Uniform Mesoporous Dye-Doped Silica Nanoparticles Decorated with Multiple Magnetite Nanocrystals for Simultaneous Enhanced Magnetic Resonance Imaging, Fluorescence Imaging, and Drug Delivery

被引:634
作者
Lee, Ji Eun [1 ,2 ]
Lee, Nohyun [1 ,2 ]
Kim, Hyoungsu [3 ,4 ]
Kim, Jaeyun [1 ,2 ]
Choi, Seung Hong [3 ,4 ]
Kim, Jeong Hyun [1 ,2 ]
Kim, Taeho [1 ,2 ]
Song, In Chan [3 ,4 ]
Park, Seung Pyo [1 ,2 ]
Moon, Woo Kyung [3 ,4 ]
Hyeon, Taeghwan [1 ,2 ]
机构
[1] Seoul Natl Univ, Natl Creat Res Initiat Ctr Oxide Nanocrystalline, Seoul 151744, South Korea
[2] Seoul Natl Univ, Sch Chem & Biol Engn, Seoul 151744, South Korea
[3] Seoul Natl Univ Hosp, Seoul 110744, South Korea
[4] Seoul Natl Univ, Med Res Ctr, Inst Radiat Med, Seoul 110744, South Korea
基金
新加坡国家研究基金会;
关键词
RESPONSIVE CONTROLLED-RELEASE; QUANTUM DOTS; CONTRAST AGENTS; INORGANIC NANOPARTICLES; DESIGNED FABRICATION; OXIDE NANOPARTICLES; SHELL; CORE; SYSTEM; CELLS;
D O I
10.1021/ja905793q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Highly versatile nanocomposite nanoparticles were synthesized by decorating the surface of mesoporous dye-doped silica nanoparticles with multiple magnetite nanocrystals. The superparamagnetic property of the magnetite nanocrystals enabled the nanoparticles to be used as a contrast agent in magnetic resonance (MR) imaging, and the dye molecule in the silica framework imparted optical imaging modality. Integrating a multitude of magnetite nanocrystals on the silica surface resulted in remarkable enhancement of MR signal due to the synergistic magnetism. An anticancer drug, doxorubicin (DOX), could be loaded in the pores and induced efficient cell death. In vivo passive targeting and accumulation of the nanoparticles at the tumor sites was confirmed by both T2 MR and fluorescence imaging. Furthermore, apoptotic morphology was clearly detected in tumor tissues of mice treated with DOX loaded nanocomposite nanoparticles, demonstrating that DOX was successfully delivered to the tumor sites and its anticancer activity was retained.
引用
收藏
页码:552 / 557
页数:6
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