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  • 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
ABSTRACT

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.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Doxorubicin hydrochloride, suitable for fluorescence, 98.0-102.0% (HPLC)
Sigma-Aldrich
Trimethoprim, ≥99.0% (HPLC)
Sigma-Aldrich
di-Sodium hydrogen phosphate dihydrate, BioUltra, for molecular biology, ≥99.0% (T)
Sigma-Aldrich
Doxorubicin hydrochloride, 98.0-102.0% (HPLC)
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Trimethoprim, ≥98.5%
Sigma-Aldrich
Doxycycline hyclate
Sigma-Aldrich
Ampicillin, meets USP testing specifications
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Potassium hydride, in paraffin
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Citric acid, BioUltra, anhydrous, ≥99.5% (T)
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Chlortetracycline hydrochloride, suitable for fluorescence, BioReagent, from Streptomyces aureofaciens, ≥85.0% (HPLC)
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Potassium, chunks (in mineral oil), 98% trace metals basis
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Formic acid, ≥95%, FCC, FG
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Citric acid, ACS reagent, ≥99.5%
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2-Hydroxybutyric acid sodium salt, 97%
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Potassium hydride, 30 wt % dispersion in mineral oil
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Citric acid, ≥99.5%, FCC, FG
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Sulfaphenazole, ≥98%
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Ampicillin, anhydrous, 96.0-102.0% (anhydrous basis)
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Citric acid, 99%
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Chlortetracycline hydrochloride, ≥91.0% dry basis (HPLC)
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Sulfadiazine, 99.0-101.0%
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Demeclocycline hydrochloride, powder or crystals
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Citric acid, anhydrous, suitable for cell culture, suitable for plant cell culture
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Sulfaphenazole, ≥98% (HPLC)
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Citric acid, anhydrous, free-flowing, Redi-Dri, ACS reagent, ≥99.5%