Firstly electrochemical investigetions and determination of anticoagulant drug edoxaban at single-use pencil graphite electrode: an eco-friendly and cost effective voltammetric method

Yükleniyor...
Küçük Resim

Tarih

2023

Dergi Başlığı

Dergi ISSN

Cilt Başlığı

Yayıncı

Springer Science and Business Media Deutschland GmbH

Erişim Hakkı

info:eu-repo/semantics/closedAccess

Özet

Objectives: The anticoagulant drug edoxaban has a blood thinning mechanism of action. In this study, a pencil graphite electrode was electrochemically activated at + 1.4 V for 60 s. in a Britton-Robinson (pH 9.0) supporting electrolyte solution. Evidence acquisition: A simple, fast, and sensitive electrochemical procedure was developed using cyclic voltammetry and square wave voltammetry techniques. It was observed that edoxaban gave a good oxidation signal with cyclic voltammetry technique at a potential of + 0.98 V (vs. Ag/AgCl). Results: This procedure showed a linear response in a Britton-Robinson (pH 9.0) media within the concentration range of 0.2–1.8 µM and limit of detection (LOD) and the limit of quantification (LOQ) values were determined to be 0.073 μM (0.133 μg mL−1) and 0.243 μM (0.443 μg mL−1), respectively. Conclusion: The method developed in this study was successfully applied to drug and urine samples. The developed voltammetric method was highly selective and gave satisfactory recovery results in urine and pharmaceutical samples. The results of the voltammetric method were compared with the spectroscopic method and it was determined that the results were compatible.

Açıklama

Anahtar Kelimeler

Anticoagulant, Edoxaban, Pencil graphite electrode, Voltammetry

Kaynak

DARU, Journal of Pharmaceutical Sciences

WoS Q Değeri

N/A

Scopus Q Değeri

Q1

Cilt

31

Sayı

2

Künye

Kılıç, A., Aslan, M., Önal, G. ve Levent, A. (2023). Firstly electrochemical investigetions and determination of anticoagulant drug edoxaban at single-use pencil graphite electrode: an eco-friendly and cost effective voltammetric method. DARU, Journal of Pharmaceutical Sciences, 31(2), 233-241.