Efficacy of edelfosine lipid nanoparticles in breast cancer cells.
Int J Pharm
; 454(2): 720-6, 2013 Oct 01.
Article
em En
| MEDLINE
| ID: mdl-23643510
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.
Palavras-chave
ALPs; Alkylphospholipids; B-LN; Breast cancer; EPR effect; ET; ET-LN; Edelfosine; IC(50); LN; Lipid nanoparticles; MCF7; MCL; PDI; PI; alkylphospholipids; blank (unloaded) nanoparticles; edelfosine; edelfosine-loaded lipid nanoparticles; enhanced permeability and retention effect; inhibitory concentration 50; lipid nanoparticles; mantle cell lymphoma; polydispersity index; propidium iodide
Texto completo:
1
Base de dados:
MEDLINE
Assunto principal:
Neoplasias da Mama
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Éteres Fosfolipídicos
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Nanopartículas
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Antineoplásicos
Idioma:
En
Ano de publicação:
2013
Tipo de documento:
Article