Epirubicin loaded to pre-polymerized poly(butyl cyanoacrylate) nanoparticles: Preparation and in vitro evaluation in human lung adenocarcinoma cells

被引:26
|
作者
Yordanov, Georgi [1 ]
Evangelatov, Alexander [2 ]
Skrobanska, Ralica [2 ]
机构
[1] Sofia Univ St Kliment Ohridski, Fac Chem & Pharm, Sofia 1164, Bulgaria
[2] Sofia Univ St Kliment Ohridski, Fac Biol, Sofia 1164, Bulgaria
关键词
Epirubicin; Poly(butyl cyanoacrylate); Nanoparticles; Lung cancer; A549; Cytotoxicity; Drug uptake; SOLID LIPID NANOPARTICLES; PHASE-II TRIAL; MACROMOLECULAR THERAPEUTICS; 1ST-LINE CHEMOTHERAPY; TARGETED DELIVERY; DOSE EPIRUBICIN; DOXORUBICIN; CANCER; DRUG; TUMOR;
D O I
10.1016/j.colsurfb.2013.02.002
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
This article describes the preparation of epirubicin-loaded nanoparticles, prepared by loading of the drug in pre-polymerized poly(butyl cyanoacrylate) nanoparticles, their physicochemical characterization and in vitro evaluation on human lung adenocarcinoma (A549) cells. Nanoparticles were also coated in aqueous dispersions with two different non-ionic surfactants (Pluronic F68 and Polysorbate 80). All particles were spherical in shape, with monomodal size distributions. The zeta-potentials at pH 7.4 increased with augmentation of the particle drug content. The increased drug content was found to correlate with the initial concentration of the drug, used for the particle preparation. In vitro studies on A549 cells showed that the drug-loaded nanoparticles, as well as the combinations of free drug and empty nanoparticles, exhibited higher cytotoxicity than the free drug alone. The presence of surfactants also resulted in increased cytotoxicity. Fluorescent imaging of epirubicin internalization by the adenocarcinoma cells revealed that the free drug was predominantly localized in the cell nucleus, while a cytoplasmic localization was observed for the nanoparticle-bound drug formulations, suggesting the probability of nanoparticle endocytosis. Thus the hereby presented results could be useful for development of nanoparticle-based anthracycline formulations for treatment of lung adenocarcinoma. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 123
页数:9
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