Novel solid lipid nanoparticles as carriers for oral administration of insulin

Pharmazie. 2009 Sep;64(9):574-8.

Abstract

The aim of this study was to propose novel solid lipid nanoparticles (SLNs) loaded with cell-penetrating peptide (CPP), and to evaluate their potential for oral administration of insulin. Octaarginine (R8) was used as the CPP. SLNs loaded with insulin and R8 (Ra-Ins-SLNs) were prepared using the spontaneous emulsion solvent diffusion method. The morphological study of R8-Ins-SLNs showed its spherical shape using transmission electron microscopy (TEM) photography. The mean particle size, zeta potential, encapsulation efficiency (EE %) of insulin and R8 were 150.8 +/- 23.4 nm, 32.65 +/- 2.02 mV, 62.29 +/- 0.52% and 58.05 +/- 0.66%, respectively. The in vitro release of insulin or R8 from R8-Ins-SLNs was characterized by an initial rapid release and subsequent sustained release in pH 6.8 dissolution media. In vivo absorption experiments provided a relative pharmacological bioavailability (PA%) value of R8-Ins-SLN of 10.39 +/- 0.46%. These results suggest that SLNs loaded with CPP could be a promising perioral carrier for insulin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chemistry, Pharmaceutical
  • Drug Carriers*
  • Drug Compounding
  • Electrochemistry
  • Emulsions
  • Hypoglycemic Agents / administration & dosage*
  • Insulin / administration & dosage*
  • Intestinal Absorption
  • Liposomes
  • Male
  • Microscopy, Electron, Transmission
  • Nanoparticles*
  • Particle Size
  • Rats
  • Rats, Sprague-Dawley
  • Solubility

Substances

  • Drug Carriers
  • Emulsions
  • Hypoglycemic Agents
  • Insulin
  • Liposomes