On Complex Formation between 5-Fluorouracil and β-Cyclodextrin in Solution and in the Solid State: IR Markers and Detection of Short-Lived Complexes by Diffusion NMR

Molecules. 2020 Dec 3;25(23):5706. doi: 10.3390/molecules25235706.

Abstract

In this work, the nuclear magnetic resonance (NMR) and IR spectroscopic markers of the complexation between 5-fluorouracil (5-FU) and β-cyclodextrin (β-CD) in solid state and in aqueous solution are investigated. In the attenuated total reflectance(ATR) spectra of 5-FU/β-CD products obtained by physical mixing, kneading and co-precipitation, we have identified the two most promising marker bands that could be used to detect complex formations: the C=O and C-F stretching bands of 5-FU that experience a blue shift by ca. 8 and 2 cm-1 upon complexation. The aqueous solutions were studied by NMR spectroscopy. As routine NMR spectra did not show any signs of complexation, we have analyzed the diffusion attenuation of spin-echo signals and the dependence of the population factor of slowly diffusing components on the diffusion time (diffusion NMR of pulsed-field gradient (PFG) NMR). The analysis has revealed that, at each moment, ~60% of 5-FU molecules form a complex with β-CD and its lifetime is ca. 13.5 ms. It is likely to be an inclusion complex, judging from the independence of the diffusion coefficient of β-CD on complexation. The obtained results could be important for future attempts of finding better methods of targeted anticancer drug delivery.

Keywords: 5-FU; IR; NMR; inclusion complex; molecular modeling; β-CD.

MeSH terms

  • Antineoplastic Agents / chemistry
  • Diffusion
  • Drug Delivery Systems / methods
  • Fluorouracil / chemistry*
  • Magnetic Resonance Spectroscopy / methods
  • Solubility
  • beta-Cyclodextrins / chemistry*

Substances

  • Antineoplastic Agents
  • beta-Cyclodextrins
  • Fluorouracil