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Determination of brain injury biomarkers by surface-enhanced Raman scattering using hollow gold nanospheres

机译:用中空金纳米球表面增强拉曼散射测定脑损伤生物标志物

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摘要

The development of rapid, highly sensitive detection methods for neuron-specific enolase (NSE) and S100-beta protein is very important as the levels of NSE and S100-beta protein in the blood are closely related to brain injury. Therefore, we can use NSE and S100-beta protein concentration detection to realize the preliminary judgment of brain injury. In this paper, we report that a simple label-free three dimensional hierarchical plasmonic nano-architecture has been designed for the sensitive surface-enhanced Raman scattering immunosensor detection of NSE and S100-beta. Owing to the active group of the hollow gold nanospheres (HAuNPs), the redox molecules 4-mercaptobenzoic acid (4-MBA) and Nile blue A (NBA) absorb antibodies and provide signal generation. The prepared HAuNPs@4-MBA and HAuNPs@NBA are used as probes to easily construct a surface-enhanced Raman scattering immunosensor. When protein biomarkers are present, the sandwich nanoparticles are captured over the substrate, forming a confined plasmonic field, leading to an enhanced electromagnetic field in intensity and in space. As a result, the Raman reporter molecules are exposed to a high density of "hot spots", which remarkably amplify the Raman signal, improving the sensitivity of the surface-enhanced Raman scattering immunosensor. Under the optimized conditions, the linear range of the proposed immunosensor is from 0.2 to 22 ng mL(-1) for both NSE and S100-beta. The lowest detectable concentration is 0.1 and 0.06 ng mL(-1) for NSE and S100-beta, respectively. The assay results for serum samples with the proposed method were in a good agreement with the standard enzyme-linked immunosorbent assay method. The proposed immunosensor is promising in clinical diagnosis. This method, which utilizes the surface-enhanced Raman scattering of HAuNPs, has great potential in the detection of biomarkers, which are vital in medical diagnoses and disease monitoring.
机译:作为神经元特异性烯醇酶(NSE)和S100-β蛋白的快速,高灵敏度检测方法的发展非常重要,因为血液中的NSE和S100-β蛋白水平与脑损伤密切相关。因此,我们可以使用NSE和S100-β蛋白浓度检测来实现脑损伤的初步判断。在本文中,我们报告说明了一个简单的无标签三维分层等离子体纳米架构专为敏感的表面增强拉曼散射免疫传感器检测NSE和S100-β。由于中空金纳米球(Haunps)的活性组,氧化还原分子4-巯基苯甲酸(4-MBA)和尼罗蓝色A(NBA)吸收抗体并提供信号产生。制备的Haunps @ 4-MBA和Haunps @ NBA用作探针,以容易地构建表面增强的拉曼散射免疫传感器。当存在蛋白质生物标志物时,将夹层纳米颗粒捕获在基板上,形成狭窄的等离子体场,导致强度和空间中的增强的电磁场。结果,拉曼报告器分子暴露于高密度的“热点”,其显着放大拉曼信号,从而提高了表面增强拉曼散射免疫传感器的灵敏度。在优化条件下,所提出的免疫传感器的线性范围为NSE和S100-β的0.2至22ng ml(-1)。对于NSE和S100-Beta,最低可检测浓度为0.1和0.06 ng(-1)。具有该方法的血清样品的测定结果与标准酶联免疫吸附测定法吻合良好。拟议的免疫传感器在临床诊断中具有很有希望。这种利用Haunps的表面增强拉曼散射的这种方法具有很大的潜力在医学诊断和疾病监测中至关重要。

著录项

  • 来源
    《RSC Advances》 |2018年第6期|共8页
  • 作者单位

    Southeast Univ Sch Biol Sci &

    Med Engn State Key Lab Bioelect Nanjing 210096 Jiangsu Peoples R China;

    Southeast Univ Sch Biol Sci &

    Med Engn State Key Lab Bioelect Nanjing 210096 Jiangsu Peoples R China;

    Taishan Med Univ Life Sci Res Ctr Key Lab Cerebral Microcirculat Univ Shandong Taishan 271016 Peoples R China;

    Taishan Med Univ Life Sci Res Ctr Key Lab Cerebral Microcirculat Univ Shandong Taishan 271016 Peoples R China;

    Taishan Med Univ Life Sci Res Ctr Key Lab Cerebral Microcirculat Univ Shandong Taishan 271016 Peoples R China;

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  • 正文语种 eng
  • 中图分类 化学;
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