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首页> 外文期刊>Lab on a chip >Nanotextured superhydrophobic electrodes enable detection of attomolar-scale DNA concentration within a droplet by non-faradaic impedance spectroscopy
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Nanotextured superhydrophobic electrodes enable detection of attomolar-scale DNA concentration within a droplet by non-faradaic impedance spectroscopy

机译:纳米结构的超疏水电极可通过非法拉第阻抗光谱法检测液滴中的摩尔摩尔浓度的DNA浓度

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Label-free, rapid detection of biomolecules in microliter volumes of highly diluted solutions (sub-femtomolar) is of essential importance for numerous applications in medical diagnostics, food safety, and chem-bio sensing for homeland security. At ultra-low concentrations, regardless of the sensitivity of the detection approach, the sensor response time is limited by physical diffusion of molecules towards the sensor surface. We have developed a fast, low cost, non-faradaic impedance sensing method for detection of synthetic DNA molecules in Dl water at attomolar levels by beating the diffusion limit through evaporation of a micro-liter droplet of DNA on a nanotextured superhydrophobic electrode array. Continuous monitoring of the impedance of individual droplets as a function of evaporation time is exploited to dramatically improve the sensitivity and robustness of detection. Formation of the nanostructures on the electrode surface not only increases the surface hydrophobicity, but also allows robust pinning of the droplet contact area to the sensor surface. These two features are critical for performing highly stable impedance measurements as the droplet evaporates. Using this scheme, the detection limit of conventional non-faradaic methods is improved by five orders of magnitude. The proposed platform represents a step-forward towards realization of ultra-sensitive lab-on-chip biomolecule detectors for real time point-of-care application. Further works are however needed to ultimately realize the full potential of the proposed approach to appraise biological samples in complex buffer solutions rather than in Dl water.
机译:在微升量的高稀释溶液(亚飞摩尔)中,无标签,快速检测生物分子对于医疗诊断,食品安全和国土安全的化学生物传感中的众多应用至关重要。在超低浓度下,无论检测方法的灵敏度如何,传感器响应时间都受到分子向传感器表面的物理扩散的限制。我们已经开发了一种快速,低成本,非法拉第阻抗感测方法,用于通过在纳米纹理化的超疏水电极阵列上蒸发一微升DNA液滴来克服扩散极限,从而以摩尔浓度检测去离子水中的合成DNA分子。连续监测各个液滴的阻抗随蒸发时间的变化,可显着提高检测的灵敏度和鲁棒性。在电极表面上形成纳米结构不仅增加了表面疏水性,而且还允许将液滴接触区域牢固地钉扎到传感器表面。这两个功能对于在液滴蒸发时执行高度稳定的阻抗测量至关重要。使用此方案,常规非法拉第方法的检测极限提高了五个数量级。所提出的平台代表了朝着实时护理点应用的超灵敏芯片实验室生物分子检测器迈进的一步。然而,需要进一步的工作来最终实现所提出的方法的全部潜力,以评估复杂缓冲溶液而不是去离子水中的生物样品。

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