期刊
SENSORS
卷 22, 期 7, 页码 -出版社
MDPI
DOI: 10.3390/s22072787
关键词
microneedle electrode array; continuous glucose monitoring; wireless data transmission; chronoamperometry; platinum black; glucose sensor
资金
- Korea Environment Industry & Technology Institute (KEITI) through the Technology Development Project for Biological Hazards Management in Indoor Air Project - Korea Ministry of Environment (MOE) [G232021010381]
- National Research Foundation of Korea [NRF-2020M3A9E4104385]
- National Research Foundation of Korea [2020M3A9E4104385] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
Miniaturization and wireless continuous glucose monitoring play vital roles in diabetes management. The authors have developed a microneedle-based enzyme-free electrochemical wireless sensor for painless and continuous glucose monitoring.
Miniaturization and wireless continuous glucose monitoring are key factors for the successful management of diabetes. Electrochemical sensors are very versatile and can be easily miniaturized for wireless glucose monitoring. The authors report a microneedle-based enzyme-free electrochemical wireless sensor for painless and continuous glucose monitoring. The microneedles (MNs) fabricated consist of a 3 x 5 sharp and stainless-steel electrode array configuration. Each MN in the 3 x 5 array has 575 mu m x 150 mu m in height and width, respectively. A glucose-catalyzing layer, porous platinum black, was electrochemically deposited on the tips of the MNs by applying a fixed cathodic current of 2.5 mA cm(-2) for a period of 200 s. For the non-interference glucose sensing, the platinum (Pt)-black-coated MN was carefully packaged into a biocompatible ionomer, nafion. The surface morphologies of the bare and modified MNs were studied using field-emission scanning electron microscopy (FESEM) and energy-dispersive X-ray analysis (EDX). The wireless glucose sensor displayed a broad linear range of glucose (1 -> 30 mM), a good sensitivity and higher detection limit of 145.33 mu A mM(-1) cm(-2) and 480 mu M, respectively, with bare AuMN as a counter electrode. However, the wireless device showed an improved sensitivity and enhanced detection limit of 445.75, 165.83 mu A mM(-1) cm(-2) and 268 mu M, respectively, with the Pt-black-modified MN as a counter electrode. The sensor also exhibited a very good response time (2 s) and a limited interference effect on the detection of glucose in the presence of other electroactive oxidizing species, indicating a very fast and interference-free chronoamperometric response.
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