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• W2050858308 abstract "Previous studies have examined different strategies for siRNA delivery with varying degrees of success. These include use of viral vectors, cationic liposomes, and polymers. Several copolymers were designed and synthesized based on blocks of poly(ethylene glycol) PEG, poly(propylene glycol) PPG, and poly(l-lysine). These were designated as P1, P2, and P3. We studied the copolymer self-assembly, siRNA binding, particle size, surface potential, architecture of the complexes, and siRNA delivery. Silencing of GFP using copolymer P3 to deliver GFP-specific siRNA to Neuro-2a cells expressing GFP was almost as effective as using Lipofectamine 2000, with minimal cytotoxicity. Thus, we have provided a new copolymer platform for siRNA delivery that we can continue to modify for improved delivery of siRNA in vitro and eventually in vivo." @default.
• W2050858308 created "2016-06-24" @default.
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• W2050858308 date "2013-12-18" @default.
• W2050858308 modified "2023-10-14" @default.
• W2050858308 title "Addition of poly (propylene glycol) to multiblock copolymer to optimize siRNA delivery" @default.
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• W2050858308 doi "https://doi.org/10.4161/bioe.27339" @default.
• W2050858308 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4008463" @default.
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