首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >In situ enzymatic silver enhancement based on functionalized graphene oxide and layer-by-layer assembled gold nanoparticles for ultrasensitive detection of thrombin
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In situ enzymatic silver enhancement based on functionalized graphene oxide and layer-by-layer assembled gold nanoparticles for ultrasensitive detection of thrombin

机译:基于功能化氧化石墨烯和逐层组装的金纳米颗粒的原位酶银增强技术,用于凝血酶的超灵敏检测

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摘要

A highly specific in situ amplification strategy was designed for ultrasensitive detection of thrombin by combining the layer-by-layer (LBL) assembled amplification with alkaline phosphatase (ALP) and gold nanoparticles (Au) mediated silver deposition. High-density carboxyl functionalized graphene oxide (FGO) was introduced as a nanocarrier for LBL assembling of alkaline phosphatase decorated gold nanoparticles (ALP-Au), which was further adopted to label thrombin aptamer II. After sandwich-type reaction, numerous ALP were captured onto the aptasensor surface and catalyzed the hydrolysis of ascorbic acid 2-phosphate (AAP), which in situ generated ascorbic acid (AA), reducing Ag ~+ to Ag nanoparticles (AgNPs) for electrochemical readout. Inspiringly, the in situ amplification strategy with ethanolamine as an effective blocking agent showed remarkable amplification efficiency, very little nonspecific adsorption, and low background signal, which was favorable to enhance the sensitivity of aptasensor. Our novel dramatic signal amplification strategy, with a detection limit of 2.7fM, showed about 2-3 orders of magnitude improvement in the sensitivity for thrombin detection compared to other universal enzyme-based electrochemical assay.
机译:通过结合碱性磷酸酶(ALP)和金纳米颗粒(Au)介导的银沉积的逐层(LBL)组装扩增,设计了一种高度特异性的原位扩增策略,用于凝血酶的超灵敏检测。引入高密度羧基官能化氧化石墨烯(FGO)作为纳米载体,用于LBL组装碱性磷酸酶修饰的金纳米颗粒(ALP-Au),并进一步用于标记凝血酶适体II。夹心型反应后,大量ALP被捕获到适体传感器表面并催化抗坏血酸2-磷酸(AAP)的水解,后者原位生成抗坏血酸(AA),将Ag〜+还原为Ag纳米颗粒(AgNPs)进行电化学读出。令人鼓舞的是,以乙醇胺为有效封闭剂的原位扩增策略显示出显着的扩增效率,极低的非特异性吸附和低背景信号,这有利于提高适体传感器的灵敏度。我们的新颖的信号放大策略,检测极限为2.7fM,与其他基于酶的通用电化学检测方法相比,凝血酶检测的灵敏度提高了约2-3个数量级。

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