化学
半胱氨酸
可穿戴计算机
接口(物质)
跟踪(教育)
纳米技术
生物化学
嵌入式系统
分子
有机化学
心理学
教育学
酶
吉布斯等温线
材料科学
计算机科学
作者
Jianxin Zhang,Junlin Ma,Wenrui Zhang,Hanwen Zhang,Xiaodong Geng,Kai Yang,Jiancheng Zhang,Hao-Yuan Mo,Wen Li,Bingzhang Lu,Xuhan Liu,Nan Zhu
标识
DOI:10.1021/acs.analchem.4c01511
摘要
The advent of wearable sensors heralds a transformation in the continuous, noninvasive analysis of biomarkers critical for disease diagnosis and fitness management. Yet, their advancement is hindered by the functional challenges affiliated with their active sensing analysis layer. Predominantly due to suboptimal intrinsic material properties and inconsistent dispersion leading to aggregation, thus compromising sensor repeatability and performance. Herein, an innovative approach to the functionalization of wearable electrochemical sensors was introduced, specifically addressing these limitations. The method involves a proton-induced self-assembly technique at the organic–water (O/W) interface, facilitating the generation of biomarker-responsive films. This research offers flexible, breathable sensor capable of real-time precision tracking l-cysteine (l-Cys) precision tracking. Utilizing an activation mechanism for Prussian blue nanoparticles by hydrogen peroxide, the catalytic core exhibits a specific response to l-Cys. The implications of this study refine the fabrication of film-based analysis electrodes for wearable sensing applications and the broader utilization of two-dimensional materials in functional-specific response films. Findings illuminate the feasibility of this novel strategy for precise biomarker tracking and extend to pave the way for constructing high-performance electrocatalytic analytical interfaces.
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