Metal organic framework/clay composite for micro-dispersive solid-phase extraction of sulfonamides and penicillins in milk, and synthetic urine solution coupling with HPLC/DAD detection


Saad Aldoori M., MERDİVAN M., ALTINIŞIK TAĞAÇ A.

Microchemical Journal, cilt.184, 2023 (SCI-Expanded, Scopus) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 184
  • Basım Tarihi: 2023
  • Doi Numarası: 10.1016/j.microc.2022.108165
  • Dergi Adı: Microchemical Journal
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, BIOSIS, CAB Abstracts, Chemical Abstracts Core, Chimica, Food Science & Technology Abstracts, Index Islamicus, Veterinary Science Database
  • Anahtar Kelimeler: MMT, MOF, mu-dSPE, Antibiotics, HPLC
  • Dokuz Eylül Üniversitesi Adresli: Evet

Özet

In this study, composite as a copper-containing metal–organic framework with montmorillonite (MMT) clay was synthesized and applied as an adsorbent for micro-dispersive solid-phase extraction (µ-dSPE) of sulfonamides (SAs) and penicillins (PENs). The synthesized composites including different content of MMT were characterized by Fourier transform infrared spectroscopy, X-ray diffraction, scanning electron microscopy, Brunauer-Emmett–Teller surface area, and thermogravimetric analysis. The determination of antibiotics was performed by high-performance liquid chromatography/diode array detection (HPLC/DAD) using C18 column as stationary phase, 0.1 % trifluoroacetic acid in water, and acetonitrile as mobile phase in gradient mode and detection at 270 nm for SAs and 230 nm for PENs. The as-synthesized composites were examined for their adsorption ability towards target antibiotics. The optimized parameter conditions were 10 mg of adsorbent, 5 mL of sample solution at pH 4, 10 min stirring by vortex, 1 mL of acetonitrile:methanol (1:1) as eluent solvent, and 5 min as elution time. Under optimized conditions, the proposed method presented good linearity from 0.5 to 400 µg/L for SAs and from 1 to 400 µg/L for PENs with coefficients of determination (r2) ≥ 0.9947, low limit of detections from 0.10 to 0.15 µg/L for SAs and 0.30 to 1.50 µg/L for PENs, acceptable repeatabilities less than 3.26 % for both groups and good recoveries from 82.3 % to 116.4 % with relative standard deviations less than 3.9 % for both groups in the spiked milk samples and synthetic urine solution. The developed µ-dSPE method following HPLC/DAD has been successfully applied to the determination of SAs and PENs milk samples and synthetic urine solutions.