Xian Minghan, Luo Hao, Xia Xinyi, Fares Chaker, Carey Patrick H, Chiu Chan-Wen, Ren Fan, Shan Siang-Sin, Liao Yu-Te, Hsu Shu-Min, Esquivel-Upshaw Josephine F, Chang Chin-Wei, Lin Jenshan, Ghivizzani Steven C, Pearton Stephen J
Department of Chemical Engineering, University of Florida, Gainesville, Florida 32611.
Department of Electrical and Computer Engineering, National Chiao Tung University, Hsinchu 30010, Taiwan.
J Vac Sci Technol B Nanotechnol Microelectron. 2021 May;39(3):033202. doi: 10.1116/6.0001060. Epub 2021 May 18.
Detection of the SARS-CoV-2 spike protein and inactivated virus was achieved using disposable and biofunctionalized functional strips, which can be connected externally to a reusable printed circuit board for signal amplification with an embedded metal-oxide-semiconductor field-effect transistor (MOSFET). A series of chemical reactions was performed to immobilize both a monoclonal antibody and a polyclonal antibody onto the Au-plated electrode used as the sensing surface. An important step in the biofunctionalization, namely, the formation of Au-plated clusters on the sensor strips, was verified by scanning electron microscopy, as well as electrical measurements, to confirm successful binding of thiol groups on this Au surface. The functionalized sensor was externally connected to the gate electrode of the MOSFET, and synchronous pulses were applied to both the sensing strip and the drain contact of the MOSFET. The resulting changes in the dynamics of drain waveforms were converted into analog voltages and digital readouts, which correlate with the concentration of proteins and virus present in the tested solution. A broad range of protein concentrations from 1 fg/ml to 10 g/ml and virus concentrations from 100 to 2500 PFU/ml were detectable for the sensor functionalized with both antibodies. The results show the potential of this approach for the development of a portable, low-cost, and disposable cartridge sensor system for point-of-care detection of viral diseases.
使用一次性且经过生物功能化处理的功能条实现了对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)刺突蛋白和灭活病毒的检测,该功能条可外部连接至一个带有嵌入式金属氧化物半导体场效应晶体管(MOSFET)的可重复使用印刷电路板以进行信号放大。进行了一系列化学反应,将单克隆抗体和多克隆抗体固定在用作传感表面的镀金电极上。通过扫描电子显微镜以及电学测量对生物功能化过程中的一个重要步骤,即在传感器条上形成镀金簇进行了验证,以确认硫醇基团在该金表面的成功结合。将功能化的传感器外部连接至MOSFET的栅极电极,并对传感条和MOSFET的漏极触点施加同步脉冲。漏极波形动态变化所产生的结果被转换为模拟电压和数字读数,这些读数与测试溶液中存在的蛋白质和病毒浓度相关。对于用两种抗体功能化的传感器,可检测到1 fg/ml至10 g/ml的广泛蛋白质浓度范围以及100至2500 PFU/ml的病毒浓度范围。结果显示了这种方法在开发用于即时检测病毒疾病的便携式、低成本且一次性的盒式传感器系统方面的潜力。