Targeted multifunctional gold-based nanoshells for magnetic resonance-guided laser ablation of head and neck cancer

被引:113
作者
Melancon, Marites P. [1 ,2 ]
Lu, Wei [2 ]
Zhong, Meng [2 ]
Zhou, Min [2 ]
Liang, Gan [4 ]
Elliott, Andrew M. [1 ]
Hazle, John D. [1 ]
Myers, Jeffrey N. [3 ]
Li, Chun [1 ]
Stafford, R. Jason [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Imaging Phys, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Expt Diagnost Imaging, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Head & Neck Surg, Houston, TX 77030 USA
[4] Sam Houston State Univ, Dept Phys, Huntsville, TX 77341 USA
基金
美国国家卫生研究院;
关键词
Theranostics; Gold nanoshells; Magnetic resonance imaging; Laser ablation; Ultrasmall paramagnetic iron oxide (SPIO); GROWTH-FACTOR RECEPTOR; PHOTOTHERMAL THERAPY; THERMAL THERAPY; ANTIBODY; NANOPARTICLES;
D O I
10.1016/j.biomaterials.2011.06.039
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Image-guided thermal ablation of tumors is becoming a more widely accepted minimally invasive alternative to surgery for patients who are not good surgical candidates, such as patients with advanced head and neck cancer. In this study, multifunctional superparamagnetic iron oxide coated with gold nanoshell (SPIO@Au NS) that have both optical and magnetic properties was conjugated with the targeting agent, C225 monoclonal antibody, against epidermal growth factor receptor (EGFR). C225-SPIO@Au NS have an average a diameter of 82 +/- 4.4 nm, contain 142 +/- 15 antibodies per nanoshell, have an absorption peak in the near infrared (similar to 800 nm), and have transverse relaxivity (r(2)) of 193 and 353 mM(-1) s(-1) versus Feridex (TM) of 171 and 300 mM(-1) s(-1), using 1.5 T and 71 MR scanners, respectively. Specific targeting of the synthesized C225-SPIO@Au NS was tested in vitro using A431 cells and oral cancer cells, FaDu, OSC19, and HN5, all of which overexpress EGFR. Selective binding was achieved using C225-SPIO@Au NS but not with the non-targeting PEG-SPIO@Au NS and blocking group (excess of C225 + C225-SPIO@Au NS). In vivo biodistribution on mice bearing A431 tumors also showed selective targeting of C225-SPIO@Au NS compared with the non-targeting and blocking groups. The selective photothermal ablation of the nanoshells shows that without laser treatment there were no cell death and among the groups that were treated with laser at a power of 36 W/cm(2) for 3 min, only the cells treated with C225-SPIO@Au NS had cell killing (p < 0.001). In summary, successful synthesis and characterization of targeted C225-SPIO@Au NS demonstrating both superparamagnetic and optical properties has been achieved. We have shown both in vitro and in vivo that these nanoshells are MR-active and can be selectively heated up for simultaneous imaging and photothermal ablation therapy. Published by Elsevier Ltd.
引用
收藏
页码:7600 / 7608
页数:9
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