Cholecalciferol complexation with hydroxypropyl-β-cyclodextrin (HPBCD) and its molecular dynamics simulation

Pharm Dev Technol. 2022 Apr;27(4):389-398. doi: 10.1080/10837450.2022.2064492. Epub 2022 Apr 25.

Abstract

The focus of the current study is to investigate cholecalciferol (vitamin D3) solubilization by hydroxypropyl-β-cyclodextrin (HPBCD) complexation through experimental and computational studies. Phase solubility diagram of vitamin D3 (completely insoluble in water) has an AP profile revealing a deviation from a linear regression with HPBCD concentration increase. Differential scanning calorimetry (DSC) is the best tool to confirm complex formation by disappearance of cholecalciferol exothermic peak in cholecalciferol-HPBCD complex thermogram, due to its amorphous state by entering HPBCD inner hydrophobic cavity, similarly validated by Fourier-transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). AP solubility diagram profile can be associated with cholecalciferol-HPBCD complex instability in liquid phase requiring spray drying to bring it to a solid dispersion state (always more stable) illustrated by scanning electron microscopy (SEM). Computational studies led to a deeper understanding and clarification, at molecular level, of the interactions within cholecalciferol-HPBCD complex. Thermodynamics and geometry of the complex were investigated by molecular dynamics (MD) simulation.

Keywords: Cholecalciferol (vitamin D3); complex; hydroxypropyl-β-cyclodextrin (HPBCD); molecular dynamic (MD) simulations; molecular modeling.

MeSH terms

  • 2-Hydroxypropyl-beta-cyclodextrin / chemistry
  • Calorimetry, Differential Scanning
  • Cholecalciferol
  • Molecular Dynamics Simulation*
  • Solubility
  • Spectroscopy, Fourier Transform Infrared / methods
  • X-Ray Diffraction
  • beta-Cyclodextrins* / chemistry

Substances

  • beta-Cyclodextrins
  • Cholecalciferol
  • 2-Hydroxypropyl-beta-cyclodextrin