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A fabricated siRNA nanoparticle for ultra-long gene silencing in vivo.


ABSTRACT: Persistent gene silencing is crucially required for the successful therapeutics of short interfering RNA (siRNA). Here, we describe a nanoparticle based delivery system which assembled by layering siRNAs between protease degradable polypeptides to extend the therapeutic window. These tightly packed nanoparticles are efficiently taken up by cells by endocytosis, and the fabricated siRNAs are gradually released following intracellular degradation of the polypeptide layers. During cell division, the particles are distributed to the daughter cells. Due to the slow degradation through the multiple layers, the particles continuously release siRNA in all cells. Using this controlled release construct, the in vivo gene silencing effect of siRNA is consistent for an ultra-long period of time (>3 weeks) with only a single treatment.

SUBMITTER: Lee SK 

PROVIDER: S-EPMC4078887 | biostudies-literature | 2013 Jul

REPOSITORIES: biostudies-literature

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A fabricated siRNA nanoparticle for ultra-long gene silencing <i>in vivo.</i>

Lee Seung Koo SK   Tung Ching-Hsuan CH  

Advanced functional materials 20130701 28


Persistent gene silencing is crucially required for the successful therapeutics of short interfering RNA (siRNA). Here, we describe a nanoparticle based delivery system which assembled by layering siRNAs between protease degradable polypeptides to extend the therapeutic window. These tightly packed nanoparticles are efficiently taken up by cells by endocytosis, and the fabricated siRNAs are gradually released following intracellular degradation of the polypeptide layers. During cell division, th  ...[more]

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