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Surface anchoring of liquid crystals in contact with functionalized organic thin films.

机译:液晶与功能化有机薄膜接触的表面锚固。

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The research activities that are summarized in this dissertation aim to elucidate principles that permit the development of sensitive and quantitative analytical methods using liquid crystals to report the highly selective capture of biomolecular analytes at surfaces. These principles are based on the following past observations: (1) the orientations of liquid crystals near surfaces are sensitive to subtle changes in interfacial energy (10-9 J/m2 to 10-3 J/m2), (2) the binding of biomolecular analytes to surfaces can drive the reorientation of films of liquid crystals of thickness ≥100 mum, (3) changes in the orientations of liquid crystals can be measured using polarized light microscopy and (4) self-assembled monolayers formed from oligo(ethylene glycol)-terminated thiols that are supported on gold films form the basis of functional surfaces that can resist (or partially) resist the non-specific adsorption of proteins.; This thesis investigates: (I) the orientational behavior of a nematic liquid crystal in contact with oligo(ethylene glycol)-terminated self-assembled monolayers, (II) the amplification of protein-peptide binding events at oligo(ethylene glycol)-terminated self-assembled monolayers using liquid crystals, (III) the methodology to obtain a quantitative measurement of an intrinsic property of the liquid crystal/monolayer interface, i.e. azimuthal anchoring energy, (IV) the application of that methodology to quantify changes in the azimuthal anchoring energy of the liquid crystal/monolayer interface upon incremental addition of biomolecular analyte, (V) a low-cost surface preparation for the precise control of the out-of-plane alignment of liquid crystals over macroscopic distances and (VI) a preliminary study of using liquid crystals to image fibroblast cells that are adhered to functionalized oligo(ethylene glycol)-terminated self-assembled monolayers.; The results of this research, when combined, form the basis of quantitative analytical methods using liquid crystals for the study of biomolecular analytes that are present in complex biological fluids.
机译:本文总结的研究活动旨在阐明一些原理,这些原理允许开发使用液晶的灵敏和定量分析方法,以报告对表面生物分子分析物的高度选择性捕获。这些原理基于以下过去的观察结果:(1)表面附近液晶的取向对界面能的细微变化(10-9 J / m2至10-3 J / m2)敏感,(2)生物分子分析物到表面可以驱动厚度≥100μm的液晶膜重新取向,(3)可以使用偏振光显微镜测量液晶的取向变化,以及(4)由低聚乙二醇形成的自组装单层膜)负载在金膜上的末端巯基构成了可以抵抗(或部分抵抗)蛋白质非特异性吸附的功能性表面的基础。本论文研究:(I)向列型液晶与低聚(乙二醇)终止的自组装单层接触的取向行为,(II)在低聚(乙二醇)终止的自组装单层上蛋白质-肽结合事件的放大使用液晶组装的单层膜,(III)用于定量测量液晶/单层界面固有特性(即方位锚定能)的方法,(IV)该方法的应用以量化方位锚定能的变化增量添加生物分子分析物时液晶/单层界面的变化;(V)低成本表面处理,可在宏观距离上精确控制液晶的平面外对准;(VI)使用的初步研究液晶成像成纤维细胞,该成纤维细胞粘附在功能化的寡聚(乙二醇)末端自组装单层膜上。这项研究的结果相结合,构成了使用液晶定量分析方法研究复杂生物流体中存在的生物分子分析物的基础。

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