Residual detection of naproxen, methyltestosterone and 17α-hydroxyprogesterone caproate in aquatic products by simple liquid–liquid extraction method coupled with liquid chromatography–tandem mass spectrometry

Zheng W., Yoo K., Choi J., Park D., Kim S., Kang Y., ...Daha Fazla

Biomedical Chromatography, cilt.33, sa.1, 2019 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 33 Sayı: 1
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1002/bmc.4396
  • Dergi Adı: Biomedical Chromatography
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Anahtar Kelimeler: 17 alpha-hydroxyprogesterone carproate, aquatic product, LC-MS/MS, methyltestosterone, naproxen, residue, NONSTEROIDAL ANTIINFLAMMATORY DRUGS, ANABOLIC-STEROIDS RESIDUES, SOLID-PHASE EXTRACTION, QUANTITATIVE-DETERMINATION, PHARMACEUTICAL RESIDUES, MUSCLE-TISSUES, RAINBOW-TROUT, PRETERM BIRTH, ANIMAL MUSCLE, PERFORMANCE
  • Atatürk Üniversitesi Adresli: Evet

Özet

© 2018 John Wiley & Sons, Ltd.In the present study, we aimed to develop a reliable screening method based on liquid chromatography coupled with tandem mass spectrometry (LC–MS/MS) for the detection and quantification of naproxen, methyltestosterone and 17α-hydroxyprogesterone caproate residues. The target analytes were extracted from samples of eel, flatfish and shrimp using acetonitrile with 1% acetic acid, followed by liquid–liquid purification with n-hexane. Chromatographic separation was achieved on a reversed-phase analytical column using 0.1% formic acid containing 10 mm ammonium formate in distilled water (A) and methanol (B) as mobile phases. All the matrix-matched calibration curves were linear (R2 ≥ 0.99) over the concentration range of the tested analytes. Recovery at three spiking levels (0.005, 0.01 and 0.02 mg/kg) ranged from 68 to 117% with intra- and inter-day precisions <10%. Five market samples for each matrix (eel, flatfish and shrimp) were collected and tested for method application. In summary, the proposed method is feasible to screen and quantify the analytes with high selectivity in aquatic food products meant for human consumption.