Multivesicular liposome formulations for the sustained delivery of interferon alpha-2b

Acta Pharmacol Sin. 2005 Nov;26(11):1395-401. doi: 10.1111/j.1745-7254.2005.00188.x.

Abstract

Aim: To develop and optimize a sustained release multivesicular liposome (MVL) formulation of interferon (IFN) alpha-2b.

Methods: IFN alpha-2b MVL were prepared using a typical double-emulsion procedure. The sustained release effects of IFN alpha-2b MVL were investigated by monitoring the blood IFN alpha-2b concentration using an enzyme-linked immunosorbent assay test after subcutaneous administration to healthy mice.

Results: IFN alpha-2b was successfully encapsulated in MVL with high efficiency, and the integrity of encapsulated protein was maintained. After subcutaneous injection, the MVL slowly released IFN alpha-2b into systemic circulation in a sustained manner. The estimated serum half-life of IFN alpha-2b was approximately 30 h. In addition, varying the size of the MVL preparations could further modify the in vivo release profile.

Conclusion: IFN alpha-2b MVL may be a useful sustained release formulation in the clinical treatment of viral diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antiviral Agents / administration & dosage*
  • Antiviral Agents / blood
  • Antiviral Agents / chemistry
  • Delayed-Action Preparations
  • Drug Compounding / methods*
  • Drug Delivery Systems
  • Female
  • Half-Life
  • Injections, Subcutaneous
  • Interferon alpha-2
  • Interferon-alpha / administration & dosage*
  • Interferon-alpha / blood
  • Interferon-alpha / chemistry
  • Liposomes*
  • Particle Size
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins

Substances

  • Antiviral Agents
  • Delayed-Action Preparations
  • Interferon alpha-2
  • Interferon-alpha
  • Liposomes
  • Recombinant Proteins