4.7 Article

Determination of aminoglycoside residues in milk and muscle based on a simple and fast extraction procedure followed by liquid chromatography coupled to tandem mass spectrometry and time of flight mass spectrometry

期刊

TALANTA
卷 154, 期 -, 页码 38-45

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.talanta.2016.03.045

关键词

Aminoglycosides; Residues; Milk; Muscle; LC-MS/MS; Time of flight mass spectrometry

资金

  1. Capes Foundation - Brazilian Ministry of Education (CAPES)
  2. National Council for Scientific and Technological Development (CNPq)
  3. Brazilian Ministry of Agriculture, Livestock and Supply
  4. CAPES
  5. CNPq in PVE

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Antibiotics are widely used in veterinary medicine mainly for treatment and prevention of diseases. The aminoglycosides are one of the antibiotics classes that have been extensively employed in animal husbandry for the treatment of bacterial infections, but also as growth promotion. The European Union has issued strict Maximum Residue Levels (MRLs) for aminoglycosides in several animal origin products including bovine milk, bovine, swine and poultry muscle. This paper describes a fast and simple analytical method for the determination of ten aminoglycosides (spectinomycin, tobramycin, gentamicin, kanamycin, hygromycin, apramycin, streptomycin, dihydrostreptomycin, amikacin and neomycin) in bovine milk and bovine, swine and poultry muscle. For sample preparation, an extraction method was developed using trichloroacetic acid and clean up with low temperature precipitation and C18 bulk. Liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) was used to carry out quantitative analysis and liquid chromatography-quadrupole-time of flight-mass spectrometry (LC-QTOF-MS) was used to screening purposes. Both methods were validated according to the European Union Commission Directive 2002/657/EC. Good performance characteristics were obtained for recovery, precision, calibration curve, specificity, decision limits (CC alpha) and detection capabilities (CC beta) in all matrices evaluated. The detection limit (LOD) and quantification limit (LOQ) were ranging from 5 to 100 ng g(-1) and 12.5 to 250 ng g(-1), respectively. Good linearity (r)-above 0.99-was achieved in concentrations ranging from 0.0 to 2.0 x MRL. Recoveries ranged from 36.8% to 98.0% and the coefficient of variation from 0.9 to 20.2%, noting that all curves have been made into their own matrices in order to minimize the matrix effects. The CC beta values obtained in qualitative method were between 25 and 250 ng g(-1). The proposed method showed to be simple, easy, and adequate for high-throughput analysis of a large number of samples per day at low cost. (c) 2016 Elsevier B.V. All rights reserved.

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