Premium
Electrochemical and Spectroelectrochemical Studies on Pyridoxine Hydrochloride Using a Poly(methylene blue) Modified Electrode
Author(s) -
Tan Liang,
Xie Qingji,
Yao Shouzhuo
Publication year - 2004
Publication title -
electroanalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.574
H-Index - 128
eISSN - 1521-4109
pISSN - 1040-0397
DOI - 10.1002/elan.200302993
Subject(s) - methylene blue , electrochemistry , cyclic voltammetry , electrode , chemistry , horizontal scan rate , detection limit , inorganic chemistry , adsorption , redox , pyridoxine hydrochloride , nuclear chemistry , pyridoxine , catalysis , organic chemistry , chromatography , photocatalysis , biochemistry
The electrochemical redox processes of pyridoxine hydrochloride (VB 6 ) at a poly(methylene blue) film modified glass carbon electrode (PMBE) in a phosphate buffer solution (PBS, pH 8.0) were studied by cyclic voltammetry. The VB 6 electrode reaction with quasi‐reversible characteristics was diffusion‐controlled at low scan rates and adsorption‐controlled at high scan rates. The anodic peak current positive to 0.6 V (vs. SCE) was found to be proportional to the concentration of VB 6 in the range of 0.010 to 1.03 mg⋅mL −1 with a detection limit of 1.34 μg mL −1 . Fluorescence and UV‐vis absorption spectroelectrochemical measurements suggest that the pyridine ring was not destroyed over the potential range from −0.8 to 1 V (vs. SCE), and the electrocatalytic generation of pyridoxal was anodically started at 0.57 V.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom