Multifunctional poly(aspartic acid) nanoparticles containing iron oxide nanocrystals and doxorubicin for simultaneous cancer diagnosis and therapy

被引:29
作者
Yang, Hee-Man [1 ]
Oh, Byung Chang [1 ]
Kim, Jong Hun [1 ]
Ahn, Taebin [1 ]
Nam, Ho-Seong [1 ]
Park, Chan Woo [1 ]
Kim, Jong-Duk [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, Grad Program BK21, Taejon 305701, South Korea
关键词
Poly(aspartic acid)s; Iron oxide nanocrystals; Doxorubicin; Magnetic resonance imaging; Cancer therapy; DRUG-DELIVERY; BREAST-CANCER; MAGNETIC NANOPARTICLES; CARRIER; DERIVATIVES; POLYMER;
D O I
10.1016/j.colsurfa.2011.04.032
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Multifunctional poly(aspartic acid) nanoparticles for simultaneous cancer diagnosis and therapy were developed. First, iron oxide nanocrystals were loaded in poly(aspartic acid) nanoparticles through an emulsion method using octadecyl grafted poly(aspartic acid). The influence of the organic solvent, used to disperse the hydrophobic iron oxide nanocrystals, on the size and loading efficiency of iron oxide nanocrystals loaded poly(aspartic acid) nanoparticles was investigated. Next, an anticancer drug, doxorubicin (DOX), was incorporated in the magnetic poly(aspartic acid) nanoparticles (MPAN). The presence of iron oxide nanocrystals in the poly(aspartic acid) nanoparticles and their size distribution were confirmed by transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), and dynamic light scattering (DLS), respectively. The drug release behavior was also observed for 3 days. From the results of T-2 weighted MR imaging and MTT assays, the DOX loaded MPAN showed high T-2 relaxivity coefficients and high cytotoxicity for cancer cells. Crown Copyright (C) 2011 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:208 / 215
页数:8
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