Engineered Zn(II)-Dipicolylamine-Gold Nanorod Provides Effective Prostate Cancer Treatment by Combining siRNA Delivery and Photothermal Therapy

被引:37
|
作者
Min, Kyung Hyun [1 ,2 ]
Kim, Young-Hwa [1 ]
Wang, Zhantong [1 ]
Kim, Jihoon [1 ]
Kim, Jee Seon [1 ]
Kim, Sun Hwa [2 ]
Kim, Kwangmeyung [2 ]
Kwon, Ick Chan [2 ]
Kiesewetter, Dale O. [1 ]
Chen, Xiaoyuan [1 ]
机构
[1] Natl Inst Biomed Imaging & Bioengn, Lab Mol Imaging & Nanomed, NIH, Bethesda, MD 20892 USA
[2] Korea Inst Sci & Technol, Biomed Res Inst, Ctr Theragnosis, Seoul 136791, South Korea
来源
THERANOSTICS | 2017年 / 7卷 / 17期
基金
美国国家卫生研究院; 新加坡国家研究基金会;
关键词
dipicolylamine; metal-organic complexes; siRNA; gold nanorod; photothermal therapy; photoacoustic imaging; combination therapy; theranostics; ADVANCED SOLID TUMORS; POLO-LIKE KINASE-1; PHASE-I; SYSTEMIC DELIVERY; PAMAM DENDRIMER; GENE DELIVERY; CELL-DIVISION; GOLD NANORODS; NANOPARTICLES; CYTOTOXICITY;
D O I
10.7150/thno.22435
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Combination cancer treatment has emerged as a critical approach to achieve remarkable anticancer effect. In this study, we prepared a theranostic nanoformulation that allows for photoacoustic imaging as well as combination gene and photothermal therapy. Gold nanorods (GNR) were coated with dipicolyl amine (DPA), which forms stable complexes with Zn2+ cations. The resulting nanoparticles, Zn(II)/DPA-GNR, recognize phosphate-containing molecules, including siRNA, because of the specific interaction between Zn(II) and the phosphates. We chose anti-polo-like kinase 1 siRNA (siPLK) as our example for gene silencing. The strong complexation between Zn(II)/DPA-GNR and siPLK provided high stability to the nano-complexes, which efficiently delivered siRNA into the targeted cancer cells in vitro and in vivo. The particle served as a theranostic agent because the GNRs of nano-complexes permitted effective photothermal therapy as well as photoacoustic imaging upon laser irradiation. This gene/photothermal combination therapy using siPLK/Zn(II) DPA-GNRs exhibited significant antitumor activity in a PC-3 tumor mouse model. The concept described in this work may be extended to the development of efficient delivery strategies for other polynucleotides as well as advanced anticancer therapy.
引用
收藏
页码:4240 / 4254
页数:15
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