Simultaneous Determination of 15 Antibiotics Residues in Milk by Liquid Chromatography Tandem Mass Spectrometry
LI Yifa
Abstract
LI Yifa
Abstract
A new approach for the simultaneous determination of residues of three classes of antibiotics, i.e., penicillins, sulfoamides and tetracyclines, in milk by ultra performance liquid chromatographytandem mass spectrometry(UPLC-MSMS) was established. Samples were extracted with acetonitrile-water(3:1, V/V), cleaned up using an HLB SPE cartridge and blown to dryness under nitrogen and the residues were then dissolved in 1.0 m L of mobile phase. A total of 15 analytes were separated on ZORBAX Ecliplus C18 column with a mobile phase composed of acetonitrile and 5 mmol/L formic ammonium acetate solution containing 0.2% formic acid with gradient elution, detected by ESI-MS/MS and quantified by the external standard method. The correlation coefficients of the linear calibration curves were over 0.999 in the corresponding concentration range. The average recoveries of the 15 analytes ranged from 75.1% to 103.7%, with relative standard deviations(RSDs) at three spiked concentrations of 1.4%–7.3%. The limit of detection(LOD, RSN≥3) and quantification(LOQ, RSN ≥ 10) were 0.2–4.0 and 1.0–4.0 μg/kg, respectively. The new method is simple, fast, sensitive and reliable, and it is suitable for the determination of antibiotic residues in milk.
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A new approach for the simultaneous determination of residues of three classes of antibiotics, i.e., penicillins, sulfoamides and tetracyclines, in milk by ultra performance liquid chromatographytandem mass spectrometry(UPLC-MSMS) was established. Samples were extracted with acetonitrile-water(3:1, V/V), cleaned up using an HLB SPE cartridge and blown to dryness under nitrogen and the residues were then dissolved in 1.0 m L of mobile phase. A total of 15 analytes were separated on ZORBAX Ecliplus C18 column with a mobile phase composed of acetonitrile and 5 mmol/L formic ammonium acetate solution containing 0.2% formic acid with gradient elution, detected by ESI-MS/MS and quantified by the external standard method. The correlation coefficients of the linear calibration curves were over 0.999 in the corresponding concentration range. The average recoveries of the 15 analytes ranged from 75.1% to 103.7%, with relative standard deviations(RSDs) at three spiked concentrations of 1.4%–7.3%. The limit of detection(LOD, RSN≥3) and quantification(LOQ, RSN ≥ 10) were 0.2–4.0 and 1.0–4.0 μg/kg, respectively. The new method is simple, fast, sensitive and reliable, and it is suitable for the determination of antibiotic residues in milk.
Key concepts: Chromatography, Chemistry, Formic acid, Detection limit, Ammonium acetate, Analyte, Liquid chromatography–mass spectrometry, Mass spectrometry