Center for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), Paseo de Miramón 194, 20014, Donostia-San Sebastián, Spain.
University of the Basque Country, UPV-EHU, 20018 San Sebastián, Spain.
Nanoscale. 2023 Oct 26;15(41):16650-16657. doi: 10.1039/d3nr04153k.
In the last decade, solution-gated graphene field effect transistors (GFETs) showed their versatility in the development of a miniaturized multiplexed platform for electrophysiological recordings and sensing. Due to their working mechanism, the surface functionalisation and immobilisation of receptors are pivotal to ensure the proper functioning of devices. Herein, we present a controlled covalent functionalisation strategy based on molecular design and electrochemical triggering, which provide a monolayer-like functionalisation of micro-GFET arrays retaining the electronic properties of graphenes. The functionalisation layer as a receptor was then employed as the linker for serotonin aptamer conjugation. The micro-GFET arrays display sensitivity toward the target analyte in the micromolar range in a physiological buffer (PBS 10 mM). The sensor allows the in-flow real-time monitoring of serotonin transient concentrations with fast and reversible responses.
在过去的十年中,基于溶液的石墨烯场效应晶体管(GFET)在开发用于电生理记录和传感的小型化多路复用平台方面显示出了多功能性。由于其工作机制,受体的表面功能化和固定化对于确保器件的正常运行至关重要。在此,我们提出了一种基于分子设计和电化学触发的受控共价功能化策略,该策略为微 GFET 阵列提供了类似于单层的功能化,同时保留了石墨烯的电子特性。然后,将功能化层作为受体用于与血清素适体的连接。在生理缓冲液(10 mM PBS)中,微 GFET 阵列对目标分析物在微摩尔范围内表现出敏感性。该传感器允许实时监测血清素瞬态浓度,并具有快速和可逆的响应。