| Literature DB >> 19159294 |
Claire Ceballos1, Carla A H Prata, Suzanne Giorgio, Frédéric Garzino, Dominique Payet, Philippe Barthélémy, Mark W Grinstaff, Michel Camplo.
Abstract
Cationic nucleoside lipids based on a 3-nitropyrrole universal base were prepared from D-ribose using a straightforward chemical synthesis. Several studies including DLS, TEM, and ethidium bromide (EthBr) assay demonstrated that these amphiphilic molecules form supramolecular organizations of nanometer size in aqueous solutions and are able to bind nucleic acids. siRNA knockdown experiments were performed with these nucleolipids, and we observed protein knockdown activity similar to the siPORT NeoFX positive control. No significant cytotoxicity was found.Entities:
Mesh:
Substances:
Year: 2009 PMID: 19159294 PMCID: PMC2819530 DOI: 10.1021/bc800432n
Source DB: PubMed Journal: Bioconjug Chem ISSN: 1043-1802 Impact factor: 4.774