Ultra-pH-Responsive and Tumor-Penetrating Nanoplatform for Targeted siRNA Delivery with Robust Anti-Cancer Efficacy

被引:224
|
作者
Xu, Xiaoding [1 ]
Wu, Jun [1 ]
Liu, Yanlan [1 ]
Yu, Mikyung [1 ]
Zhao, Lili [1 ]
Zhu, Xi [1 ]
Bhasin, Sushant [1 ]
Li, Qing [1 ]
Ha, Emily [1 ]
Shi, Jinjun [1 ]
Farokhzad, Omid C. [1 ,2 ]
机构
[1] Harvard Med Sch, Brigham & Womens Hosp, Dept Anesthesiol, Boston, MA 02115 USA
[2] King Abdulaziz Univ, Jeddah, Saudi Arabia
基金
新加坡国家研究基金会;
关键词
cancer therapy; nanoparticles; pH-responsive; siRNA delivery; tumor penetration; NONVIRAL VECTORS; DRUG-DELIVERY; NANOPARTICLES; THERAPY;
D O I
10.1002/anie.201601273
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
RNA interference (RNAi) gene silencing technologies have shown significant potential for treating various diseases, including cancer. However, clinical success in cancer therapy remains elusive, mainly owing to suboptimal in vivo delivery of RNAi therapeutics such as small interference RNA (siRNA) to tumors. Herein, we developed a library of polymers that respond to a narrow pH change (ultra-pH-responsive), and demonstrated the utility of these materials in targeted and deep tumor-penetrating nanoparticle (NP) for in vivo RNAi. The new NP platform is mainly composed of the following key components: i) internalizing RGD (iRGD) to enhance tumor targeting and tissue penetration; ii) polyethylene glycol (PEG) chains to prolong blood circulation; and iii) sharp pH-responsive hydrophobic polymer to improve endosome escape. Through systematic studies of structure-function relationship, the optimized RNAi NPs (<70 nm) showed efficient gene silencing and significant inhibition of tumor growth with negligible toxicities in vivo.
引用
收藏
页码:7091 / 7094
页数:4
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