Generic placeholder image

Current Pharmaceutical Analysis

Editor-in-Chief

ISSN (Print): 1573-4129
ISSN (Online): 1875-676X

Research Article

Kinetic of Rutin Degradation and its Determination in Dietary Supplements

Author(s): Magdalena Paczkowska, Przemyslaw Zalewski, Anna Krause, Magdalena Mroczkowska, Natalia Gozdz and Judyta Cielecka-Piontek

Volume 13, Issue 2, 2017

Page: [123 - 130] Pages: 8

DOI: 10.2174/1573412912666160927112436

Price: $65

Abstract

Background: A rapid stability-indicating UHPLC-DAD method was developed and validated for the determination of rutin in a bulk drug and diet supplements in the presence of related substances (impurities, degradation products, other active substances and excipients).

Experiment: A Kinetex C-18 (100 mm × 2.10 mm, 1.7 µm) column with semi-porous filling and the following separation conditions were used: mobile phase, acetonitrile–0.1% formic acid (20:80 V/V); flow rate, 0.4 mL/min; detection wavelength, 353 nm; column temperature, 298 K. The UHPLC-DAD method was linear in the range 0.20–1.40 µg with the correlation coefficients 0.9993 (rutin), 0.9995 (isoquercetin) and 0.9991 (quercetin), where accuracy and precision (intra- and inter-day) were acceptable. The limits of detection were 0.0436 µg (rutin), 0.0393 µg (isoquercetin) and 0.0442 µg (quercetin) whereas the limits of quantification were 0.1322 µg (rutin), 0.1192 µg (isoquercetin) and 0.1339 µg (quercetin).

Conclusion: The determination of rutin in the presence of its degradation products by using the UHPLCDAD method forming in aqueous solutions during acidic-basic hydrolysis and oxidation as well as in solid state during photolysis and thermolysis were studied. The degradation of rutin was a first-order reaction depending on the substrate concentration.

Keywords: Rutin, isoquercetin, quercetin, UHPLC-DAD, diet supplement, stability.

Graphical Abstract

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy