Anionic liposomal delivery system for DNA transfection

被引:0
作者
Patil S.D. [1 ,2 ]
Rhodes D.G. [1 ]
Burgess D.J. [1 ]
机构
[1] Department of Pharmaceutical Sciences, University of Connecticut, Storrs
[2] Antigenics, Lexington
关键词
Anionic liposomes; Flow cytometry; Gene delivery; Lipoplex; Nonviral vector; Transfection;
D O I
10.1208/aapsj060429
中图分类号
学科分类号
摘要
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 (lipofectAmine), 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. Copyright ©2003. All Rights Reserved.
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页数:11
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共 38 条
[1]  
Patil S.D., Burgess D.J., DNA-based biopharmaceuticals: Therapeutics for the 21st century, AAPS News Magazine, 6, (2003)
[2]  
Patil S.D., Rhodes D.G., Burgess D.J., DNA-based therapeutics and DNA delivery systems: A comprehensive review, AAPS Pharm.Sci., (2004)
[3]  
Romano G., Micheli P., Pacilio C., Giordano A., Latest developments in gene transfer technology: Achievements, perspectives, and controversies over therapeutic applications, Stem Cells, 18, 1, pp. 19-39, (2000)
[4]  
Vorburger S.A., Hunt K.K., Adenoviral gene therapy, Oncologist, 7, pp. 46-59, (2002)
[5]  
Eastman S.J., Scheule R.K., Cationic lipid:pDNA complexes for the treatment of cystic fibrosis, Curr. Opin. Mol. Ther., 1, pp. 186-196, (1999)
[6]  
Luo D., Saltzman W.M., Synthetic DNA delivery systems, Nat. Biotechnol., 18, pp. 33-37, (2000)
[7]  
Liu F., Huang L., Development of non-viral vectors for systemic gene delivery, J. Control Release, 78, 1-3, pp. 259-266, (2002)
[8]  
Kay M.A., Glorioso J.C., Naldini L., Viral vectors for gene therapy: The art of turning infectious agents into vehicles of therapeutics, Nat. Med., 7, pp. 33-40, (2001)
[9]  
Zhdanov R.I., Podobed O.V., Vlassov V.V., Cationic lipid-DNA complexes - Lipoplexes - For gene transfer and therapy, Bioelectrochemistry, 58, pp. 53-64, (2002)
[10]  
Brown M.D., Schatzlein A.G., Uchegbu I.F., Gene delivery with synthetic (non viral) carriers, Int. J. Pharm., 229, 1-2, pp. 1-21, (2001)