W. Oungpipat et al., FLOW-INJECTION DETECTION OF TETRACYCLINES BY ELECTROCATALYTIC OXIDATION AT A NICKEL-MODIFIED GLASSY-CARBON ELECTRODE, Analyst, 120(5), 1995, pp. 1559-1565
The electrocatalytic oxidation of tetracyclines in an alkaline solutio
n at a nickel-modified glassy carbon electrode was investigated. The r
esponse of the modified electrode was characterized by voltammetry and
flow injection. Subsequently, it was used for amperometric detection
of tetracyclines in a flow injection system. The preparation of the mo
dified electrode is carried out by simple deposition of Ni-II solution
onto the glassy carbon-based electrode. The detection is based on the
measurement of anodic current generated by the catalytic oxidation of
the antibiotics at the surface of the electrode through the formation
of a high-valent, oxyhydroxide species (NiOOH) at +550 V (versus Ag/A
gCI), The modified electrode offers a stable and reproducible catalyti
c oxidation current for these antibiotics without recourse to pulsed w
aveform potential. Rapid quantification at the mg l(-1) (ppm) level is
achieved. Standard calibration graphs for tetracycline, doxycycline,
oxytetracycline and chlortetracycline yielded linear ranges of 2.5-80,
2.5-100, 2.5-100 and 2.5-100 mg l(-1), respectively. Detection limits
(S/N = 3) of (0.03, 0.92, 0.34 and 1.81 mg l(-1) were obtained for te
tracycline, doxycycline, oxytetracycline and chlortetracycline, respec
tively, The electrode was applied for the determination of the four an
tibiotics in single-component drug formulations.