首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >Dual signal amplification of surface plasmon resonance imaging for sensitive immunoassay of tumor marker
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Dual signal amplification of surface plasmon resonance imaging for sensitive immunoassay of tumor marker

机译:表面等离子体共振成像的双信号放大,用于肿瘤标记物的敏感免疫测定

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摘要

Surface plasmon resonance imaging (SPRi) is an intriguing technique for immunoassay with the inherent advantages of being high throughput, real time, and label free, but its sensitivity needs essential improvement for practical applications. Here, we report a dual signal amplification strategy using functional gold nanoparticles (AuNPs) followed by on-chip atom transfer radical polymerization (ATRP) for sensitive SPRi immunoassay of tumor biomarker in human serum. The AuNPs are grafted with an initiator of ATRP as well as a recognition antibody, where the antibody directs the specific binding of functional AuNPs onto the SPRi sensing surface to form immunocomplexes for first signal amplification and the initiator allows for on-chip ATRP of 2-hydroxyethyl methacrylate (HEMA) from the AuNPs to further enhance the SPRi signal. High sensitivity and broad dynamic range are achieved with this dual signal amplification strategy for detection of a model tumor marker, α-fetoprotein (AFP), in 10% human serum.
机译:表面等离子体共振成像(SPRi)是一种免疫分析技术,具有高通量,实时和无标记的固有优势,但其灵敏度需要在实际应用中进行重大改进。在这里,我们报告了双重信号放大策略,使用功能性金纳米颗粒(AuNPs),然后使用片上原子转移自由基聚合(ATRP)进行人类血清中肿瘤生物标记物的灵敏SPRi免疫测定。 AuNPs与ATRP的引发剂和识别抗体移植在一起,其中该抗体将功能性AuNPs特异性结合到SPRi传感表面上,形成免疫复合物,用于第一次信号放大,并且引发剂允许2-的芯片上ATRP。来自AuNP的甲基丙烯酸羟乙酯(HEMA)可进一步增强SPRi信号。通过这种双重信号放大策略,可以在10%的人血清中检测模型肿瘤标志物α-甲胎蛋白(AFP),从而实现了高灵敏度和宽动态范围。

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