Application of cloud point extraction for residues of chloramphenicol and amoxicillin in milk samples by HPLC-DAD

Sürücü B., Ulusoy H. İ., Ulusoy S., Demir O., Gulle S.

EUROPEAN FOOD RESEARCH AND TECHNOLOGY, cilt.248, sa.2, ss.437-445, 2022 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 248 Sayı: 2
  • Basım Tarihi: 2022
  • Doi Numarası: 10.1007/s00217-021-03889-6
  • Dergi Adı: EUROPEAN FOOD RESEARCH AND TECHNOLOGY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, ABI/INFORM, Agricultural & Environmental Science Database, Aquatic Science & Fisheries Abstracts (ASFA), BIOSIS, Biotechnology Research Abstracts, CAB Abstracts, Chemical Abstracts Core, Compendex, Food Science & Technology Abstracts, Hospitality & Tourism Complete, Hospitality & Tourism Index, Veterinary Science Database
  • Sayfa Sayıları: ss.437-445
  • Anahtar Kelimeler: Amoxicillin, Chloramphenicol, PEG-6000, HPLC, Cloud point extraction, Milk samples, SOLID-PHASE EXTRACTION, TETRACYCLINE, SULFONAMIDES, SORBENT, PLASMA, DRUGS
  • Sivas Cumhuriyet Üniversitesi Adresli: Evet

Özet

A pre-concentration and sensitive determination method for residues of Chloramphenicol (CLP) and Amoxicillin (AMX) in milk samples were developed based on cloud point extraction (CPE) and HPLC-DAD analysis. CLP and AMX molecules were extracted to surfactant phases of polyethylene glycol-6000 (PEG-6000) in the presence of pH 7.0 buffer and high electrolyte concentration. Experimental variables were examined and optimized such as concentration of electrolyte and surfactant, pH, incubation time, and diluting solvent. In the developed method, determination of CLP and AMX using HPLC system was carried out by isocratic elution of water:acetonitrile (30:70) mixture. CLP and AMX antibiotic molecules were analyzed by considering peak area obtained by DAD detector at 273 nm and 276 nm, respectively. After optimization experimental variables, analytical signals were linear in the range of 10-900 ng mL(-1) and 25-1000 ng mL(-1), respectively. The limit of detection values was calculated as 2.98 and 7.46 ng mL(-1) while relative standard deviations (RSD %) were lower than 4.20% for 100 ng mL(-1). Finally, the developed method was successively applied to cow milk samples.