Application of Gold Nanorods for Plasmonic and Magnetic Imaging of Cancer Cells

被引:19
作者
Liu, Liwei [1 ,2 ,3 ]
Ding, Hong [1 ,2 ]
Yong, Ken-Tye [1 ,2 ]
Roy, Indrajit [1 ,2 ]
Law, Wing-Cheung [1 ,2 ]
Kopwitthaya, Atcha [2 ]
Kumar, Rajiv [2 ]
Erogbogbo, Folarin [2 ]
Zhang, Xihe [1 ,3 ]
Prasad, Paras N. [1 ,2 ]
机构
[1] Int Joint Res Ctr Nanophoton & Biophoton, Changchun 130022, Jilin, Peoples R China
[2] SUNY Buffalo, ILPB, Buffalo, NY 14260 USA
[3] Changchun Univ Sci & Technol, Sch Sci, Changchun 130022, Jilin, Peoples R China
关键词
Gold nanorods; Cancer; Dark-field imaging; MRI; DOTA; Gd; CONTRAST AGENTS; QUANTUM DOTS; SILICA NANOPARTICLES; RESONANCE; BIODISTRIBUTION; NANOTECHNOLOGY; THERAPY; SHAPE; SIZE;
D O I
10.1007/s11468-010-9175-2
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
We report the use of biocompatible gold nanorods (GNRs) as multimodal (plasmonic and magnetic) probes for cancer cell labeling in vitro. These multifunctional and multimodal bioconjugates were prepared by replacing cetyltrimethylammonium bromide with a mixture of functionalized PEGylation molecules so that a variety of functionalities (e.g., magnetic resonance imaging agent gadolinium (Gd) and biorecognition molecule transferrin (Tf)) can be easily integrated using simple chemistry. It was shown that Gd incorporation did not interfere with the plasmonic properties of the GNRs and a strong T1 relaxivity was estimated (10.0 mM(-1) s(-1)), which is more than twice that of the clinical MRI agent Gd-DTPA. The large observed T1 relaxivity was possibly due to the huge surface to volume ratio of GNR, which allowed huge amount of amine-terminated molecule to anchor on the surface, coupled with Gd (III) ions for the enhanced relaxation of water protons. Pancreatic cancer cell overexpressing the transferring receptor was served as the in vitro model, and the Tf-mediated uptake was demonstrated and confirmed by dark-field imaging and transmission electron microscopy. More importantly, cell viability (MTS) assay did not reveal any sign of toxicity in these treated cells, suggesting that PEGylated GNRs can serve as a biocompatible, multifunctional, and multimodal platform for variable bio-applications.
引用
收藏
页码:105 / 112
页数:8
相关论文
共 49 条
[41]  
SULLIVAN D, 2004, MOL IMAGING
[42]   A clearer vision for in vivo imaging [J].
Weissleder, R .
NATURE BIOTECHNOLOGY, 2001, 19 (04) :316-317
[43]   Nanoscience, nanotechnology, and chemistry [J].
Whitesides, GM .
SMALL, 2005, 1 (02) :172-179
[44]   Covalently Combining Carbon Nanotubes with Anticancer Agent: Preparation and Antitumor Activity [J].
Wu, Wei ;
Li, Rutian ;
Bian, Xiaochen ;
Zhu, Zhenshu ;
Ding, Dan ;
Li, Xiaolin ;
Jia, Zhijun ;
Jiang, Xiqun ;
Hu, Yiqiao .
ACS NANO, 2009, 3 (09) :2740-2750
[45]   Biocompatible Near-Infrared Quantum Dots as Ultrasensitive Probes for Long-Term in vivo Imaging Applications [J].
Yong, Ken-Tye ;
Roy, Indrajit ;
Ding, Hong ;
Bergey, Earl J. ;
Prasad, Paras N. .
SMALL, 2009, 5 (17) :1997-2004
[46]   Mn-doped near-infrared quantum dots as multimodal targeted probes for pancreatic cancer imaging [J].
Yong, Ken-Tye .
NANOTECHNOLOGY, 2009, 20 (01)
[47]   Preparation of Gold Nanoparticles and their Applications in Anisotropic Nanoparticle Synthesis and Bioimaging [J].
Yong, Ken-Tye ;
Swihart, Mark T. ;
Ding, Hong ;
Prasad, Paras N. .
PLASMONICS, 2009, 4 (02) :79-93
[48]   Quantitative CT Imaging of the Spatial and Temporal Distribution of Liposomes in a Rabbit Tumor Model [J].
Zheng, Jinzi ;
Jaffray, David ;
Allien, Christine .
MOLECULAR PHARMACEUTICS, 2009, 6 (02) :571-580
[49]   Additive controlled synthesis of gold nanorods (GNRs) for two-photon luminescence imaging of cancer cells [J].
Zhu, Jing ;
Yong, Ken-Tye ;
Roy, Indrajit ;
Hu, Rui ;
Ding, Hong ;
Zhao, Lingling ;
Swihart, Mark T. ;
He, Guang S. ;
Cui, Yiping ;
Prasad, Paras N. .
NANOTECHNOLOGY, 2010, 21 (28)