首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Inhibition of catalytic activity of fibrinogen-stabilized gold nanoparticles via thrombin-induced inclusion of nanoparticle into fibrin: Application for thrombin sensing with more than 10(4)-fold selectivity
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Inhibition of catalytic activity of fibrinogen-stabilized gold nanoparticles via thrombin-induced inclusion of nanoparticle into fibrin: Application for thrombin sensing with more than 10(4)-fold selectivity

机译:通过凝血酶诱导的纳米粒子纳入纤维蛋白的催化活性抑制纤维蛋白酶稳定的金纳米颗粒的催化活性:血栓性感测的施用超过10(4)

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摘要

Citrate-capped gold nanoparticles (AuNPs) modified with thrombin-binding aptamer are often implemented for colorimetric, fluorescent, and electrochemical detection of thrombin in an aqueous solution. However, researchers have rarely explored the application of fibrinogen-modified AuNPs (F-AuNPs) for thrombin sensing. We present a simple, inexpensive, sensitive, and selective probe for colorimetric assay of thrombin through combining thrombin-induced inclusion of F-AuNPs into Fibrin and F-AuNPs-catalyzed reduction of 4-nitrophenol with an excess amount of NaBH4. Considering that fibrinogen stabilized citrate-capped AuNPs against a high ionic -strength buffer, F-AuNPs efficiently catalyzed the NaBH4-mediated decrease of yellow 4-nitrophenol to colorless 4-aminophenol. The presence of thrombin converted fibrinogen into fibrin on the nanoparticle surface, leading to the inclusion of nanoparticles into fibrin. The formation of fibrin inhibited that the AuNPs catalyzed the NaBH4-mediated reduction of 4-nitrophenol. Consequently, the color of the solution gradually varied from colorless to yellow with increasing thrombin concentration. The proposed system was shown to be accurate in the quantification of small differences in the concentration of human thrombin over the range of 4-60 mu M. The lowest detectable concentration of human thrombin by the naked eye was as low as 16 mu M. We demonstrated the practical application of the proposed system in quantifying 1-15 nM human thrombin in human plasma. (C) 2018 Elsevier B.V. All rights reserved.
机译:与凝血酶结合适配子改性柠檬酸盐封端的金粒子(AuNPs)通常用于在水溶液中比色,荧光和电化学检测的凝血酶实现。然而,研究人员已经很少探讨了凝血酶传感纤维蛋白原修饰的AuNP(F-金纳米粒子)的应用。我们通过结合凝血酶诱导的夹杂物F-的AuNP的成纤维蛋白和提出了一个简单的,廉价的,敏感的,并且选择性探针凝血酶比色测定F-的AuNP催化的还原4-硝基苯酚的用NaBH4过量。考虑对高离子-Strength缓冲纤维蛋白原稳定化的柠檬酸盐封端的AuNP,F-的AuNP有效地催化黄色4-硝基苯酚的无色4-氨基苯酚的加入NaBH 4介导的降低。凝血酶纤维蛋白原转化的存在下成纤维蛋白纳米粒子表面上,从而导致包含纳米颗粒的成纤维蛋白。纤维蛋白的形成抑制了纳米金催化4-硝基苯酚的加入NaBH 4介导的降低。因此,溶液的颜色逐渐从无色变化到黄色与凝血酶浓度的增加。所提出的系统被证明是在凝血酶超过4-60亩M.人凝血酶的最低检测浓度通过肉眼的范围在人类的浓度小的差异定量准确低至16亩M.我们证明在定量1-15 nM的人凝血酶在人血浆中所提出的系统的实际应用。 (c)2018年elestvier b.v.保留所有权利。

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