Wearable Sensor for Continuous Monitoring Multiple Biofluids: Improved Performances by Conductive Metal‐Organic Framework with Dual‐Redox Sites on Flexible Graphene Fiber Microelectrode

材料科学 微电极 石墨烯 可穿戴计算机 多电极阵列 对偶(语法数字) 氧化还原 纳米技术 导电体 纤维 光电子学 电极 计算机科学 复合材料 嵌入式系统 艺术 化学 文学类 物理化学 冶金
作者
Wei Huang,Yun Xu,Yong Yang,Jia Sun,Min Hu,F. Hao,Fei Xiao
出处
期刊:Advanced Functional Materials [Wiley]
标识
DOI:10.1002/adfm.202424018
摘要

Abstract Wearable sensors hold significant promise for continuous, real‐time, and non‐invasive analysis in biofluids. However, current wearable sensor technologies suffer from low accuracy for detecting trace analytes, inevitable signal distortion due to deformation, and inadequate biofluid replenishment. Herein, a wearable electrochemical sensor is developed by integrating designed metal‐organic frameworks (MOFs) modified graphene fiber (GF) microelectrode into a flexible microfluidic chip. The proposed atomically precise phthalocyanine‐based MOFs, with high‐density dual‐redox sites and intrinsic conductivity, ensure highly sensitive and selective electrochemical detection of the metabolite uric acid (UA) and tyrosine (Tyr) in biofluids. The freestanding, functionalized GF microelectrode is assembled from graphene nanosheets. Therefore, it exhibits excellent mechanical flexibility, a large surface area, and high temporal/spatial resolution. This contributes to a robust bio‐interface adaptable to various skin areas and improves the accuracy for in vivo detection. Consequently, the high‐performance electrochemical sensing system based on the GF microelectrode modified by dual‐redox‐sites MOFs, integrated with a microfluidic chip for efficient collection and rapid replenishment of raw biofluids, results in a practical wearable sensor for real‐time monitoring of UA and Tyr in sweat and saliva, which are utilized for non‐invasive gout management by tracking metabolite levels in gout patients and healthy controls during a purine‐rich dietary challenge.
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