| Literature DB >> 27140428 |
Xiaoding Xu1, Jun Wu1, Yanlan Liu1, Mikyung Yu1, Lili Zhao1, Xi Zhu1, Sushant Bhasin1, Qing Li1, Emily Ha1, Jinjun Shi1, Omid C Farokhzad1,2.
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.Entities:
Keywords: cancer therapy; nanoparticles; pH-responsive; siRNA delivery; tumor penetration
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Year: 2016 PMID: 27140428 PMCID: PMC4972612 DOI: 10.1002/anie.201601273
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336