RNAi-mediated gene-targeting through systemic application of polyethylenimine (PEI)-complexed siRNA in vivo
By Beata Urban-Klein, S. Werth, Shaker Abuharbeid, F. Czubayko, A. Aigner. Gene Therapy, 2005
735 citations recorded by the source corpus.
Subfields: Molecular Biology, Polymers and Plastics
View Paper: https://www.semanticscholar.org/paper/f260e842ebfba0cd87de1a8f4e50fa60a27b3714
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In Molecular Biology
Citations in the corpus
- Breaking down the barriers: siRNA delivery and endosome escape (2010, background): “Polyethyleneimine (PEI) is one of the most widely used cationic polymers for nucleic acid delivery (Read et al., 2005; Richards Grayson et al., 2006; Urban-Klein et al., 2005).”
- Nanocarriers’ entry into the cell: relevance to drug delivery (2009, methodology): “In vivo, these polyplexes also displayed antitumoral activity after subcutaneous or intraperitoneal administration, as shown with a siRNA targeted against the growth factor pleiotrophin [185] and the HER-2 receptor [186] in murine subcutaneous tumor models.”
- Innovative approaches for cancer treatment: current perspectives and new challenges (2019, background): “PEI is able to form small cationic nanoparticles containing siRNAs and it has been exploited as antitumoural, upon loading with HER-2 receptor-specific siRNA [201].”
- siRNA delivery systems for cancer treatment. (2009, background): “PEI-complexed siRNA, but not free siRNA, resulted in a marked reduction in tumor growth through siRNAmediated HER-2 downregulation in the animal model [111].”
- RNAi therapeutics: a potential new class of pharmaceutical drugs (2006, background): “Simpler PEI formulations have also shown efficacy in xenograft tumor models 79 , as have complexes of siRNA duplexes with atelocollagen.”