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激光诱导的石墨烯叉指电极用于无标记或纳米标记增强的基于高灵敏度电容适配体的生物传感器。

Laser-induced graphene interdigitated electrodes for label-free or nanolabel-enhanced highly sensitive capacitive aptamer-based biosensors.

机构信息

Institute of Analytical Chemistry, Chemo-and Biosensors, Faculty of Chemistry and Pharmacy, University of Regensburg, 31, 93053, Regensburg, Germany; School of Integrative Engineering, Chung-Ang University, Heukseok-dong, Dongjak-Gu, 06974, Seoul, Republic of Korea.

Institute of Analytical Chemistry, Chemo-and Biosensors, Faculty of Chemistry and Pharmacy, University of Regensburg, 31, 93053, Regensburg, Germany.

出版信息

Biosens Bioelectron. 2020 Sep 15;164:112272. doi: 10.1016/j.bios.2020.112272. Epub 2020 May 21.

Abstract

Highly porous laser-induced graphene (LIG) is easily generated in complex electrode configurations such as interdigitated electrodes (IDEs). Here, we demonstrate that their superior capacitive response at low frequencies can be exploited in affinity biosensors using thrombin aptamers as model biorecognition elements. Of specific interest was the effect of electrode surface area on capacitance detection, and the comparison between a label-free format and enhancement strategies afforded by carboxy group bearing polymeric nanoparticles or liposomes. Electrochemical impedance spectroscopy (EIS) was used to investigate the LIG performance and optimize the biosensor design. Interestingly, the label-free strategy performed extremely well and additional labels decreased the limit of detection or increased the sensitivity only minimally. It is assumed that the highly porous nature of the LIG structures dominates the capacitive response so that labels removed from the surface have only limited influence Also, while slight performance changes can be observed for smaller vs. larger electrode structures, the performance of a LIG IDE is reasonably independent of its size. In the end, a dynamic range of 5 orders of magnitude was obtained (0.01 nM-1000 nM) with a limit of detection as low as 0.12 pM. When measured in serum, this increased to 1.3 pM. The good reproducibility (relative standard deviation (RSD), 4.90%) and repeatability (RSD, 2.59%) and good long-term stability (>7 weeks at 4 °C) prove that a LIG-based capacitance sensor is an excellent choice for affinity-based biosensor. The ease-of-production, the simplicity of modification and the superior performance even in a label-free format indicate that LIG-based biosensors should be considered in point-of-care diagnostics in the future.

摘要

高度多孔的激光诱导石墨烯(LIG)很容易在复杂的电极结构中生成,例如叉指电极(IDE)。在这里,我们证明了它们在低频下的卓越电容响应可以在亲和生物传感器中得到利用,使用凝血酶适体作为模型生物识别元件。特别感兴趣的是电极表面积对电容检测的影响,以及无标记格式与带羧基的聚合物纳米粒子或脂质体提供的增强策略之间的比较。电化学阻抗谱(EIS)用于研究 LIG 性能并优化生物传感器设计。有趣的是,无标记策略表现非常出色,额外的标签仅略微降低了检测限或提高了灵敏度。据推测,LIG 结构的高度多孔性质主导了电容响应,因此从表面去除的标签只有有限的影响。此外,虽然较小 vs. 较大的电极结构可以观察到轻微的性能变化,但 LIG IDE 的性能相当独立于其尺寸。最终,获得了 5 个数量级的动态范围(0.01 nM-1000 nM),检测限低至 0.12 pM。当在血清中测量时,这个值增加到 1.3 pM。良好的重现性(相对标准偏差(RSD),4.90%)和重复性(RSD,2.59%)以及良好的长期稳定性(>7 周在 4°C)证明,基于 LIG 的电容传感器是亲和生物传感器的绝佳选择。生产简单、修饰简单且即使在无标记格式下也具有卓越的性能表明,基于 LIG 的生物传感器在未来应考虑用于即时诊断。

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