Fabrication of fluidic-based memristor sensor for dengue virus detection

N. Hadis, A. A. Manaf, S. H. Ngalim, S. H. Herman, K. Sawada, N. A. Fauzi
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引用次数: 7

Abstract

In this paper, the implementation of fluidic-based memristor sensor in bio-sensing application is presented. The sensor was fabricated using sol-gel spin coating technique and chemically-modified with antidengue virus NS1 glycoprotein monoclonal antibody before being presented with its ligand, NS1 glycoprotein. Four different concentrations of NS1 glycoprotein (52 nM, 104 nM, 208 nM and 416 nM) were tested on the modified sensor. Each sensor has nine wells, which function to increase the binding area for trapping more viral proteins. To test whether the efficiency of the sensor is attributed by the surface area of each well, four different diameters of the well were fabricated: 0.5 mm, 1 mm, 1.5 mm and 2 mm. These sensors were characterized using field emission scanning electron microscope (FESEM) and semiconductor characterization system (current-voltage (I-V)). FESEM images of the wells show different surface morphologies prior to biochemical treatment, after the bound-antibody modification and after the presentation of viral protein. Off-on resistance ratio extracted from I-V curve between the antibody-bound sensor with and without the viral protein. Analysis shows that the loop area increases as the NS1 glycoprotein applied to the modified sensor. The area within the loop also increases as the concentration of the NS1 glycoprotein increases. The most significant change in loop area is observed upon introduction of 416 nM. Memristor sensor with 2 mm-well diameter recorded the highest sensitivity when compared to the other three well diameters. The recorded sensitivity for the 2 mm-well diameter is 6.53 × 10−3 nM−1 according to fluidic-based platform. These findings conclude that specific-binding between dengue virus antibody and NS1 glycoprotein of dengue virus can be detected by the sensor via the change in electrical conductivity.
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登革病毒检测用流体型忆阻传感器的研制
本文介绍了基于流体的忆阻器传感器在生物传感中的应用。该传感器采用溶胶-凝胶自旋包衣技术制备,用抗登革病毒NS1糖蛋白单克隆抗体对其进行化学修饰,然后将其配体NS1糖蛋白呈递。在改进的传感器上检测了4种不同浓度的NS1糖蛋白(52 nM、104 nM、208 nM和416 nM)。每个传感器有九个孔,其功能是增加结合区域,以捕获更多的病毒蛋白质。为了测试传感器的效率是否与每口井的表面积有关,我们制作了四种不同直径的井:0.5 mm、1mm、1.5 mm和2mm。利用场发射扫描电镜(FESEM)和半导体表征系统(电流-电压(I-V))对传感器进行了表征。在生化处理前、结合抗体修饰后和病毒蛋白呈递后,孔的FESEM图像显示出不同的表面形态。从带病毒蛋白和不带病毒蛋白的抗体结合传感器之间的I-V曲线提取开关电阻比。分析表明,随着NS1糖蛋白的加入,传感器的环路面积增加。环内的面积也随着NS1糖蛋白浓度的增加而增加。在引入416 nM时观察到环路面积的最显著变化。与其他三种井径相比,直径为2mm的忆阻器传感器的灵敏度最高。根据流体平台,记录的2 mm井径的灵敏度为6.53 × 10−3 nM−1。这些结果表明,该传感器可以通过电导率的变化检测登革病毒抗体与登革病毒NS1糖蛋白的特异性结合。
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