A Serum-Resistant Cytofectin for Cellular Delivery of Antisense Oligodeoxynucleotides and Plasmid DNA

Development of antisense technology has focused in part on creating improved methods for delivering oligodeoxynucleotides (ODNs) to cells. In this report, we describe a cationic lipid that, when formulated with the fusogenic lipid dioleoylphosphatidylethanolamine, greatly improves the cellular uptak...

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Published in:Proceedings of the National Academy of Sciences - PNAS Vol. 93; no. 8; pp. 3176 - 3181
Main Authors: Lewis, Jason G., Lin, Kuei-Ying, Kothavale, Avinash, Flanagan, W. Michael, Matteucci, Mark D., DePrince, Randolph B., Mook, Robert A., Hendren, R. Wayne, Wagner, Richard W.
Format: Journal Article
Language:English
Published: United States National Academy of Sciences of the United States of America 16-04-1996
National Acad Sciences
National Academy of Sciences
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Summary:Development of antisense technology has focused in part on creating improved methods for delivering oligodeoxynucleotides (ODNs) to cells. In this report, we describe a cationic lipid that, when formulated with the fusogenic lipid dioleoylphosphatidylethanolamine, greatly improves the cellular uptake properties of antisense ODNs, as well as plasmid DNA. This lipid formulation, termed GS 2888 cytofectin, (i) efficiently transfects ODNs and plasmids into many cell types in the presence or absence of 10% serum in the medium, (ii) uses a 4- to 10-fold lower concentration of the agent as compared to the commercially available Lipofectin liposome, and (iii) is ≥ 20-fold more effective at eliciting antisense effects in the presence of serum when compared to Lipofectin. Here we show antisense effects using GS 2888 cytofectin together with C-5 propynyl pyrimidine phosphorothioate ODNs in which we achieve inhibition of gene expression using low nanomolar concentrations of ODN. This agent expands the utility of antisense ODNs for their use in understanding gene function and offers the potential for its use in DNA delivery applications in vivo.
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ISSN:0027-8424
1091-6490
DOI:10.1073/pnas.93.8.3176