Sharma Vishnu Dutt, Lees Julia, Hoffman Nicholas E, Brailoiu Eugen, Madesh Muniswamy, Wunder Stephanie L, Ilies Marc A
Department of Pharmaceutical Sciences and Moulder Center for Drug Discovery Research, Temple University School of Pharmacy , 3307 N. Broad Street, Philadelphia, Pennsylvania 19140, United States.
Mol Pharm. 2014 Feb 3;11(2):545-59. doi: 10.1021/mp4005035. Epub 2014 Jan 6.
The study presents the effects of blending a cationic gemini surfactant into cationic lipid bilayers and its impact on the plasmid DNA compaction and delivery process. Using nanoDSC, dynamic light scattering, zeta potential, and electrophoretic mobility measurements, together with transfection (2D- and 3D-) and viability assays, we identified the main physicochemical parameters of the lipid bilayers, liposomes, and lipoplexes that are affected by the gemini surfactant addition. We also correlated the cationic bilayer composition with the dynamics of the DNA compaction process and with transfection efficiency, cytotoxicity, and the internalization mechanism of the resultant nucleic acid complexes. We found that the blending of gemini surfactant into the cationic bilayers fluidized the supramolecular assemblies, reduced the amount of positive charge required to fully compact the plasmid DNA and, in certain cases, changed the internalization mechanism of the lipoplexes. The transfection efficiency of select ternary lipoplexes derived from cationic gemini surfactants and lipids was several times superior to the transfection efficiency of corresponding binary lipoplexes, also surpassing standard transfection systems. The overall impact of gemini surfactants into the formation and dynamic of cationic bilayers was found to depend heavily on the presence of colipids, their nature, and amount present in lipoplexes. The study confirmed the possibility of combining the specific properties of pyridinium gemini surfactants and cationic lipids synergistically to obtain efficient synthetic transfection systems with negligible cytotoxicity useful for therapeutic gene delivery.
该研究展示了将阳离子双子表面活性剂混入阳离子脂质双层的效果及其对质粒DNA压缩和递送过程的影响。通过纳米差示扫描量热法、动态光散射、ζ电位和电泳迁移率测量,以及转染(二维和三维)和活力测定,我们确定了受双子表面活性剂添加影响的脂质双层、脂质体和脂质复合物的主要物理化学参数。我们还将阳离子双层组成与DNA压缩过程的动力学以及转染效率、细胞毒性和所得核酸复合物的内化机制相关联。我们发现,将双子表面活性剂混入阳离子双层会使超分子组装体流化,减少完全压缩质粒DNA所需的正电荷量,并且在某些情况下会改变脂质复合物的内化机制。源自阳离子双子表面活性剂和脂质的特定三元脂质复合物的转染效率比相应二元脂质复合物的转染效率高出数倍,也超过了标准转染系统。研究发现,双子表面活性剂对阳离子双层形成和动态的总体影响在很大程度上取决于共脂质的存在、其性质以及在脂质复合物中的含量。该研究证实了协同结合吡啶鎓双子表面活性剂和阳离子脂质的特定特性以获得具有可忽略细胞毒性的高效合成转染系统用于治疗性基因递送的可能性。