Investigation of the Membrane Localization and Interaction of Selected Flavonoids by NMR and FTIR Spectroscopy

Int J Mol Sci. 2023 Oct 17;24(20):15275. doi: 10.3390/ijms242015275.

Abstract

In this report, we discuss the effects of undescribed flavone derivatives, HZ4 and SP9, newly isolated from the aerial parts of Hottonia palustris L. and Scleranthus perennis L. on membranes. Interaction of flavonoids with lipid bilayers is important for medicinal applications. The experiments were performed with FTIR and NMR techniques on liposomes prepared from DPPC (dipalmitoylphosphatidylcholine) and EYPC (egg yolk phosphatidylcholine). The data showed that the examined polyphenols incorporate into the polar head group region of DPPC phospholipids at both 25 °C and 45 °C. At the lower temperature, a slight effect in the spectral region of the ester carbonyl group is observed. In contrast, at 45 °C, both compounds bring about the changes in the spectral regions attributed to antisymmetric and symmetric stretching vibrations of CH2 and CH3 moieties. Similarly, as in DPPC lipids, the tested compounds interact with the fingerprint region of the polar head groups of the EYPC lipids and cause its reorganization. The outcomes obtained by NMR analyses confirmed the localization of both flavonoids in the polar heads zone. Unraveled effects of HZ4 and SP9 in respect to lipid bilayers can partly determine their biological activities and are crucial for their usability in medicine as disease-preventing phytochemicals.

Keywords: DPPC; EYPC; FTIR; NMR; flavonoids; liposomes.

MeSH terms

  • 1,2-Dipalmitoylphosphatidylcholine / chemistry
  • Flavonoids*
  • Lipid Bilayers* / chemistry
  • Liposomes / chemistry
  • Magnetic Resonance Spectroscopy
  • Spectroscopy, Fourier Transform Infrared / methods

Substances

  • Lipid Bilayers
  • Flavonoids
  • Liposomes
  • 1,2-Dipalmitoylphosphatidylcholine