Bortezomib-loaded lipidic-nano drug delivery systems; formulation, therapeutic efficacy, and pharmacokinetics

J Microencapsul. 2021 May;38(3):192-202. doi: 10.1080/02652048.2021.1876175. Epub 2021 Feb 2.

Abstract

Aim: Nano drug delivery systems can provide the opportunity to reduce side effects and improve the therapeutic aspect of a variety of drugs. Bortezomib (BTZ) is a proteasome inhibitor approved for the treatment of multiple myeloma and mantle cell lymphoma. Severe side effects of BTZ are the major dose-limiting factor. Particulate drug delivery systems for BTZ are polymeric and lipidic drug delivery systems. This review focussed on lipidic-nano drug delivery systems (LNDDSs) for the delivery of BTZ.

Results: LNDDSs including liposomes, solid lipid nanoparticles, and self-nanoemulsifying drug delivery systems showed reduce systemic side effects, improved therapeutic efficacy, and increased intestinal absorption. Besides LNDDSs were used to target-delivery of BTZ to cancer.

Conclusion: Overall, LNDDSs can be considered as a novel delivery system for BTZ to resolve the treatment-associated restrictions.

Keywords: Bortezomib; formulation; liposomes; pharmacokinetics; self-nanoemulsifying drug delivery systems; solid lipid nanoparticles.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / administration & dosage
  • Bortezomib / administration & dosage*
  • Bortezomib / pharmacokinetics
  • Bortezomib / therapeutic use
  • Drug Compounding
  • Drug Delivery Systems*
  • Emulsions
  • Humans
  • Lipids / chemistry*
  • Liposomes
  • Nanoparticles*
  • Particle Size
  • Proteasome Inhibitors / administration & dosage*
  • Proteasome Inhibitors / pharmacokinetics
  • Proteasome Inhibitors / therapeutic use
  • Rats

Substances

  • Antineoplastic Agents
  • Emulsions
  • Lipids
  • Liposomes
  • Proteasome Inhibitors
  • Bortezomib