RNA干扰
基因沉默
体内
基因敲除
PEG比率
化学
聚乙二醇
内体
聚乙二醇化
癌症
癌症研究
小干扰RNA
核糖核酸
生物
医学
基因
生物化学
细胞
生物技术
内科学
财务
经济
作者
Xiaoding Xu,Jun Wu,Yanlan Liu,Mikyung Yu,Lili Zhao,Xi Zhu,Sushant Bhasin,Qing Li,Emily Ha,Jinjun Shi,Omid C. Farokhzad
标识
DOI:10.1002/anie.201601273
摘要
Abstract 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.
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