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Attomole Sensitivity of Staphylococcal Enterotoxin B Detection Using an Aptamer-Modified Surface-Enhanced Raman Scattering Probe

机译:使用适体修饰的表面增强拉曼散射探针检测葡萄球菌肠毒素B的原子敏感性

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摘要

In this report, we present a new homogeneous detection method for staphylococcal enterotoxin B (SEB) utilizing core-shell-structured iron-gold magnetic nanoparticles and a gold nanorod surface-enhanced Raman scattering (SERS) probe in solution. Peptide ligand (aptamer) functionalized magnetic gold nanorod particles were used as scavengers for target SEB. After the SEB molecules were separated from the matrix, the sandwich assay procedure was tested by gold nanorod particles that act as SERS probes. The binding constant between SEB and peptide-nanoparticle complex was determined as 8.0 × 10~7 M~(-1). The correlation between the SEB concentration and SERS signal was found to be linear within the range of 2.5 fM to 3.2 nM. The limit of detection for the homogeneous assay was determined as 224 aM (ca. 2697 SEB molecules/20 μL sample volume). Also, gold-coated surfaces were used as capture substrates and performances of the two methods were compared. Furthermore, the developed method was evaluated for investigating the SEB specificity on bovine serum albumin (BSA) and avidin and detecting SEB in artificially contaminated milk, blood, and urine.
机译:在此报告中,我们提出了一种新的均相检测方法,用于利用溶液中的核-壳结构铁金磁性纳米粒子和金纳米棒表面增强拉曼散射(SERS)探针对葡萄球菌肠毒素B(SEB)进行检测。肽配体(适体)功能化的磁性金纳米棒颗粒用作目标SEB的清除剂。从基质中分离出SEB分子后,通过金纳米棒颗粒(用作SERS探针)测试了夹心测定法。 SEB与肽-纳米颗粒复合物之间的结合常数确定为8.0×10〜7 M〜(-1)。发现SEB浓度和SERS信号之间的相关在2.5 fM至3.2 nM的范围内呈线性关系。均相测定的检测下限确定为224 aM(约2697 SEB分子/ 20μL样品体积)。另外,将镀金表面用作捕获基底,并比较了两种方法的性能。此外,对开发的方法进行了评估,以调查SEB对牛血清白蛋白(BSA)和抗生物素蛋白的特异性,并检测人为污染的牛奶,血液和尿液中的SEB。

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