材料科学
葡萄糖氧化酶
生物传感器
纳米技术
电极
可穿戴计算机
制作
生物医学工程
铂金
选择性
固定化酶
微电极
线性
膜
安培法
白金黑
可穿戴技术
表面改性
连续血糖监测
响应时间
灵敏度(控制系统)
电流密度
催化作用
作者
Hyeong Jun Kim,Byeong Jun So,Yuseung Choi,Eunhyung Nam,Gilyong Shin,Ju Hwan Lee,Tae June Kang
标识
DOI:10.1021/acsami.5c19085
摘要
Microneedle-based glucose sensors offer a minimally invasive and wearable platform for real-time monitoring. However, conventional enzyme immobilization methods often lack spatial precision and show limited compatibility with miniaturized electrode architectures. Here, we present an electrodeposition strategy for localized and controlled immobilization of glucose oxidase at microneedle tips. Dendritic platinum was engineered via potentiostatic diffusion-limited growth, significantly increasing electroactive surface area and enzyme loading capacity. This yielded an enhanced catalytic response with a maximum current density of ∼200 μA/cm 2 during glucose oxidation, thereby improving sensitivity. To ensure selectivity, o -phenylenediamine electropolymerization time was optimized to balance glucose permeability with suppression of electroactive interferents, reducing interferent-to-glucose current ratios to below 4.0% in artificial interstitial fluid. In human trials, the microneedle sensor operated stably and exhibited a sensitivity of 137.7 nA·(mg/dL) −1 (≈2.48 μA·mM –1 ), with strong linearity ( R 2 = 0.940) across 82–211 mg/dL (≈4.6–11.7 mM). This scalable and tunable fabrication approach addresses the dual challenge of achieving high sensitivity and selectivity in miniaturized enzymatic sensors, offering broad potential for wearable biosensing and personalized healthcare technologies.
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