Single-step multiresidue determination of ten multiclass veterinary drugs in pork, milk, and eggs using liquid chromatography with tandem mass spectrometry


Park J., Zhang D., Kim D., Kim S., Cho K., Jeong D., ...Daha Fazla

JOURNAL OF SEPARATION SCIENCE, cilt.38, sa.16, ss.2772-2780, 2015 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 38 Sayı: 16
  • Basım Tarihi: 2015
  • Doi Numarası: 10.1002/jssc.201500501
  • Dergi Adı: JOURNAL OF SEPARATION SCIENCE
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.2772-2780
  • Anahtar Kelimeler: Animal food products, Liquid-phase extraction, Multiresidue analysis, Tandem mass spectrometry, Veterinary drugs, CHICKEN MUSCLE, RESIDUES, VALIDATION, EXTRACTION, BOVINE, LC, PORCINE, QUICK, CHEAP
  • Atatürk Üniversitesi Adresli: Hayır

Özet

A multiclass, multiresidue determination method is reported for the detection of ten veterinary drugs, including scopolamine, metoclopramide, acriflavine, berberine, tripelennamine, diphenhydramine, acrinol, triamcinolone, loperamide, and roxithromycin in pork, milk, and eggs. The method involves a simple extraction using 0.1% formic acid in acetonitrile, followed by defatting with n-hexane, centrifugation, and filtration prior to liquid chromatography with tandem mass spectrometric analysis. As ion suppression and enhancement effects are reported, matrix-matched calibrations are used for quantification, with determination coefficients >= 0.9765. For the majority of the tested analytes, the intra-and interday accuracy (expressed as recovery %) range from 70.6 to 94.6% and from 70.1 to 93.3%, respectively, and the precision (expressed as relative standard deviation) ranges from 0.5 to 19.8% and from 2.8 to 18.4% in allmatrices. The limits of quantification range between 0.5 and 10 ng/g. The validated tandem mass spectrometry method is successfully applied to market samples; the target analytes are not detected in any of the tested samples. In terms of accuracy, no extract cleanup is deemed necessary. The developed method is feasible for the simultaneous detection of the tested analytes in pork, milk, and eggs.