The determination of rutin, quercetin and taxifolin in pharmaceutical dosage forms using cyclic voltammetry on multi-walled carbon nanotube modified glassy carbon electrode (MWNT-GCE) has been developed. The surface of the electrode created has been characterized by atomic force microscopy. Electrode modification with MWNT increases the surface average roughness (190-fold) and structures it. There are two oxidation steps at 0.22 and 0.80, 0.23 and 0.80, 0.26 and 0.86 V on cyclic voltammograms of taxifolin, quercetin and rutin, respectively, in phosphate buffer solution of pH 7.4. The linear dynamic range is 1.4–28 and 28–210, 2.0–220 and 0.52–210 μM with detection limits of 0.71, 1.0 and 0.26 μM for rutin, quercetin and taxifolin, respectively. The relative standard deviation of flavonoids determination in pharmaceuticals does not exceed of 7%. The data obtained are in good agreement with coulometric determination.
No takes yet. Share an insight, caveat, or question.
Ziyatdinova et al. (2011) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: