Fredin Nathaniel J, Zhang Jingtao, Lynn David M
Department of Chemical and Biological Engineering, University of Wisconsin-Madison, 1415 Engineering Drive, Madison, Wisconsin 53706-1607, USA.
Langmuir. 2005 Jun 21;21(13):5803-11. doi: 10.1021/la050596+.
Atomic force microscopy (AFM) and scanning electron microscopy (SEM) coupled with ellipsometry have been used to characterize the microscale and nanoscale structures of erodible multilayered films fabricated from degradable polyamine 1 and either sodium poly(styrene sulfonate) (SPS) or plasmid DNA. Striking differences were found in the topography, structures, and erosion profiles of these two materials upon incubation in PBS buffer at 37 degrees C. For films fabricated from SPS, AFM data are consistent with an erosion process that occurs uniformly without the generation of holes or pits over large, micrometer-scale areas. By contrast, films fabricated from plasmid DNA undergo structural rearrangements to present surface-bound particles ranging in size from 50 to 400 nm. Additional characterization of these particulate structures by SEM suggested that they are interpenetrated with or fused to underlying polyelectrolyte layers on the silicon surface, providing a potential mechanism to manipulate the adhesive forces with which these particles are bound to the surface. The erosion profile observed for polymer 1/SPS films suggests that it may be possible to design assemblies that release two film components with well-defined release kinetics. In the context of gene delivery, the presentation of condensed DNA as nanoparticles at these surfaces may be advantageous with respect to stimulating the internalization and processing of DNA by cells. A quantitative understanding of the factors influencing the fabrication, structure, and erosion profiles of these materials will be useful for the design of multilayered assemblies for specific applications in which controlled film erosion or the release of therapeutic materials is desired.
原子力显微镜(AFM)以及结合椭偏仪的扫描电子显微镜(SEM)已被用于表征由可降解聚胺1与聚(苯乙烯磺酸钠)(SPS)或质粒DNA制备的可侵蚀多层膜的微观和纳米尺度结构。在37℃下于PBS缓冲液中孵育时,发现这两种材料在形貌、结构和侵蚀轮廓上存在显著差异。对于由SPS制备的膜,AFM数据与一种侵蚀过程一致,该过程均匀发生,在大面积的微米尺度区域上不会产生孔洞或凹坑。相比之下,由质粒DNA制备的膜会发生结构重排,呈现出尺寸范围为50至400 nm的表面结合颗粒。通过SEM对这些颗粒结构的进一步表征表明,它们与硅表面上的底层聚电解质层相互渗透或融合,这提供了一种潜在机制来操控这些颗粒与表面结合的粘附力。观察到的聚合物1/SPS膜的侵蚀轮廓表明,有可能设计出能以明确的释放动力学释放两种膜成分的组装体。在基因递送的背景下,在这些表面将浓缩的DNA呈递为纳米颗粒对于刺激细胞对DNA的内化和加工可能是有利的。对影响这些材料的制备、结构和侵蚀轮廓的因素进行定量理解,对于设计用于特定应用的多层组装体将是有用的,在这些应用中需要可控的膜侵蚀或治疗材料的释放。