Synthesis and characterization of multifunctional Fe3O4/poly(fluorescein O-methacrylate) core/shell nanoparticles

被引:17
|
作者
Govindaiah, Patakamuri [2 ]
Hwang, Taewon [2 ]
Yoo, Hyunhee [2 ]
Kim, Yong Seok [2 ]
Lee, Sun Jong [2 ]
Choi, Sung Wook [1 ]
Kim, Jung Hyun [2 ]
机构
[1] Catholic Univ Korea, Dept Biotechnol, Bucheon Si 420743, Gyeonggi Do, South Korea
[2] Yonsei Univ, Dept Chem & Biomol Engn, Seoul 120749, South Korea
基金
新加坡国家研究基金会;
关键词
Core/shell; Fluorescent; Nanoparticles; Multifunctional; Superparamagnetic; Bioimaging; IRON-OXIDE NANOPARTICLES; FLUORESCENT; NANOSPHERES; TEMPERATURE; SEPARATION; PARTICLES; BEHAVIOR; THERAPY; POLYMER; DRUG;
D O I
10.1016/j.jcis.2012.04.055
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 fluorescent and superparamagnetic Fe3O4/poly(fluorescein O-methacrylate) [Fe3O4/poly (FMA)] nanoparticles with core/shell structure were synthesized via surface-initiated polymerization. First, polymerizable double bonds were introduced onto the surface of Fe3O4 nanoparticles via ligand exchange and a condensation reaction. A fluorescent monomer, FMA, was then polymerized to the double bonds at the surface via free-radical polymerization, leading to form a fluorescent polymer shell around the superparamagnetic Fe3O4 core. The resultant Fe3O4/poly(FmA) nanoparticles were characterized by Fourier transform infrared, nuclear magnetic resonance, and X-ray diffraction spectroscopy to confirm the reactions. Transmission electron microscopy images showed that the Fe3O4/poly(FMA) nanoparticles have a spherical and monodisperse core/shell morphology. Photoluminescence spectroscopy and superconducting quantum interference device magnetometer analyses confirmed that the Fe3O4/poly(FMA) nanoparticles exhibited fluorescent and superparamagnetic properties, respectively. In addition, we demonstrated the potential bioimaging application of the Fe3O4/poly(FMA) nanoparticles by visualizing the cellular uptake of the nanoparticles into A549 lung cancer cells. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:27 / 32
页数:6
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