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Benchtop chemistry for the rapid prototyping of label-free biosensors: Transmission localized surface plasmon resonance platforms

机译:用于无标签生物传感器快速原型化的台式化学方法:透射局部表面等离子体共振平台

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Herein, a simple label-free biosensor fabrication method is demonstrated based on transmission localized surface plasmon resonance (T-LSPR). The platform, which consists of a silver nanoparticle array, can be prepared in just a few minutes using benchtop chemistry. The array was made by a templating technique in conjunction with the photoreduction of Ag ions from solution. This metal surface was functionalized with biotin-linked thiol ligands for binding streptavidin molecules from solution. For an array of 19 nm diameter silver nanoparticles, a redshift in the T-LSPR spectrum of 24 nm was observed upon protein-ligand binding at saturation. The binding constant was found to be 2 × 1012 M?1. Platforms were also fabricated with silver nanoparticles of 34, 55, and 72 nm diameters. The maximum LSPR wavelength shift was nanoparticle size dependent and the maximum sensitivity was obtained with the smaller nanoparticles.
机译:本文中,基于透射局部表面等离子体共振(T-LSPR),展示了一种简单的无标记生物传感器制造方法。该平台由银纳米颗粒阵列组成,可以使用台式化学方法在短短几分钟内完成制备。该阵列是通过模板技术结合银离子从溶液中光还原而制成的。该金属表面用生物素连接的硫醇配体官能化,以结合溶液中的链霉亲和素分子。对于直径为19 nm的银纳米颗粒的阵列,在饱和状态下观察到蛋白质-配体结合后,在24 nm的T-LSPR光谱中观察到红移。发现结合常数为2×1012M·1。平台也用直径为34、55和72 nm的银纳米颗粒制成。最大的LSPR波长偏移取决于纳米颗粒的大小,使用较小的纳米颗粒可获得最大的灵敏度。

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