Department of Chemistry, Purdue University, West Lafayette, Indiana 47906, United States.
Elmore Family School of Electrical and Computer Engineering, Purdue University, West Lafayette, Indiana 47906, United States.
ACS Sens. 2023 Mar 24;8(3):1143-1150. doi: 10.1021/acssensors.2c02427. Epub 2023 Feb 28.
With the emergence of multidrug-resistant bacteria, infection-related death toll is on the rise. Overuse of antibiotics and their leakage into waterways have transformed the environment into a sink, resulting in bacterial resistance permeating through all tiers of the food cycle. As one of the primary sources of food, fish and fish products such as fish eggs must be studied for their ability to accumulate relevant antibiotics. While the accumulation of these pharmaceuticals has previously been studied, there remains a need to analyze these processes in real time. Electrochemical aptamer-based sensor technology allows for selective, real-time monitoring of small molecules. Herein, we report the first use of miniaturized electrochemical aptamer-based sensors for the analysis of the passive uptake of the aminoglycoside antibiotic, kanamycin, in single salmon eggs. We use pulled platinum microelectrodes and increase the surface area at the electrode tip through dendritic gold deposition. These electrodes showed a 100-fold increase in DNA immobilization on the electrode surface as compared to bare microelectrodes. Additionally, the sensors showed improved stability in complex biological media over an extended period of time when compared to the more widely used macrosensors ( = 1 mm). The sensor range was determined to extend from nanomolar to micromolar concentrations of kanamycin in fish egg lysate and when used in a single salmon egg the μ-aptasensors were able to monitor the passive uptake of kanamycin over time. The accumulation kinetics were simulated using COMSOL Multiphysics software. This research presents the first reported record of passive uptake of a small molecule in a single cell in real-time using electrochemistry.
随着多药耐药菌的出现,与感染相关的死亡人数正在上升。抗生素的过度使用和它们泄漏到水道中,已经将环境变成了一个细菌耐药性的温床,导致细菌耐药性渗透到食物链的各个层面。鱼类和鱼卵等鱼类产品作为主要食物来源之一,其积累相关抗生素的能力必须加以研究。虽然之前已经研究过这些药物的积累,但仍需要实时分析这些过程。基于电化学适体的传感器技术允许对小分子进行选择性、实时监测。在这里,我们首次报道了使用小型化电化学适体传感器分析单一三文鱼卵中氨基糖苷类抗生素卡那霉素的被动摄取。我们使用拉制的铂微电极,并通过枝状金沉积增加电极尖端的表面积。与裸微电极相比,这些电极在电极表面上固定 DNA 的能力提高了 100 倍。此外,与更广泛使用的宏传感器(=1mm)相比,这些传感器在复杂的生物介质中具有更长时间的稳定性。传感器的范围确定为从纳摩尔到鱼卵裂解物中微摩尔浓度的卡那霉素,当用于单个三文鱼卵时,μ-适体传感器能够实时监测卡那霉素的被动摄取。使用 COMSOL Multiphysics 软件模拟了积累动力学。这项研究首次实时报道了使用电化学方法在单个细胞中被动摄取小分子的情况。