Jewell Christopher M, Lynn David M
Department of Chemical and Biological Engineering, University of Wisconsin - Madison 1415 Engineering Drive, Madison, WI 53706, USA.
Curr Opin Colloid Interface Sci. 2008 Dec;13(6):395-402. doi: 10.1016/j.cocis.2008.03.005.
The last several years have seen a significant increase in the number of reports describing the use of cationic polymers to design new materials and nanoscale assemblies that promote the surface-mediated delivery of DNA to cells and tissues. In general, these approaches fall into one of two broad categories: (i) methods based upon the physical adsorption of preformed, colloidal aggregates of cationic polymer and DNA (polyplexes) to surfaces, and (ii) methods for the layer-by-layer adsorption of DNA and cationic polymers on surfaces to fabricate multilayered thin films that provide control over the release of DNA into solution or to cells. In this Opinion, we discuss several recent examples of each of these approaches and provide commentary on ways in which the physical and chemical behaviours of cationic polymers have played key roles and present future opportunities to develop new methods for localized and surface-mediated cell transfection in vitro and in vivo.
在过去几年中,描述使用阳离子聚合物设计新材料和纳米级组装体的报告数量显著增加,这些新材料和组装体可促进DNA通过表面介导递送至细胞和组织。一般来说,这些方法可分为两大类:(i)基于阳离子聚合物和DNA的预制胶体聚集体(多聚体)物理吸附到表面的方法,以及(ii)在表面逐层吸附DNA和阳离子聚合物以制造多层薄膜的方法,这些薄膜可控制DNA释放到溶液或细胞中。在本观点文章中,我们讨论了每种方法的几个近期实例,并对阳离子聚合物的物理和化学行为发挥关键作用的方式进行了评论,还提出了在体外和体内开发用于局部和表面介导细胞转染的新方法的未来机会。