Colloidal formulations of etoposide based on poly(butyl cyanoacrylate) nanoparticles: Preparation, physicochemical properties and cytotoxicity

被引:34
|
作者
Yordanov, Georgi [1 ]
Skrobanska, Ralica [2 ]
Evangelatov, Alexander [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
Etoposide; Poly(butyl cyanoacrylate); Nanoparticles; Cancer; A549; Cytotoxicity; Apoptosis; SOLID LIPID NANOPARTICLES; DALTONS LYMPHOMA; DRUG-DELIVERY; IN-VITRO; POLYETHYLCYANOACRYLATE NANOPARTICLES; CLINICAL-PHARMACOLOGY; BUTYL CYANOACRYLATE; DOXORUBICIN; LIPOSOMES; RELEASE;
D O I
10.1016/j.colsurfb.2012.05.040
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
This article describes the preparation, physicochemical characterization and cytotoxicity assessment of novel colloidal formulations of etoposide based on poly(butyl cyanoacrylate) nanoparticles. Nanoparticles were prepared by controlled emulsion polymerization of butyl cyanoacrylate in aqueous medium using two different non-ionic colloidal stabilizers (pluronic F68 and polysorbate 80). The nanoparticles were spherical in shape, with average size ranging from 110-150 nm (empty nanoparticles) to 170-260 nm (drug-loaded nanoparticles), monomodal size distributions, and negative zeta-potentials at pH 7.4. Drug loading efficiency was around 63-68%. More than 80% of the drug was released from the formulations within 6-7 h of dialysis experiments. Pluronic-coated nanoparticles possessed lower magnitude of the zeta-potentials (around -4 mV) in comparison with the polysorbate-coated ones (around -12 mV). All tested etoposide formulations induced apoptosis in adenocarcinoma human epithelial (A549) cells, as evident from condensation of chromatin and fragmentation of nuclei. It was found that etoposide formulated with poly(butyl cyanoacrylate) nanoparticles and polysorbate 80 exhibited the highest cytotoxicity toward adenocarcinoma cells. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:215 / 222
页数:8
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