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Investigation of plasmonic signal enhancement based on long range surface plasmon resonance with gold nanoparticle tags

机译:基于金纳米粒子标签的长距离表面等离子体共振的等离子体信号增强研究

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Gold nanoparticle (AuNP) molecular tags yield a significant signal enhancement in SPR-based immunoassays. While the structure functions of the AuNP tags have been exhaustively investigated, the roles of the evanescent field intensity and distribution remains to be elucidated. Long range surface plasmon resonance (LRSPR) possesses significantly larger fields and longer penetration depth than conventional SPR (cSPR). We report here on the optimization of AuNP tag LRSPR signal enhancement immunoassays using both theoretical simulations built using the finite element method and experimental measurements. A model sandwich immunoassay for the carcinoembryonic antigen (CEA) was then used to demonstrate the feasibility of AuNP tag enhanced LRSPR. The experimental measurements were in excellent agreement with the theoretical model and up to 50-fold improvement in sensitivity was obtained when using 50 nm AuNP tags in comparison to label-free LRSPR. However, the benefit of AuNP tag signal amplification approaches was found to be greater for cSPR than for LRSPR.
机译:金纳米颗粒(AuNP)分子标签在基于SPR的免疫测定中产生了明显的信号增强。尽管已经对AuNP标签的结构功能进行了详尽的研究,但e逝场强度和分布的作用仍有待阐明。与传统的SPR(cSPR)相比,远距离表面等离子体共振(LRSPR)具有更大的磁场和更长的穿透深度。我们在这里报告了使用有限元方法建立的理论模拟和实验测量值对AuNP标签LRSPR信号增强免疫测定的优化。然后使用模型三明治免疫测定法检测癌胚抗原(CEA),以证明AuNP标签增强LRSPR的可行性。实验测量与理论模型非常吻合,与无标记的LRSPR相比,使用50 nm AuNP标签可获得高达50倍的灵敏度提高。但是,发现cSPR的AuNP标签信号放大方法的益处大于LRSPR的益处。

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