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首页> 外文期刊>ACS nano >Biotunable Nanoplasmonic Filter on Few-Layer MoS2 for Rapid and Highly Sensitive Cytokine Optoelectronic lmmunosensing
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Biotunable Nanoplasmonic Filter on Few-Layer MoS2 for Rapid and Highly Sensitive Cytokine Optoelectronic lmmunosensing

机译:几层MOS2上的生物填充纳米升性过滤器,用于快速且高敏感的细胞因子光电Lmmunosensing

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摘要

Monitoring of the time-varying immune status of a diseased host often requires rapid and sensitive detection of cytokines. Metallic nanoparticle-based localized surface plasmon resonance (LSPR) biosensors hold promise to meet this clinical need by permitting label-free detection of target biomolecules. These biosensors, however, continue to suffer from relatively low sensitivity as compared to conventional immunoassay methods that involve labeling processes. Their response speeds also need to be further improved to enable rapid cytokine quantification for critical care in a timely manner. In this paper, we report an immunobiosensing device integrating a biotunable nanoplasmonic optical filter and a highly sensitive few-layer molybdenum disulfide (MoS2) photoconductive component, which can serve as a generic device platform to meet the need of rapid cytokine detection with high sensitivity. The nanoplasmonic filter consists of anticytokine antibody-conjugated gold nanoparticles on a SiO2 thin layer that is placed 170 mu m above a few-layer MoS2 photoconductive flake device. The principle of the biosensor operation is based on tuning the delivery of incident light to the few-layer MoS2 photoconductive flake thorough the nanoplasmonic filter by means of biomolecular surface binding induced LSPR shifts. The tuning is dependent on cytokine concentration on the nanoplasmonic filter and optoelectronically detected by the few-layer MoS2 device. Using the developed optoelectronic biosensor, we have demonstrated label-free detection of IL-1 beta a pro-inflammatory cytokine, with a detection limit as low as 250 fg/mL (14 84), a large dynamic range of 10(6), and a short assay time of 10 min. The presented biosensing approach could be further developed and generalized for point-of-care diagnosis, wearable bio/chemical sensing, and environmental monitoring.
机译:监测患病宿主的时变免疫状况通常需要快速敏感的细胞因子。基于金属纳米粒子的局部表面等离子体共振(LSPR)生物传感器通过允许无标记的靶生物分子检测来满足该临床需求。然而,与涉及标记过程的常规免疫测定方法相比,这些生物传感器继续患有相对低的敏感性。它们还需要进一步改善它们的响应速度,以便及时地实现快速的细胞因子量化。在本文中,我们报告了一种直接聚纳米型滤光器和高敏感的少数层钼二硫化钼(MOS2)光电导器的免疫诱导装置,其可以用作通用装置平台,以满足具有高灵敏度的快速细胞因子检测。纳米升性过滤器由在SiO 2薄层上的AnticeTokine抗体缀合的金纳米颗粒组成,所述SiO 2薄层被放置170μm,在几层MOS2光电导薄片装置上方。生物传感器操作的原理是基于将入射光的递送到少数层MOS2光电导液通过生物分子表面结合诱导的LSPR偏移来调整少数层MOS2光电导液。调谐依赖于纳米升压过滤器上的细胞因子浓度并由少数层MOS2装置进行光电检测。使用开发的光电生物传感器,我们已经证明了无标记的IL-1β促炎细胞因子的检测,检测极限低至250 fg / ml(14 84),动态范围为10(6),并且短暂的测定时间为10分钟。呈现的生物腐蚀方法可以进一步开发和推广,用于护理点诊断,可穿戴生物/化学传感和环境监测。

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