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用于单纳米粒子等离子体生物传感器的距离可调 Au 纳米棒芯片的简易制造。

Facile fabrication of distance-tunable Au-nanorod chips for single-nanoparticle plasmonic biosensors.

机构信息

School of Chemical and Biomedical Engineering, Nanyang Technological University, 637457, Singapore.

出版信息

Biosens Bioelectron. 2011 Jan 15;26(5):2246-51. doi: 10.1016/j.bios.2010.09.042. Epub 2010 Sep 29.

Abstract

In this work, we present a simple and effective method to fabricate distance-controllable, Au nanorod (AuNR) chips thorough electrostatic assembly. Cetyltrimethylammonium bromide (CTAB)-capped AuNRs were immobilized on a hydroxyl-functionalized glass substrate by immersion of the glass into AuNR-suspension. The electrostatic surfacial assembly of AuNRs offers significant advantages over conventional thiol-induced chemistry, i.e., direct control of self-assembly of AuNRs, easy fabrication in ambient environment and most importantly, broad range of tunable inter-particle distance, ranging from 0.25 to 10 μm. The mechanism of time-dependant deposition process of AuNRs was described via competitive bindings of AuNRs and free CTAB molecules in AuNR-suspension. In addition, the electrostatically anchored AuNRs on a glass substrate provide sufficient stability under harsh experimental conditions with flow of basic/acidic solutions and organic solvents with different polarity. The feasibility of the AuNR-chips fabricated by the proposed method for single-nanoparticle plasmonic biosensors was demonstrated by the plasmonic measurement of aptamer-thrombin binding event. The corresponding limit of detection of thrombin molecule was found to be ∼278 pM based on the signal to noise ratio of 4.

摘要

在这项工作中,我们提出了一种简单有效的方法,通过静电组装来制造距离可控的金纳米棒(AuNR)芯片。十六烷基三甲基溴化铵(CTAB)封端的 AuNR 通过将玻璃浸入 AuNR 悬浮液中而固定在羟基功能化的玻璃基底上。与传统的硫醇诱导化学相比,AuNR 的静电表面组装具有显著的优势,即可以直接控制 AuNR 的自组装、在环境条件下易于制造,最重要的是,具有广泛的可调谐粒子间距离,范围从 0.25 到 10 μm。通过 AuNR 悬浮液中 AuNR 和游离 CTAB 分子的竞争结合,描述了 AuNR 沉积过程随时间的变化机制。此外,在碱性/酸性溶液和不同极性有机溶剂的流动等苛刻实验条件下,静电固定在玻璃基底上的 AuNR 具有足够的稳定性。通过等离子体测量适配体-凝血酶结合事件,证明了所提出的方法制造的 AuNR 芯片用于单纳米颗粒等离子体生物传感器的可行性。基于信噪比为 4,检测到凝血酶分子的相应检测限约为 278 pM。

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