩, BioReagent, suitable for fluorescence, from Streptomyces aureofaciens, ≥85.0% (HPLC)
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デメクロサイクリン 塩酸塩, powder or crystals
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クエン酸, anhydrous, free-flowing, Redi-Dri, ACS reagent, ≥99.5%
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Ampicillin, meets USP testing specifications
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クエン酸, SAJ first grade, ≥99.5%
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ギ酸, SAJ first grade, 88.0-89.5%