首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >Turn-on colorimetric sensor for ultrasensitive detection of thrombin using fibrinogen-gold nanoparticle conjugate
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Turn-on colorimetric sensor for ultrasensitive detection of thrombin using fibrinogen-gold nanoparticle conjugate

机译:开启式比色传感器,用于使用纤维蛋白原-金纳米颗粒共轭物超灵敏地检测凝血酶

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摘要

A simple, colorimetric 'turn on' sensor for ultrasensitive detection of thrombin has been developed using fibrinogen-modified gold nanoparticles (Fib-Au NPs). The assay was based on the thrombin-fibrinogen interaction which is part of the physiological process of blood clotting. The fibrinogen was immobilized on the surface of 96-well plate offering reactive N-oxysuccinimide esters (referred to as NOS group) surface. Introducing thrombin and Fib-Au NPs into the fibrinogen-bound 96-well plate induced the immobilization of Fib-Au NPs on the surface of 96-well plate through the thrombin mediated conversion of soluble fibrinogen to insoluble cross-linked fibrin. Such process could be detected visually post HAuCl_4-NH_2OH redox reaction catalyzed by the Au NPs. The parameters governing the performance of the assay have been optimized. The detection limit was 3.2 fM, corresponding to 0.16 amol thrombin in 50 μL of sample. Other proteins, such as bovine serum albumin (BSA), pepsin, trypsin, hemoglobin, lysozyme, and cytochrome c did not show interference with the assay of thrombin. In addition, the work demonstrates the feasibility of thrombin detection in a complex matrix, showing potential for rapid medical diagnostics.
机译:使用纤维蛋白原修饰的金纳米颗粒(Fib-Au NP),开发了一种用于凝血酶超灵敏检测的简单的比色“开启”传感器。该测定基于凝血酶-纤维蛋白原相互作用,这是血液凝固的生理过程的一部分。将纤维蛋白原固定在96孔板的表面上,以提供反应性的N-氧琥珀酰亚胺酯(称为NOS基团)表面。将凝血酶和Fib-Au NPs引入到纤维蛋白原结合的96孔板中,通过凝血酶介导的可溶性纤维蛋白原向不溶性交联纤维蛋白的转化,将Fib-Au NPs固定在96孔板的表面上。 Au NPs催化的HAuCl_4-NH_2OH氧化还原反应可以目视检测到。控制测定性能的参数已经过优化。检测极限为3.2 fM,对应于50μL样品中的0.16 amol凝血酶。其他蛋白质,例如牛血清白蛋白(BSA),胃蛋白酶,胰蛋白酶,血红蛋白,溶菌酶和细胞色素c,对凝血酶的测定没有干扰。此外,这项工作还证明了在复杂基质中检测凝血酶的可行性,显示了进行快速医学诊断的潜力。

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