Nanoparticle-Mediated Systemic Delivery of siRNA for Treatment of Cancers and Viral Infections

被引:185
作者
Draz, Mohamed Shehata [1 ,2 ]
Fang, Binbin Amanda [3 ,4 ]
Zhang, Pengfei [5 ]
Hu, Zhi [6 ]
Gu, Shenda [6 ]
Weng, Kevin C.
Gray, Joe W. [4 ,6 ]
Chen, Fanqing Frank [1 ,3 ,4 ]
机构
[1] Zhejiang Univ, Zhejiang Calif Int Nanosyst Inst, Hangzhou 310029, Zhejiang, Peoples R China
[2] Tanta Univ, Fac Sci, Tanta 31527, Egypt
[3] Fudan Univ, Life Sci Coll, Shanghai 200433, Peoples R China
[4] Lawrence Berkeley Natl Lab, Div Life Sci, Berkeley, CA 94127 USA
[5] Second Mil Med Univ, Changzheng Hosp, Translat Med Ctr, Shanghai 200433, Peoples R China
[6] Oregon Hlth & Sci Univ, Ctr Spatial Syst Biomed, Portland, OR 97239 USA
关键词
Small interfering RNA; Nanoparticle; RNA interference; Delivery; Cancer; Virus; SMALL INTERFERING RNA; MESOPOROUS SILICA NANOPARTICLES; OVERCOME DRUG-RESISTANCE; DOUBLE-STRANDED-RNA; IN-VIVO DELIVERY; INTRACELLULAR DELIVERY; CARBON NANOTUBES; GOLD NANOPARTICLES; TARGETED DELIVERY; GENE DELIVERY;
D O I
10.7150/thno.9404
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
RNA interference (RNAi) is an endogenous post-transcriptional gene regulatory mechanism, where non-coding, double-stranded RNA molecules interfere with the expression of certain genes in order to silence it. Since its discovery, this phenomenon has evolved as powerful technology to diagnose and treat diseases at cellular and molecular levels. With a lot of attention, short interfering RNA (siRNA) therapeutics has brought a great hope for treatment of various undruggable diseases, including genetic diseases, cancer, and resistant viral infections. However, the challenge of their systemic delivery and on how they are integrated to exhibit the desired properties and functions remains a key bottleneck for realizing its full potential. Nanoparticles are currently well known to exhibit a number of unique properties that could be strategically tailored into new advanced siRNA delivery systems. This review summarizes the various nanoparticulate systems developed so far in the literature for systemic delivery of siRNA, which include silica and silicon-based nanoparticles, metal and metal oxides nanoparticles, carbon nanotubes, graphene, dendrimers, polymers, cyclodextrins, lipids, hydrogels, and semiconductor nanocrystals. Challenges and barriers to the delivery of siRNA and the role of different nanoparticles to surmount these challenges are also included in the review.
引用
收藏
页码:872 / 892
页数:21
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