基于局部表面等离子体共振的高灵敏度生物传感器中,金纳米粒子增强荧光用于测定c反应蛋白

Nhu Hoa Thi Tran, Phuong Tran, B. T. Phan, H. Tạ, Ngoc Xuan Dat Mai, Lai Thi Hoa, T. Tran, Dung V. Hoang
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引用次数: 2

摘要

c反应蛋白(CPR)是一种与许多病理相关的炎症标志物。基于荧光染色的光学生物传感器在诊断中有着广泛的应用。由于光漂白效应的存在,荧光信号的检测仍然存在一定的局限性。金纳米粒子(Au NPs)的局部表面等离子体共振(LSPR)增强了从染料分子中收集的光信号。方法:在本研究中,Au NPs具有显著的光学性能和生物相容性。种子介导的合成方法提供了具有所有基本品质的稳定的NPs。在通过越南首次引入的透射模式(t模式)检测系统进行荧光传感的生物键合之前,在玻璃基板上进行了一系列修饰步骤。结果:合成的金纳米粒子具有纳米球结构,最大吸光度为521 nm。这些变化表明,通过基本的分析方法,形成了必要的联系。最后,用Alexa 488染料检测的CRP与t模式检测的Au NPs涂层相比,平均增强因子为4.8倍。该传感器的重复性和稳定性均在0.7%以下,变异系数较低。结论:成功地开发了一种完全现代的t模系统结合LSPR用于荧光传感器增强的方法。通过改变材料的结构和成分,该传感方法具有广阔的应用前景。关键词:LSPR,金纳米粒子,荧光增强,c反应蛋白,光学生物传感器
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Gold nanoparticles enhanced fluorescence for highly sensitive biosensors based on localized surface plasmon resonance applied in determination C-reactive protein
Introduction: C-reactive protein (CPR) is known as an inflammation marker related to numerous pathology. Optical biosensor based on the fluorescence dyed is widely used in diagnosis. There are still limitations on the fluorescence signal detection due to the photobleaching effect. The localized surface plasmon resonance (LSPR) performed by gold nanoparticles (Au NPs) is testified for the enhancement of photo-signal gathered from the dye molecules. Methods: In this study, Au NPs were used for their significant optical properties and biocompatibility additionally. The seed-mediated synthesis method provided stable NPs with all the essential qualities. A series of modification steps were done on a glass substrate before the bio-bonding for fluorescence-based sensing by a transmission mode (T-mode) detection system which is introduced for the first time in Viet Nam. Results: The synthetic Au NPs in nanosphere structure evinced the absorbance at a maximum wavelength is 521 nm. All the followed alterations showed the accomplishment in forming the in need linking proved through the basic analysis methods. Finally, CRP with the Alexa 488 dye was observed for average at 4.8 folds of enhancement factor compared between the Au NPs coating and non-coating substrate detected by the T-mode system. The low coefficient of variation at under 0.7% appeared for the repeatability and stability of this sensor. Conclusion: The completely modern approach of the T-mode system combined with the LSPR applied in fluorescence sensors enhanced is developed successfully. Also, the future prospect of this designed sensing method is promising by changing the materials' structures and ingredients. Keywords: LSPR, gold nanoparticles, fluorescence enhancement, C-reaction protein, optical biosensors
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