Voltammetric determination of pyridoxine (Vitamin B"6) at a carbon paste electrode modified with vanadyl(IV)-Salen complex [An article from: Analytica Chimica Acta]
Book Details
PublisherElsevier
ISBN / ASINB000RR00VA
ISBN-13978B000RR00V2
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Description
This digital document is a journal article from Analytica Chimica Acta, published by Elsevier in 2004. The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.
Description:
The preparation and electrochemical characterization of a carbon paste electrode modified with the N,N-ethylene-bis(salicylideneiminato)oxovanadium(IV) complex [VO(Salen)] as well as its behavior in relation to the oxidation of pyridoxine (Vitamin B"6) are described. The electrochemical behavior of the modified electrode and the electrooxidation of pyridoxine were investigated using cyclic voltammetry. The best voltammetric response was obtained for an electrode composition of 15% (m/m) [VO(Salen)] in the paste, KCl solution of pH 5.5-8.0 and scan rate of 25mVs^-^1. A sensitive linear voltammetric response for pyridoxine was obtained in the concentration range of 4.5x10^-^4 to 3.3x10^-^3moll^-^1 with a slope of 42.5@mAmmol^-^1l, and a detection limit (3@s/slope) of 3.7x10^-^5moll^-^1 using linear sweep voltammetry. Among several compounds tested only Vitamin B"1 seems to interfere in the analyte signal. The concentrations of pyridoxine in pharmaceutical formulations using the proposed electrode and an official spectrophotometric method based in the reaction with N,N-diethyl-p-phenylenediamine are in agreement at the 95% confidence level and within an acceptable range of error.
Description:
The preparation and electrochemical characterization of a carbon paste electrode modified with the N,N-ethylene-bis(salicylideneiminato)oxovanadium(IV) complex [VO(Salen)] as well as its behavior in relation to the oxidation of pyridoxine (Vitamin B"6) are described. The electrochemical behavior of the modified electrode and the electrooxidation of pyridoxine were investigated using cyclic voltammetry. The best voltammetric response was obtained for an electrode composition of 15% (m/m) [VO(Salen)] in the paste, KCl solution of pH 5.5-8.0 and scan rate of 25mVs^-^1. A sensitive linear voltammetric response for pyridoxine was obtained in the concentration range of 4.5x10^-^4 to 3.3x10^-^3moll^-^1 with a slope of 42.5@mAmmol^-^1l, and a detection limit (3@s/slope) of 3.7x10^-^5moll^-^1 using linear sweep voltammetry. Among several compounds tested only Vitamin B"1 seems to interfere in the analyte signal. The concentrations of pyridoxine in pharmaceutical formulations using the proposed electrode and an official spectrophotometric method based in the reaction with N,N-diethyl-p-phenylenediamine are in agreement at the 95% confidence level and within an acceptable range of error.
