采用片上 DEP 辅助传感技术的多功能 CMOS 生物传感器阵列,无需外部电极即可实现低浓度分析物的快速检测和闭环粒子操纵。

Dongwon Lee;Doohwan Jung;Fuze Jiang;Gregory Villiam Junek;Jongseok Park;Hangxing Liu;Ying Kong;Adam Wang;Youngin Kim;Kyung-Sik Choi;Jing Wang;Hua Wang
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摘要

本文介绍了一种全集成的介电泳(DEP)辅助多功能 CMOS 生物传感器阵列芯片,该芯片包含 4096 个工作电极(WE)、12288 个光电二极管(PD)、参比电极(RE)和对电极(CE),每个工作电极和光电二极管均可重新配置,以支持片上 DEP 驱动、电化学恒电位仪、光影成像和复合阻抗传感。所提出的 CMOS 生物传感器是用于快速检测低浓度分析物的致动辅助无标记生物传感器的范例。拟议的 CMOS 生物传感器的 DEP 驱动器不需要任何外部电极。相反,片上 WE 对可重复用于 DEP 驱动,从而简化传感器阵列设计。CMOS 生物传感器采用标准 130 纳米 BiCMOS 工艺实现。作为概念验证,对片上 DEP 操作进行了理论分析和有限元法(FEM)模拟。用大肠杆菌和微珠(光学阴影成像)进行的生物检测测量(DEP 驱动/电化学恒电位仪/阻抗传感)证明了低浓度分析物的快速检测以及大颗粒的同步操作和检测。片上 DEP 操作使分析物更接近传感器电极表面,从而克服了扩散极限,加速了低浓度分析物的传感。此外,片上光电二极管阵列可随时检测基于 DEP 技术的大颗粒移动,从而实现颗粒和液滴的闭环控制和传感。这些都显示了 DEP 辅助多功能生物传感器的独特优势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Multi-Functional CMOS Biosensor Array With On-Chip DEP-Assisted Sensing for Rapid Low-Concentration Analyte Detection and Close-Loop Particle Manipulation With No External Electrodes
This article presents a fully-integrated dielectrophoresis (DEP)-assisted multi-functional CMOS biosensor array chip with 4096 working electrodes (WEs), 12288 photodiodes (PDs), reference electrodes (REs), and counter electrodes (CEs), while each WE and photodiode can be reconfigured to support on-chip DEP actuation, electrochemical potentiostat, optical shadow imaging, and complex impedance sensing. The proposed CMOS biosensor is an example of an actuation-assisted label-free biosensor for the rapid sensing of low-concentration analytes. The DEP actuator of the proposed CMOS biosensor does not require any external electrode. Instead, on-chip WE pairs can be re-used for DEP actuation to simplify the sensor array design. The CMOS biosensor is implemented in a standard 130-nm BiCMOS process. Theoretical analyses and finite element method (FEM) simulations of the on-chip DEP operations are conducted as proof of concept. Biological assay measurements (DEP actuation/electrochemical potentiostat/impedance sensing) with E.coli bacteria and microbeads (optical shadow imaging) demonstrate rapid detection of low-concentration analytes and simultaneous manipulation and detection of large particles. The on-chip DEP operations draw the analytes closer to the sensor electrode surface, which overcomes the diffusion limit and accelerates low-concentration analyte sensing. Moreover, the DEP-based movement of large particles can be readily detected by on-chip photodiode arrays to achieve close-loop manipulation and sensing of particles and droplets. These show the unique advantages of the DEP-assisted multi-functional biosensor.
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