Electrochemical Determination and in silico Studies of Fludarabine on NH2 Functionalized Multiwalled Carbon Nanotube Modified Glassy Carbon Electrode

DOĞAN TOPAL B., BAKIRHAN N. K., TAŞKIN TOK T., Ozkan S. A.

Electroanalysis, cilt.32, sa.1, ss.37-49, 2020 (SCI-Expanded) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 32 Sayı: 1
  • Basım Tarihi: 2020
  • Doi Numarası: 10.1002/elan.201900347
  • Dergi Adı: Electroanalysis
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, Aerospace Database, Applied Science & Technology Source, BIOSIS, Chimica, Communication Abstracts, Metadex, Civil Engineering Abstracts
  • Sayfa Sayıları: ss.37-49
  • Anahtar Kelimeler: Fludarabine, nanosensor, multi walled carbon nanotubes, thermodynamic, molecular dynamics, MOLECULAR-DYNAMICS, ADENINE, GUANINE, TRIPHOSPHATE, QUANTIFICATION, IDENTIFICATION, NANOSENSORS, VOLTAMMETRY, OXIDATION, DOCKING
  • Ankara Üniversitesi Adresli: Evet

Özet

© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, WeinheimA sensitive voltammetric technique has been developed for the determination of Fludarabine using amine-functionalized multi walled carbon nanotubes modified glassy carbon electrode (NH2-MWCNTs/GCE). Molecular dynamics simulations, an in silico technique, were employed to examine the properties including chemical differences of Fludarabine- functionalized MWCNT complexes. The redox behavior of Fludarabine was examined by cyclic, differential pulse and square wave voltammetry in a wide pH range. Cyclic voltammetric investigations emphasized that Fludarabine is irreversibly oxidized at the NH2-MWCNTs/GCE. The electrochemical behavior of Fludarabine was also studied by cyclic voltammetry to evaluate both the kinetic (ks and Ea) and thermodynamic (ΔH, ΔG and ΔS) parameters on NH2-MWCNTs/GCE at several temperatures. The mixed diffusion-adsorption controlled electrochemical oxidation of Fludarabine revealed by studies at different scan rates. The experimental parameters, such as pulse amplitude, frequency, deposition potential optimized for square-wave voltammetry. Under optimum conditions in phosphate buffer (pH 2.0), a linear calibration curve was obtained in the range of 2×10−7 M–4×10−6 M solution using adsorptive stripping square wave voltammetry. The limit of detection and limit of quantification were calculated 2.9×10−8 M and 9.68×10−8 M, respectively. The developed method was applied to the simple and rapid determination of Fludarabine from pharmaceutical formulations.