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Physical characterization of erodible multilayered polyelectrolyte thin films fabricated from plasmid DNA and synthetic polyamines.

机译:由质粒DNA和合成多胺制备的易蚀多层聚电解质薄膜的物理表征。

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摘要

This thesis focuses on the physical characterization of morphological transformations that occur in erodible multilayered polyelectrolyte films fabricated by the layer-by-layer deposition of plasmid DNA and synthetic polyamines, using atomic force microscopy (AFM), scanning electron microscopy (SEM), and laser scanning confocal microscopy (LSCM). When incubated in aqueous media, these ultrathin (∼100 nm thick) films gradually erode and release DNA over periods of approximately 48 hours. Characterization by AFM and SEM revealed that these films transform from an initially smooth morphology to one that is characterized by interconnected ridges and valleys. Further incubation results in the decomposition of these features into nanoparticulate structures. The patterns and structures generated by this transformation are similar to those observed for the spinodal dewetting of thin films of conventional polymers. This behavior has not, however, been observed for this class of multilayered assemblies, for which long-range electrostatic interactions play significant roles in governing film structure and stability. The results of additional experiments demonstrate that it is possible to promote this behavior, prevent it, or control it by varying polymer structure, film composition, or the conditions to which these materials are exposed. The results of experiments using LSCM and AFM to characterize films fabricated using fluorescently labeled polyelectrolytes suggest a physical picture of the nanoparticulate morphology in which polyelectrolyte layers from the topmost portion of the film remain relatively undisturbed and are juxtaposed over an array of particulate structures formed by polyelectrolyte chains from the bottommost layers of the film. Investigations of the influence of film thickness on the characteristic length scales associated with this transformation revealed a complex relationship that did not follow trends derived from models developed to describe the spinodal dewetting of thin films of conventional materials. The results presented in this thesis suggest the basis of methods that could prove useful for the generation of nanostructure on complex surfaces and contribute to methods for the localized delivery of DNA from surfaces.
机译:本论文的重点是通过原子力显微镜(AFM),扫描电子显微镜(SEM)和激光通过逐层沉积质粒DNA和合成多胺制备的易蚀多层聚电解质膜中发生的形态转变的物理表征。扫描共聚焦显微镜(LSCM)。当在水性介质中孵育时,这些超薄(约100 nm厚)膜会逐渐腐蚀并在大约48小时内释放出DNA。通过AFM和SEM进行的表征表明,这些薄膜从最初的平滑形态转变为以相互连接的凸脊和凹谷为特征的薄膜。进一步温育导致这些特征分解成纳米颗粒结构。通过这种转变产生的图案和结构类似于常规聚合物薄膜的旋节线去湿所观察到的那些。但是,对于此类多层组件,尚未观察到这种行为,对于这种组件,长距离静电相互作用在控制薄膜结构和稳定性方面起着重要作用。其他实验的结果表明,可以通过改变聚合物的结构,膜的成分或这些材料所处的条件来促进,防止或控制这种行为。使用LSCM和AFM表征使用荧光标记的聚电解质制备的薄膜的实验结果表明,纳米颗粒形态的物理图像,其中薄膜最顶部的聚电解质层保持相对不受干扰,并列在由聚电解质形成的一系列颗粒结构上薄膜最底层的链条。薄膜厚度对与这种转变有关的特征长度尺度的影响的研究表明,这种复杂的关系并不遵循从描述传统材料薄膜的旋节线去湿所开发的模型得出的趋势。这篇论文提出的结果提出了可能被证明对在复杂表面上产生纳米结构有用的方法的基础,并有助于从表面上局部递送DNA的方法。

著录项

  • 作者

    Fredin, Nathaniel Jon.;

  • 作者单位

    The University of Wisconsin - Madison.;

  • 授予单位 The University of Wisconsin - Madison.;
  • 学科 Engineering Chemical.
  • 学位 Ph.D.
  • 年度 2008
  • 页码 248 p.
  • 总页数 248
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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