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Silver nanoprism etching-based plasmonic ELISA for the high sensitive detection of prostate-specific antigen

机译:基于银纳米棱镜蚀刻的等离子ELISA用于前列腺特异性抗原的高灵敏度检测

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摘要

Ultrasensitive and quantitative detection using simple and low-cost assays is critical in clinical diagnostics. In this report, we developed a triangular silver nanoprism (AgNPRs) etching-based plasmonic biosensor for the detection of cancer biomarkers. The triangular AgNPRs-based plasmonic biosensor is an enzyme-linked immunosorbent assay combined with the enzyme-mediated surface plasmon resonance (SPR) of triangular AgNPRs. Triangular AgNPRs uses the immune response of prostate-specific antigen (PSA) to trigger the glucose oxidase (GOx)-catalysed oxidation of glucose (Glu), producing hydrogen peroxide. Hydrogen peroxide acts as an oxidant to etch the triangular AgNPRs into smaller spherical silver nanoparticles, which is accompanied by a substantial blueshift of the SPR peak and a colourimetric blue-to-purple change that can be observed by the naked eye. The SPR peak shift enables the quantitative assessment of PSA due to the remarkable colour change. The triangular AgNPRs-based plasmonic ELISA approach exhibited a quasilinear response to logarithmic PSA concentrations in the range of 10 fg/mL to 100 pg/mL with a limit of detection (LOD) of 4.1 fg/mL. In addition, the LOD of PSA in this approach exceeds that of the conventional HRP-based ELISA (1.25 ng/mL) approach by more than 5 orders of magnitude. Patient serum samples from 16 donors were assayed with triangular AgNPRs-based plasmonic ELISA. The results from the triangular AgNPRs-based immunoassay and the time-resolved fluorescence immunoassay showed excellent correlation, and there were no significant differences in the quantified amounts of PSA. The triangular AgNPRs-based plasmonic ELISA approach has advantages (ultrasensitive, cost-effective, ease of operation) that are expected to be of great interest in diagnostics and to be suitable for a point-of-care test. (C) 2015 Elsevier B.V. All rights reserved.
机译:使用简单且低成本的检测方法进行超灵敏和定量检测对于临床诊断至关重要。在此报告中,我们开发了一种基于三角形银纳米棱镜(AgNPR)蚀刻的等离子生物传感器,用于检测癌症生物标志物。基于三角形AgNPRs的等离子体生物传感器是与三角形AgNPRs的酶介导的表面等离振子共振(SPR)结合的酶联免疫吸附测定法。三角形AgNPR使用前列腺特异性抗原(PSA)的免疫反应来触发葡萄糖氧化酶(GOx)催化的葡萄糖氧化(Glu),产生过氧化氢。过氧化氢充当氧化剂,将三角形的AgNPR蚀刻成较小的球形银纳米颗粒,并伴有SPR峰的显着蓝移和肉眼可观察到的比色蓝紫色变化。由于显着的颜色变化,SPR峰位移使PSA的定量评估成为可能。基于三角形AgNPRs的等离子ELISA方法显示对数PSA浓度在10 fg / mL至100 pg / mL范围内的准线性响应,检出限(LOD)为4.1 fg / mL。此外,该方法中PSA的LOD超过常规基于HRP的ELISA(1.25 ng / mL)方法的LOD超过5个数量级。用基于三角形AgNPRs的等离子ELISA分析了来自16个供体的患者血清样品。基于三角形AgNPRs的免疫测定法和时间分辨荧光免疫测定法的结果显示出极好的相关性,并且PSA的定量数量没有显着差异。基于三角形AgNPRs的等离子ELISA方法具有优势(超灵敏,经济高效,易于操作),这些优势有望在诊断学中引起广泛关注,并适用于即时检验。 (C)2015 Elsevier B.V.保留所有权利。

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