Electrochemical Sensors Based on MoSx‐Functionalized Laser‐Induced Graphene for Real‐Time Monitoring of Phenazines Produced by Pseudomonas aeruginosa

绿脓素 铜绿假单胞菌 吩嗪 石墨烯 检出限 生物膜 材料科学 电化学气体传感器 纳米技术 组合化学 电化学 化学 细菌 生物 生物化学 群体感应 色谱法 电极 遗传学 物理化学
作者
Keren Zhou,Vinay Kammarchedu,Derrick Butler,Pouya Soltan Khamsi,Aida Ebrahimi
出处
期刊:Advanced Healthcare Materials [Wiley]
卷期号:11 (19) 被引量:4
标识
DOI:10.1002/adhm.202200773
摘要

Pseudomonas aeruginosa (P. aeruginosa) is an opportunistic pathogen causing infections in blood and implanted devices. Traditional identification methods take more than 24 h to produce results. Molecular biology methods expedite detection, but require an advanced skill set. To address these challenges, this work demonstrates functionalization of laser-induced graphene (LIG) for developing flexible electrochemical sensors for P. aeruginosa based on phenazines. Electrodeposition as a facile approach is used to functionalize LIG with molybdenum polysulfide (MoSx ). The sensor's limit of detection (LOD), sensitivity, and specificity are determined in broth, agar, and wound simulating medium (WSM). Control experiments with Escherichia coli, which does not produce phenazines, demonstrate specificity of sensors for P. aeruginosa. The LOD for pyocyanin (PYO) and phenazine-1-carboxylic acid (PCA) is 0.19 × 10-6 and 1.2 × 10-6 m, respectively. Furthermore, the highly stable sensors enable real-time monitoring of P. aeruginosa biofilms over several days. Comparing square wave voltammetry data over time shows time-dependent generation of phenazines. In particular, two configurations-"Normal" and "Flipped"-are studied, showing that the phenazines time dynamics vary depending on how cells interact with sensors. The reported results demonstrate the potential of the developed sensors for integration with wound dressings for early diagnosis of P. aeruginosa infection.

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