Determination of tramadol in pharmaceutical forms and urine samples using a boron-doped diamond electrode

Keskin E., Allahverdiyeva S., Seyho E., Yardım Y.

JOURNAL OF THE SERBIAN CHEMICAL SOCIETY, cilt.85, sa.7, ss.923-937, 2020 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 85 Sayı: 7
  • Basım Tarihi: 2020
  • Doi Numarası: 10.2298/jsc190906138k
  • Dergi Adı: JOURNAL OF THE SERBIAN CHEMICAL SOCIETY
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Aerospace Database, Aquatic Science & Fisheries Abstracts (ASFA), CAB Abstracts, Central & Eastern European Academic Source (CEEAS), Chemical Abstracts Core, Communication Abstracts, Food Science & Technology Abstracts, Metadex, Directory of Open Access Journals, Civil Engineering Abstracts
  • Sayfa Sayıları: ss.923-937
  • Van Yüzüncü Yıl Üniversitesi Adresli: Evet

Özet

The present work describes the electroanalytical investigation and a novel voltammetric method for the cheap, fast and simple quantification of tramadol (TRH) using a boron-doped diamond electrode. TRH displayed one well-defined, irreversible and adsorption-controlled oxidation peak at about 1.58 V (vs. Ag/AgCl) in Britton-Robinson buffer (BR, 0.1 mol L-1, pH 3.0) using the cyclic voltammetry technique. The voltammetric responses of the oxidation peaks are dependent on pH and their sensitivity was significantly enhanced in the presence of surfactant media (sodium dodecyl sulphate, SDS). Under the optimized experiment conditions, employing the square-wave stripping mode, it was found that there was an excellent correlation between oxidation peak current and the TRH concentration in the range 0.25 to 50.0 mu g mL(-1) (8.34 x 10(-7)-1.67 x 10(-4) mol L-1), with a detection limit of 0.072 mu g mL(-1) (2.40 x 10(-7) mol L-1) in 0.1 mol L-1 BR buffer (pH 3.0) solution comprising 8 x 10(-4) mol L-1 SDS at 1.52 V (after 30 s accumulation at open-circuit conditions). The developed approach could be used for the quantification of TRH in pharmaceutical formulations and spiked human urine samples with acceptable recoveries.