| Literature DB >> 17676782 |
Mathieu Mével1, Tristan Montier, François Lamarche, Pascal Delépine, Tony Le Gall, Jean-Jacques Yaouanc, Paul-Alain Jaffrès, Dominique Cartier, Pierre Lehn, Jean-Claude Clément.
Abstract
Lipophosphoramidates with two different permanent cations as polar heads were synthesized and evaluated for their gene transfer activity. Physicochemical measurements (particle size, zeta potentials) and gel retardation assays were also performed. In vitro biological evaluation was conducted with A542 and HeLa cell lines, and cytotoxicity determined by a chemiluminescent assay. The set of results indicates that, on the whole, dicationic lipophosphoramidates constitute an interesting alternative to their monocationic analogues.Entities:
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Year: 2007 PMID: 17676782 DOI: 10.1021/bc070089z
Source DB: PubMed Journal: Bioconjug Chem ISSN: 1043-1802 Impact factor: 4.774