A fabricated siRNA nanoparticle for ultra-long gene silencing in vivo. Academic Article uri icon

Overview

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.

publication date

  • July 26, 2013

Identity

PubMed Central ID

  • PMC4078887

Scopus Document Identifier

  • 84880586844

Digital Object Identifier (DOI)

  • 10.1002/adfm.201202777

PubMed ID

  • 24999314

Additional Document Info

volume

  • 23

issue

  • 28