Optimization of several flavonoids separation by TLC

Authors

  • Natalia A. Belanova the senior engineer department of Analytical Chemistry, Voronezh State University, Voronezh, e-mail: belanovana@mail.ru
  • Sergey I. Karpov the senior lecturer of department of Analytical Chemistry, Voronezh State University, Voronezh, e-mail: karsiv@mail.ru
  • Vladimir F. Selemenev the professor, head of the department of Analytical Chemistry, Voronezh State University, Voronezh, e-mail: common@chem.vsu.ru
  • Ekaterina O. Shepeleva student of chemical faculty, Voronezh, Voronezh State University
  • Natalya V. Drozdova leading expert, FDCS of Russian federation Department in Voronezh Region, Voronezh
  • Yuri P. Afinogenov Prof., PhD, Depertment of Inorganic Chemistry Faculty of Chemistry. Voronezh, Voronezh State University

Keywords:

TLC, flavonoids, ( )-catechin, quercetin, rutin, naringin.

Abstract

Thin-layer chromatography retention parameters are defined for several flavonoids (rutin,
naringin, (+)-catechin, quercetin) in systems based on amylol and ethyl acetate as the elution system. The
change in the chromatographic parameters of flavonoids is considered, depending on the polarity of the
eluent by Snyder, Hildebrand parameter, the dielectric constant of solvents. The nonmonotonic variation
of the flavonoids retention demonstrates necessity to consider not only the polarity of the mobile phase,
but also the nature of the solvent that affects the interaction of flavonoids with the stationary phase.
Composition of the solvent system does not significantly affect on the retention of aglycones of
flavonoids (quercetin and (+)-catechin) if normal silica uses as a stationary phase. Replacement of the
stationary phase for polyamide leads to an inversion of the order of mass transfer for glicosidic for and
aglycones

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Published

2019-11-27

How to Cite

Optimization of several flavonoids separation by TLC. (2019). Sorbtsionnye I Khromatograficheskie Protsessy, 11(6). https://journals.vsu.ru/sorpchrom/article/view/2009

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