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Simultaneous Surface Plasmon Resonance/Fluorescence Spectroelectrochemical in Situ Monitoring of Dynamic Changes on Functional Interfaces: A Study of the Electrochemical Proximity Assay Model System

机译:同时表面等离子体共振/荧光光谱电化学原位监测功能界面的动态变化:电化学近距离测定模型系统的研究

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摘要

Understanding the chemical composition and morphology of interfaces plays a vital role in the development of sensors, drug delivery systems, coatings for biomedical implants, and so forth. In many cases, the interface characterization can be performed by a combination of electrochemical and one of the optical techniques. In this study, we further enhanced capabilities in probing interfaces by combining electrochemical characterization with multiple optical techniques, that is, surface plasmon resonance (SPR) and fluorescence spectroscopy. This new combination was utilized to study the electrochemical proximity assay (ECPA)-a recently developed protein recognition strategy for the point-of-care test. The SPR/fluorescence spectroelectrochemical technique has achieved not only recognition of binding components involved in the ECPA model system, estimation of their thicknesses and surface coverages, but more importantly, highly reliable in situ monitoring of dynamic changes of components involved in interfacial binding via cross-validation and confirmation from three simultaneously generated signals-SPR, fluorescence, and electrochemistry. In addition, the obtained corresponding proportions among magnitudes of three signals provide crucial information for future studies on simultaneous characterization of multiple components in one step and differentiation of nonspecific binding events. Another advantage using this technique is that the excitation of fluorescence is not only confined by surface plasmons, but by photons, so the fluorescence information can be also gained as the distance of fluorophores from the surface exceeds the decay length of surface plasmons.
机译:理解界面的化学成分和形态在发育传感器,药物递送系统,生物医学植入物的涂层的发展中起着至关重要的作用。在许多情况下,界面表征可以通过电化学和一种光学技术之一来执行。在这项研究中,我们通过用多种光学技术组合电化学表征来进一步增强探测界面的能力,即表面等离子体共振(SPR)和荧光光谱。这种新组合用于研究电化学邻近测定(ECPA)-A最近开发的蛋白质识别策略进行护理点测试。 SPR /荧光光谱电化学技术不仅识别ECPA模型系统中涉及的结合组分,它们的厚度和表面覆盖物的估计,而且更重要地,高度可靠地理发监测通过交叉的界面结合所涉及的部件的动态变化从三个同时产生的信号-SH,荧光和电化学验证和确认。另外,在三个信号的大小之间获得的相应比例为未来的研究提供了关于多个组分在一步中的同时表征的关键信息和非特异性结合事件的分化。使用该技术的另一个优点是荧光的激发不仅由表面等离子体限制,而是通过光子限制,因此可以在从表面荧光团的距离超过表面等离子体的衰减长度时获得荧光信息。

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