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.
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