Effect of surfactants and drug load on physico-mechanical and dissolution properties of nanocrystalline tadalafil-loaded oral films

Eur J Pharm Sci. 2017 Nov 15:109:372-380. doi: 10.1016/j.ejps.2017.08.019. Epub 2017 Aug 18.

Abstract

The aim of the present work was to prepare tadalafil (TDF) nanocrystals-loaded oral polymeric films (OFs) and investigate the effect of hydrophilic surfactants and drug loads on the physico-mechanical and dissolution properties. The nanosuspensions of TDF were prepared by high shear homogenization. HPMC based placebo casting film gel was prepared and mixed with TDF nanosuspensions. Films were casted using an automated film applicator and dried at 60°C for 45min. Particle size (PS), polydispersity index (PDI), and zeta potential (ZP) of TDF nanosuspensions were measured in a Zetasizer. The films were characterized using SEM, AFM, DSC, TGA and PXRD. The mechanical properties and in vitro drug release were determined using standard methods. TDF existed in crystalline form and the particles remained in the nano-range in redispersed films. TDF nanocrystals were embedded in the polymeric matrix and the drug loaded films were rough on the surface. Mechanical properties of the films varied with changes in drug load and surfactant. Significant changes in the disintegration times were noticed in films containing surfactants compared to surfactant-free films. About 80% of the drug release was observed between 3 and 30min. TPGS showed better TDF release from the films at different drug loads.

Chemical compounds: Hydroxy propyl methyl cellulose (PubChem CID: 57503849); Glycerol (PubChem CID: 753); Pluronic F-68 (PubChem CID: 24751); Vitamin E TPGS (PubChem CID: 71406).

Keywords: HPMC; Nanocrystals; Oral films; Poloxamer; Surfactants; Tadalafil; Vitamin E TPGS.

MeSH terms

  • Administration, Oral
  • Drug Delivery Systems*
  • Drug Liberation
  • Glycerol / chemistry
  • Hypromellose Derivatives / chemistry
  • Microscopy, Electron, Scanning
  • Nanoparticles / chemistry*
  • Nanoparticles / ultrastructure
  • Phosphodiesterase 5 Inhibitors / chemistry*
  • Poloxamer / chemistry
  • Solubility
  • Stress, Mechanical
  • Surface-Active Agents / chemistry*
  • Tadalafil / chemistry*
  • Tensile Strength
  • Vitamin E / chemistry

Substances

  • Phosphodiesterase 5 Inhibitors
  • Surface-Active Agents
  • Poloxamer
  • Vitamin E
  • Hypromellose Derivatives
  • Tadalafil
  • tocophersolan
  • Glycerol