适体
介电谱
校准
电极
电阻抗
材料科学
生物传感器
分析化学(期刊)
信号(编程语言)
化学
分辨率(逻辑)
生物系统
电化学
纳米技术
计算机科学
色谱法
人工智能
电气工程
物理
遗传学
物理化学
量子力学
生物
程序设计语言
工程类
作者
Brian Roehrich,Kaylyn K. Leung,Julian Gerson,Tod E. Kippin,Kevin W. Plaxco,Lior Sepunaru
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2023-08-16
卷期号:8 (8): 3051-3059
被引量:19
标识
DOI:10.1021/acssensors.3c00632
摘要
Electrochemical aptamer-based (EAB) sensors are capable of measuring the concentrations of specific molecules in vivo, in real time, and with a few-second time resolution. For their signal transduction mechanism, these sensors utilize a binding-induced conformational change in their target-recognizing, redox-reporter-modified aptamer to alter the rate of electron transfer between the reporter and the supporting electrode. While a variety of voltammetric techniques have been used to monitor this change in kinetics, they suffer from various drawbacks, including time resolution limited to several seconds and sensor-to-sensor variation that requires calibration to remove. Here, however, we show that the use of fast Fourier transform electrochemical impedance spectroscopy (FFT-EIS) to interrogate EAB sensors leads to improved (here better than 2 s) time resolution and calibration-free operation, even when such sensors are deployed in vivo. To showcase these benefits, we demonstrate the approach's ability to perform real-time molecular measurements in the veins of living rats.
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