Liposomal carfilzomib nanoparticles effectively target multiple myeloma cells and demonstrate enhanced efficacy in vivo.

Abstract

Carfilzomib, a recently FDA-approved proteasome inhibitor, has remarkable anti-myeloma (MM) activity. However, its effectiveness is limited by associated severe side-effects, short circulation half-life, and limited solubility. Here, we report the engineering of liposomal carfilzomib nanoparticles to overcome these problems and enhance the therapeutic efficacy of carfilzomib by increasing tumoral drug accumulation while decreasing systemic toxicity. In our design, carfilzomib was loaded into the bilayer of liposomes to yield stable and reproducible liposomal nanoparticles. Liposomal carfilzomib nanoparticles were efficiently taken up by MM cells, demonstrated proteasome inhibition, induced apoptosis, and exhibited enhanced cytotoxicity against MM cells. In vivo, liposomal carfilzomib demonstrated significant tumor growth inhibition and dramatically reduced overall systemic toxicity compared to free carfilzomib. Finally, liposomal carfilzomib demonstrated enhanced synergy in combination with doxorubicin. Taken together, this study establishes the successful synthesis of liposomal carfilzomib nanoparticles that demonstrates improved therapeutic index and the potential to improve patient outcome in MM.

• Authors: Jonathan D Ashley, Jared F Stefanick, Valerie A Schroeder, Mark A Suckow, Nathan J Alves, Rikio Suzuki, Shohei Kikuchi, Teru Hideshima, Kenneth C Anderson, Tanyel Kiziltepe, Basar Bilgicer
• Journal: Journal of controlled release : official journal of the Controlled Release Society (J Control Release) Vol. 196 Pg. 113-21 (Dec 28 2014) ISSN: 1873-4995 [Electronic] Netherlands
• PMID: 25312543 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2014 Elsevier B.V. All rights reserved.

Chemical References

• Antibiotics, Antineoplastic
• Antineoplastic Agents
• Integrin alpha4beta1
• Integrins
• Liposomes
• Oligopeptides
• Protease Inhibitors
• carfilzomib
• Doxorubicin

Topics

• Animals
• Antibiotics, Antineoplastic (pharmacology)
• Antineoplastic Agents (administration & dosage, pharmacology)
• Cell Line, Tumor
• Doxorubicin (pharmacology)
• Drug Synergism
• Humans
• Integrin alpha4beta1 (drug effects)
• Integrins (biosynthesis)
• Liposomes (chemistry)
• Mice
• Mice, SCID
• Multiple Myeloma (drug therapy)
• Nanoparticles
• Oligopeptides (administration & dosage, pharmacology)
• Particle Size
• Protease Inhibitors (administration & dosage, pharmacology)
• Solubility
• Xenograft Model Antitumor Assays