Institute of Bioelectronics (PGI-8/ICS-8), Forschungszentrum Jülich , 52425 Jülich, Germany.
Neuroelectronics, IMETUM, Department of Electrical and Computer Engineering, Technical University of Munich , Boltzmannstr. 11, 85748 Garching, Germany.
Acc Chem Res. 2016 Sep 20;49(9):2031-40. doi: 10.1021/acs.accounts.6b00333. Epub 2016 Sep 7.
Micro- and nanofabriation technologies have a tremendous potential for the development of powerful sensor array platforms for electrochemical detection. The ability to integrate electrochemical sensor arrays with microfluidic devices nowadays provides possibilities for advanced lab-on-a-chip technology for the detection or quantification of multiple targets in a high-throughput approach. In particular, this is interesting for applications outside of analytical laboratories, such as point-of-care (POC) or on-site water screening where cost, measurement time, and the size of individual sensor devices are important factors to be considered. In addition, electrochemical sensor arrays can monitor biological processes in emerging cell-analysis platforms. Here, recent progress in the design of disease model systems and organ-on-a-chip technologies still needs to be matched by appropriate functionalities for application of external stimuli and read-out of cellular activity in long-term experiments. Preferably, data can be gathered not only at a singular location but at different spatial scales across a whole cell network, calling for new sensor array technologies. In this Account, we describe the evolution of chip-based nanoscale electrochemical sensor arrays, which have been developed and investigated in our group. Focusing on design and fabrication strategies that facilitate applications for the investigation of cellular networks, we emphasize the sensing of redox-active neurotransmitters on a chip. To this end, we address the impact of the device architecture on sensitivity, selectivity as well as on spatial and temporal resolution. Specifically, we highlight recent work on redox-cycling concepts using nanocavity sensor arrays, which provide an efficient amplification strategy for spatiotemporal detection of redox-active molecules. As redox-cycling electrochemistry critically depends on the ability to miniaturize and integrate closely spaced electrode systems, the fabrication of suitable nanoscale devices is of utmost importance for the development of this advanced sensor technology. Here, we address current challenges and limitations, which are associated with different redox cycling sensor array concepts and fabrication approaches. State-of-the-art micro- and nanofabrication technologies based on optical and electron-beam lithography allow precise control of the device layout and have led to a new generation of electrochemical sensor architectures for highly sensitive detection. Yet, these approaches are often expensive and limited to clean-room compatible materials. In consequence, they lack possibilities for upscaling to high-throughput fabrication at moderate costs. In this respect, self-assembly techniques can open new routes for electrochemical sensor design. This is true in particular for nanoporous redox cycling sensor arrays that have been developed in recent years and provide interesting alternatives to clean-room fabricated nanofluidic redox cycling devices. We conclude this Account with a discussion of emerging fabrication technologies based on printed electronics that we believe have the potential of transforming current redox cycling concepts from laboratory tools for fundamental studies and proof-of-principle analytical demonstrations into high-throughput devices for rapid screening applications.
微纳制造技术在开发用于电化学检测的强大传感器阵列平台方面具有巨大的潜力。如今,将电化学传感器阵列与微流控器件集成的能力为先进的微流控技术提供了可能,可用于高通量方法中对多个目标的检测或定量。特别是,这对于分析实验室以外的应用很有意义,例如即时护理 (POC) 或现场水筛选,其中成本、测量时间和单个传感器设备的尺寸是需要考虑的重要因素。此外,电化学传感器阵列可在新兴的细胞分析平台中监测生物过程。在这里,疾病模型系统和类器官芯片技术的最新进展仍然需要与外部刺激的应用和长期实验中细胞活性的读出等适当功能相匹配。最好不仅可以在单个位置收集数据,还可以在整个细胞网络的不同空间尺度上收集数据,这需要新的传感器阵列技术。在本专题介绍中,我们描述了我们小组开发和研究的基于芯片的纳米级电化学传感器阵列的发展。重点介绍了有利于细胞网络研究应用的设计和制造策略,我们强调了在芯片上检测氧化还原活性神经递质。为此,我们讨论了器件结构对灵敏度、选择性以及空间和时间分辨率的影响。具体来说,我们强调了使用纳米腔传感器阵列的氧化还原循环概念的最新工作,该概念为氧化还原活性分子的时空检测提供了有效的放大策略。由于氧化还原循环电化学严重依赖于小型化和集成紧密间隔电极系统的能力,因此,对于这种先进传感器技术的发展,合适的纳米器件的制造至关重要。在这里,我们讨论了与不同的氧化还原循环传感器阵列概念和制造方法相关的当前挑战和限制。基于光学和电子束光刻的最先进的微纳制造技术可以精确控制器件布局,并为高度灵敏的检测带来新一代电化学传感器架构。然而,这些方法通常很昂贵,并且仅限于洁净室兼容的材料。因此,它们缺乏以适中的成本进行高通量制造的可能性。在这方面,自组装技术可为电化学传感器设计开辟新途径。对于近年来开发的纳米多孔氧化还原循环传感器阵列来说尤其如此,它们为洁净室制造的纳米流体氧化还原循环器件提供了有趣的替代方案。最后,我们讨论了基于印刷电子的新兴制造技术,我们相信这些技术有可能将当前的氧化还原循环概念从基础研究和原理分析演示的实验室工具转变为高通量快速筛选应用的设备。