Department of Biomedical Engineering, University of Cincinnati, Cincinnati, Ohio 45221, United States.
Medical Scientist Training Program, University of Cincinnati College of Medicine, Cincinnati, Ohio 45267, United States.
ACS Sens. 2023 Mar 24;8(3):1119-1131. doi: 10.1021/acssensors.2c02403. Epub 2023 Mar 8.
Conventional wisdom suggests that widely utilized self-assembled alkylthiolate monolayers on gold are too unstable to last more than several days when exposed to complex fluids such as raw serum at body temperature. Demonstrated here is that these monolayers can not only last at least 1 week under such harsh conditions but that significant applied value can be captured for continuous electrochemical aptamer biosensors. Electrochemical aptamer biosensors provide an ideal tool to investigate monolayer degradation, as aptamer sensors require a tightly packed monolayer to preserve sensor signal vs background current and readily reveal fouling by albumin and other solutes when operating in biofluids. Week-long operation in serum at 37 °C is achieved by (1) increasing van der Waals interactions between adjacent monolayer molecules to increase the activation energy required for desorption, (2) optimizing electrochemical measurement to decrease both alkylthiolate oxidation and electric-field-induced desorption, and (3) mitigating fouling using protective zwitterionic membranes and zwitterion-based blocking layers with antifouling properties. This work further proposes origins and mechanisms of monolayer degradation in a logical stepwise manner that was previously unobservable over multiday time scales. Several of the observed results are surprising, revealing that short-term improvements to sensor longevity (i.e., hours) actually increase sensor degradation in the longer term (i.e., days). The results and underlying insights on mechanisms not only push forward fundamental understanding of stability for self-assembled monolayers but also demonstrate an important milestone for continuous electrochemical aptamer biosensors.
传统观点认为,在金表面广泛应用的自组装烷基硫醇单层在复杂流体(如体温下的原始血清)中非常不稳定,只能持续几天。本文证明,在如此恶劣的条件下,这些单层不仅可以持续至少 1 周,而且可以为连续电化学适体生物传感器捕获重要的应用价值。电化学适体生物传感器为研究单层降解提供了理想的工具,因为适体传感器需要紧密包装的单层来保持传感器信号与背景电流的比值,并在生物流体中操作时容易发现白蛋白和其他溶质的污染。通过以下三种方法在 37°C 的血清中实现长达 1 周的运行:(1)增加相邻单层分子之间的范德华相互作用,以增加解吸所需的活化能;(2)优化电化学测量,以减少烷基硫醇的氧化和电场诱导的解吸;(3)使用具有抗污染性能的保护性两性离子膜和两性离子基阻挡层来减轻污染。这项工作进一步以逻辑的逐步方式提出了单层降解的起源和机制,这在以前的多日时间尺度上是无法观察到的。一些观察到的结果令人惊讶,表明传感器寿命的短期改善(即数小时)实际上会在更长时间内(即数天)增加传感器的降解。这些结果和对机制的深入了解不仅推动了自组装单层稳定性的基础理解,而且还展示了连续电化学适体生物传感器的重要里程碑。