Department of Chemical and Biological Engineering, University of Wisconsin-Madison, 1415 Engineering Drive, Madison, WI 53706, United States.
J Colloid Interface Sci. 2012 Dec 1;387(1):56-64. doi: 10.1016/j.jcis.2012.07.083. Epub 2012 Aug 7.
We report an approach to the chemical oxidation of a ferrocene-containing cationic lipid [bis(11-ferrocenylundecyl)dimethylammonium bromide, BFDMA] that provides redox-based control over the delivery of DNA to cells. We demonstrate that BFDMA can be oxidized rapidly and quantitatively by treatment with Fe(III)sulfate. This chemical approach, while offering practical advantages compared to electrochemical methods used in past studies, was found to yield BFDMA/DNA lipoplexes that behave differently in the context of cell transfection from lipoplexes formed using electrochemically oxidized BFDMA. Specifically, while lipoplexes of the latter do not transfect cells efficiently, lipoplexes of chemically oxidized BFDMA promoted high levels of transgene expression (similar to levels promoted by reduced BFDMA). Characterization by SANS and cryo-TEM revealed lipoplexes of chemically and electrochemically oxidized BFDMA to both have amorphous nanostructures, but these lipoplexes differed significantly in size and zeta potential. Our results suggest that differences in zeta potential arise from the presence of residual Fe(2+) and Fe(3+) ions in samples of chemically oxidized BFDMA. Addition of the iron chelating agent EDTA to solutions of chemically oxidized BFDMA produced samples functionally similar to electrochemically oxidized BFDMA. These EDTA-treated samples could also be chemically reduced by treatment with ascorbic acid to produce samples of reduced BFDMA that do promote transfection. Our results demonstrate that entirely chemical approaches to oxidation and reduction can be used to achieve redox-based 'on/off' control of cell transfection similar to that achieved using electrochemical methods.
我们报告了一种方法,用于氧化含有二茂铁的阳离子脂质[双(11-二茂铁十一烷基)二甲基氯化铵,BFDMA],该方法可以提供基于氧化还原的控制,从而将 DNA 递送到细胞中。我们证明,BFDMA 可以通过用 Fe(III)硫酸盐处理而迅速且定量地被氧化。与过去研究中使用的电化学方法相比,这种化学方法具有实际优势,但研究发现,与使用电化学氧化的 BFDMA 形成的脂复合物相比,化学氧化的 BFDMA 形成的脂复合物在细胞转染的情况下表现不同。具体而言,虽然后者的脂复合物不能有效地转染细胞,但化学氧化的 BFDMA 的脂复合物促进了高水平的转基因表达(类似于还原的 BFDMA 促进的水平)。通过小角中子散射(SANS)和冷冻透射电子显微镜(cryo-TEM)的表征发现,化学和电化学氧化的 BFDMA 的脂复合物都具有无定形的纳米结构,但这些脂复合物在尺寸和 zeta 电位方面有很大的差异。我们的结果表明,zeta 电位的差异源于化学氧化的 BFDMA 样品中残留的 Fe(2+)和 Fe(3+)离子的存在。向化学氧化的 BFDMA 溶液中添加铁螯合剂 EDTA 会产生与电化学氧化的 BFDMA 功能相似的样品。用抗坏血酸处理这些 EDTA 处理的样品还可以进行化学还原,生成促进转染的还原 BFDMA 样品。我们的结果表明,可以使用完全化学方法进行氧化和还原,以实现基于氧化还原的细胞转染“开/关”控制,类似于使用电化学方法实现的控制。