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Matrix-Independent Surface-Enhanced Raman Scattering Detection of Uranyl Using Electrospun Amidoximated Polyacrylonitrile Mats and Gold Nanostars

机译:静电纺丝的ox肟化聚丙烯腈毡和金纳米星对铀基的基质独立表面增强拉曼散射检测

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摘要

Reproducible detection of uranyl, an important biological and environmental contaminant, from complex matrixes by surface-enhanced Raman scattering (SERS) is successfully achieved using amidoximated-polyacrylonitrile (AO-PAN) mats and carboxylated gold (Au) nanostars. SERS detection of small molecules from a sample mixture is traditionally limited by nonspecific adsorption of nontarget species to the metal nanostructures and subsequent variations in both the vibrational frequencies and intensities. Herein, this challenge is overcome using AO-PAN mats to extract uranyl from matrixes ranging in complexity including HEPES buffer, Ca(NO3)2 and NaHCO3 solutions, and synthetic urine. Subsequently, Au nanostars functionalized with carboxyl-terminated alkanethiols are used to enhance the uranyl signal. The detected SERS signals scale with uranyl uptake as confirmed using liquid scintillation counting. SERS vibrational frequencies of uranyl on both hydrated and lyophilized polymer mats are largely independent of sample matrix, indicating less complexity in the uranyl species bound to the surface of the mats vs in solution. These results suggest that matrix effects, which commonly limit the use of SERS for complex sample analysis, are minimized for uranyl detection. The presented synergistic approach for isolating uranyl from complex sample matrixes and enhancing the signal using SERS is promising for real-world sample detection and eliminates the need of radioactive tracers and extensive sample pretreatment steps.
机译:使用酰胺肟化聚丙烯腈(AO-PAN)垫和羧化金(Au)纳米星成功地实现了表面增强拉曼散射(SERS)从复杂基质中可重复检测铀酰(一种重要的生物和环境污染物)的作用。传统上,SERS从样品混合物中检测小分子受到非目标物质对金属纳米结构的非特异性吸附以及振动频率和强度的随后变化的限制。在本文中,使用AO-PAN垫克服了这一挑战,它从复杂的基质(包括HEPES缓冲液,Ca(NO3)2和NaHCO3溶液以及合成尿液)中提取铀酰。随后,被羧基末端的链烷硫醇官能化的金纳米星被用于增强铀酰信号。检测到的SERS信号随尿嘧啶摄取而缩放,这已通过液体闪烁计数得到了证实。在水合和冻干的聚合物垫上,铀酰的SERS振动频率在很大程度上与样品基质无关,这表明与溶液相比,与垫表面结合的铀酰种类的复杂性较低。这些结果表明,通常限制将SERS用于复杂样品分析的基质效应可最小化用于铀酰检测。提出的用于从复杂样品基质中分离铀酰并使用SERS增强信号的协同方法有望用于实际样品检测,并且无需放射性示踪剂和大量样品预处理步骤。

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