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

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 trea...

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Autores principales: Draz, Mohamed Shehata, Fang, Binbin Amanda, Zhang, Pengfei, Hu, Zhi, Gu, Shenda, Weng, Kevin C., Gray, Joe W., Chen, Fanqing Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107289/
https://www.ncbi.nlm.nih.gov/pubmed/25057313
http://dx.doi.org/10.7150/thno.9404
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author Draz, Mohamed Shehata
Fang, Binbin Amanda
Zhang, Pengfei
Hu, Zhi
Gu, Shenda
Weng, Kevin C.
Gray, Joe W.
Chen, Fanqing Frank
author_facet Draz, Mohamed Shehata
Fang, Binbin Amanda
Zhang, Pengfei
Hu, Zhi
Gu, Shenda
Weng, Kevin C.
Gray, Joe W.
Chen, Fanqing Frank
author_sort Draz, Mohamed Shehata
collection PubMed
description 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.
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spelling pubmed-41072892014-07-23 Nanoparticle-Mediated Systemic Delivery of siRNA for Treatment of Cancers and Viral Infections Draz, Mohamed Shehata Fang, Binbin Amanda Zhang, Pengfei Hu, Zhi Gu, Shenda Weng, Kevin C. Gray, Joe W. Chen, Fanqing Frank Theranostics Review 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. Ivyspring International Publisher 2014-06-11 /pmc/articles/PMC4107289/ /pubmed/25057313 http://dx.doi.org/10.7150/thno.9404 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Review
Draz, Mohamed Shehata
Fang, Binbin Amanda
Zhang, Pengfei
Hu, Zhi
Gu, Shenda
Weng, Kevin C.
Gray, Joe W.
Chen, Fanqing Frank
Nanoparticle-Mediated Systemic Delivery of siRNA for Treatment of Cancers and Viral Infections
title Nanoparticle-Mediated Systemic Delivery of siRNA for Treatment of Cancers and Viral Infections
title_full Nanoparticle-Mediated Systemic Delivery of siRNA for Treatment of Cancers and Viral Infections
title_fullStr Nanoparticle-Mediated Systemic Delivery of siRNA for Treatment of Cancers and Viral Infections
title_full_unstemmed Nanoparticle-Mediated Systemic Delivery of siRNA for Treatment of Cancers and Viral Infections
title_short Nanoparticle-Mediated Systemic Delivery of siRNA for Treatment of Cancers and Viral Infections
title_sort nanoparticle-mediated systemic delivery of sirna for treatment of cancers and viral infections
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4107289/
https://www.ncbi.nlm.nih.gov/pubmed/25057313
http://dx.doi.org/10.7150/thno.9404
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