DQAsomes:: A novel potential drug and gene delivery system made from Dequalinium™

被引:151
作者
Weissig, V [1 ]
Lasch, J
Erdos, G
Meyer, HW
Rowe, TC
Hughes, J
机构
[1] Massachusetts Gen Hosp, Ctr Imaging & Pharmaceut Res, Charlestown, MA USA
[2] Harvard Univ, Sch Med, Charlestown, MA USA
[3] Univ Halle Wittenberg, Inst Physiol Chem, Halle, Germany
[4] Univ Florida, Interdisciplinary Ctr Biotechnol Res, Gainesville, FL 32611 USA
[5] Univ Jena, Inst Ultrastruct Res, D-6900 Jena, Germany
[6] Univ Florida, Dept Therapeut & Pharmacol, Sch Med, Gainesville, FL 32611 USA
[7] Univ Florida, Sch Pharm, Dept Pharmaceut, Gainesville, FL 32611 USA
关键词
dequalinium; liposome; bolaform drug; non-viral transfection vector; gene therapy; drug delivery;
D O I
10.1023/A:1011991307631
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose. Dequalinium, a drug known for over 30 years, is a dicationic amphiphile compound resembling bolaform electrolytes. The purpose of our work was to determine the state of aggregation of dequalinium in aqueous medium and to investigate both, its ability to bind DNA and its potential to serve as a novel non-viral transfection vector. Methods. The form of aggregation was determined employing electron microscopic techniques. The DNA binding capacity of dequalinium was assayed using SYBR(TM) Green I stain. For in vitro cell transfection experiments plasmid DNA encoding for firefly luciferase was used. Results, Dequalinium forms in aqueous medium liposome-like aggregates, which we term DQAsomes. These dequalinium vesicles bind DNA and they are able to transfect cells in vitro with an efficiency comparable to Lipofectin(TM). Conclusions. Based on the intrinsic properties of dequalinium such as the in vivo selectivity for carcinoma cells and selective accumulation in mitochondria we propose DQAsomes as a novel and unique drug and gene delivery system.
引用
收藏
页码:334 / 337
页数:4
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