Anionic liposomal delivery system for DNA transfection

Journal Title: The AAPS Journal - Year 2004, Vol 6, Issue 4

Abstract

The present study investigates the use of novel anionic lipoplexes composed of physiological components for plasmid DNA delivery into mammalian cells in vitro. Liposomes were prepared from mixtures of endogenously occurring anionic and zwitterionic lipids, 1,2-dioleoyl-sn-glycero-3-[phospho-rac-(1-glycerol)] (sodium salt) (DOPG) and 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE), respectively, at a molar ratio of 17∶83 (DOPG:DOPE). Anionic lipoplexes were formed by complexation between anionic liposomes and plasmid DNA molecules encoding green fluorescence protein (GFP) using Ca2+ ions. Transfection and toxicity were evaluated in CHO-K1 cells using flow cytometry and propidium iodide staining, respectively. Controls included Ca2+-DNA complexes (without lipids), anionic liposomes (no Ca2+), and a cationic liposomal formulation. Efficient delivery of plasmid DNA and subsequent GFP expression was achieved using anionic lipoplexes. Transfection efficiency increased with Ca2+ concentration up to 14 mM Ca2+, where transfection efficiency was 7-fold higher than in untreated cells, with minimum toxicity. Further increase in Ca2+ decreased transfection. Transfection efficiency of anionic lipoplexes was similar to that of cationic liposomes (lipofect Amine), whereas their toxicity was significantly lower. Ca2+-DNA complexes exhibited minimal and irregular transfection with relatively high cytotoxicity. A model was developed to explain the basis of anionic lipoplex uptake and transfection efficacy. Effective transfection is explained on the formation of nonbilayer hexagonal lipid phases. Efficient and relatively safe DNA transfection using anionic lipoplexes makes them an appealing alternative to be explored for gene delivery.

Authors and Affiliations

Siddhesh D. Patil, David G. Rhodes, Diane J. Burgess

Keywords

Related Articles

Regulation of Generic Drugs in Japan: the Current Situation and Future Prospects

Generic drugs are interchangeable with original proprietary drugs, as they have the same active pharmaceutical ingredients, dosage forms, strength, quality, indications, effects, directions, and dosage. The cost of gener...

Pharmacokinetics, Lymph Node Uptake, and Mechanistic PK Model of Near-Infrared Dye-Labeled Bevacizumab After IV and SC Administration in Mice

The online version of this article (doi:10.1208/s12248-012-9342-9) contains supplementary material, which is available to authorized users.

Preparation, characterization, and biodistribution study of technetium-99m-labeled leuprolide acetate-loaded liposomes in ehrlich ascites tumor-bearing mice

The purpose of this study was to prepare conventional and sterically stabilized liposomes containing leuprolide acetate in an attempt to prolong the biological half life of the drug, to reduce the uptake by reticuloendot...

Mechanistic Models Describing Active Renal Reabsorption and Secretion: A Simulation-Based Study

The online version of this article (doi:10.1208/s12248-012-9437-3) contains supplementary material, which is available to authorized users.

Novel Injectable Pentablock Copolymer Based Thermoresponsive Hydrogels for Sustained Release Vaccines

The online version of this article (doi:10.1208/s12248-015-9843-4) contains supplementary material, which is available to authorized users.

Download PDF file
  • EP ID EP681935
  • DOI  10.1208/aapsj060429
  • Views 80
  • Downloads 0

How To Cite

Siddhesh D. Patil, David G. Rhodes, Diane J. Burgess (2004). Anionic liposomal delivery system for DNA transfection. The AAPS Journal, 6(4), -. https://europub.co.uk/articles/-A-681935