Fabrication of cyclodextrins-procainamide supramolecular self-assembly: shape-shifting of nanosheet into microtubular structure

Carbohydr Polym. 2015 May 20:122:123-34. doi: 10.1016/j.carbpol.2015.01.005. Epub 2015 Jan 13.

Abstract

Encapsulation behavior of α- and β-cyclodextrins (α-CD, β-CD) with procainamide hydrochloride (PCA) has been investigated by absorption, fluorescence, time-resolved fluorescence, proton nuclear magnetic resonance spectroscopy, scanning electron microscope, Fourier transform-infrared spectroscopy, differential scanning calorimetry, and powder X-ray diffraction techniques. Spectral results revealed that PCA forms 1:2 drug-CD2 inclusion complexes with CDs. Novel supramolecular self-assemblies have been fabricated by inclusion complexation of PCA with α-CD/β-CD and characterized by transmission electron microscope and micro-Raman imaging. The obtained results from transmission electron microscope indicated that PCA/α-CD complex could form nano-sized particles. However, when the macrocyclic ring with six glucose units was switched into seven glucose units, the resultant PCA/β-CD complex could be self-assembled to micro-sized tubular structures. Shape-shifting of 2D nanosheet into 1D microtube by simple rolling mechanism was analyzed. Thermodynamic parameters of inclusion process were determined by Parameter Method 3 calculations.

Keywords: Cyclodextrins; Microtubular structure; Nanoparticle; Procainamide hydrochloride; Rolling mechanism; Self-assembly.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbohydrate Conformation
  • Hydrogen-Ion Concentration
  • Models, Molecular
  • Nanostructures / chemistry*
  • Nanotechnology / methods*
  • Procainamide / chemistry*
  • Solvents / chemistry
  • Water / chemistry
  • beta-Cyclodextrins / chemistry*

Substances

  • Solvents
  • beta-Cyclodextrins
  • Water
  • Procainamide