Physicochemical characteristics and in vitro permeation of loratadine solid lipid nanoparticles for transdermal delivery

Ther Deliv. 2020 Nov;11(11):685-700. doi: 10.4155/tde-2020-0075. Epub 2020 Nov 23.

Abstract

Aim: To prepare loratadine-loaded solid lipid nanoparticles (SLNs) using a modified two-step ultrasound-assisted phase inversion temperature (PIT) process. Results/methodology: Loratadine was dissolved in beeswax and Tween 80 was dissolved in water. The two phases were mixed together to prepare a water-in-oil emulsion preconcentrate (w/o) at a PIT of 85°C, followed by gradual water addition at 25°C to trigger nanoparticles formation (o/w). Kinetic stability was investigated. No change in the size was observed within 6 months. Fourier-transform infrared spectroscopy demonstrated stability of the emulsions via molecular structure of water at the interface of the o/w nanoemulsions. SLNs enhanced the in vitro skin permeation of loratadine. Conclusion: Stable SLNs were successfully prepared by ultrasound-assisted PIT.

Keywords: Franz diffusion cell; permeation; phase inversion temperature; pig skin; solid lipid nanoparticles; synthetic membrane; transdermal.

MeSH terms

  • Administration, Cutaneous
  • Emulsions
  • Lipids
  • Loratadine*
  • Nanoparticles*
  • Particle Size

Substances

  • Emulsions
  • Lipids
  • Loratadine