Efficacy of edelfosine lipid nanoparticles in breast cancer cells.

Abstract

Breast cancer is a heterogeneous group of neoplasms predominantly originating in the terminal duct lobular units. It represents the leading cause of cancer death in women and the survival frequencies for patients at advanced stages of the disease remain low. New treatment options need to be researched to improve these rates. The anti-tumor ether lipid edelfosine (ET) is the prototype of a novel generation of promising anticancer drugs. However, it presents several drawbacks for its use in cancer therapy, including gastrointestinal and hemolytic toxicity and low oral bioavailability. To overcome these obstacles, ET was encapsulated in Precirol ATO 5 lipid nanoparticles (ET-LN), and its anti-tumor potential was in vitro tested in breast cancer. The formulated ET-LN were more effective in inhibiting cell proliferation and notably decreased cell viability, showing that the cytotoxic effect of ET was considerably enhanced when ET was encapsulated. In addition, ET and ET-LN were able to promote cell cycle arrest at G1 phase. Moreover, although both treatments provoked an apoptotic effect in a time-dependent manner, such anti-tumor effects were noticeably improved with ET-LN treatment. Therefore, our results indicate that encapsulating ET in LN played an essential role in improving the efficacy of the drug.

• Authors: María Ángela Aznar, Beatriz Lasa-Saracíbar, Ander Estella-Hermoso de Mendoza, María José Blanco-Prieto
• Journal: International journal of pharmaceutics (Int J Pharm) Vol. 454 Issue 2 Pg. 720-6 (Oct 01 2013) ISSN: 1873-3476 [Electronic] Netherlands
• PMID: 23643510 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2013 Elsevier B.V. All rights reserved.

Chemical References

• Antineoplastic Agents
• Diglycerides
• Phospholipid Ethers
• Polysorbates
• edelfosine
• precirol

Topics

• Antineoplastic Agents (administration & dosage, chemistry)
• Apoptosis (drug effects)
• Breast Neoplasms (drug therapy)
• Cell Cycle (drug effects)
• Cell Survival (drug effects)
• Diglycerides (chemistry)
• Female
• Humans
• MCF-7 Cells
• Nanoparticles (administration & dosage, chemistry)
• Phospholipid Ethers (administration & dosage, chemistry)
• Polysorbates (chemistry)