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The design of poly(tert-butyl acrylate) networks for biomedical applications.

机译:用于生物医学的聚(丙烯酸叔丁酯)网络的设计。

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The organization of this Dissertation is as follows. Chapter 1 serves an introduction to polymer networks. Different types of networks are described, as well as some relevant theoretical models used to characterize such networks. Chapter 2 discusses how different curing processes affect the final network structures of poly(tert-butyl acrylate) (poly( t-BA)) gels. Specifically, uncovered and covered molds are investigated in order to see how evaporation of the precursor solution effects the final network structure. Different curing temperatures as well as different amounts and qualities of solvents are also explored. Rheological and swelling experiments are used in conjunction with equilibrium swelling theories in order to deduce poly(t-BA) network structure. Chapter 3 discusses the biocompatibility of various poly(t-BA) topographies, namely brushes formed by both spin coating and supercritical carbon dioxide, and crosslinked networks. This investigation explored the possibility of using poly(t-BA) as a biomaterial as well as answering the question of how thin we can make polymer coatings before the cells begin to respond to the underlying surface beneath the polymer layer. Chapter 4 discusses the synthesis of end-linked networks, which are far more homogeneous in nature than networks made by free radical polymerization. One approach taken is the so-called "click chemistry" approach is discussed and results in networks that have very well-defined molecular weights between crosslinks. These end-linking procedures leads to an easy and reliable approach for making homogeneous, networks. Chapter 5 concludes this Dissertation with a summary with possible future outlooks.
机译:本论文的组织如下。第1章介绍聚合物网络。描述了不同类型的网络,以及用于表征此类网络的一些相关理论模型。第2章讨论了不同的固化工艺如何影响聚丙烯酸叔丁酯(t-BA)凝胶的最终网络结构。具体而言,对未覆盖和覆盖的模具进行了研究,以了解前体溶液的蒸发如何影响最终的网络结构。还探索了不同的固化温度以及不同数量和质量的溶剂。流变和溶胀实验与平衡溶胀理论结合使用,以推导聚(t-BA)网络结构。第3章讨论了各种聚(t-BA)形貌的生物相容性,即由旋涂和超临界二氧化碳和交联网络形成的刷子。这项研究探索了使用聚(t-BA)作为生物材料的可能性,并回答了在细胞开始响应聚合物层下方的下层表面之前,我们可以将聚合物涂层制成多薄的问题。第4章讨论了末端连接网络的合成,这些末端连接网络本质上比自由基聚合制得的网络更均匀。所采取的一种方法是讨论所谓的“点击化学”方法,其结果是在交联之间具有非常明确定义的分子量的网络。这些末端链接程序导致一种简单可靠的方法来制作同类网络。第五章以总结性总结了未来的展望。

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