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Graphene Oxide-Based Nanomaterials for the Electrochemical Sensing of Isoniazid

纳米材料 石墨烯 氧化物 异烟肼 电化学 纳米技术 材料科学 检出限 化学 医学 冶金 电极 物理化学 病理 肺结核 色谱法
作者
Lanting Qian,Antony R. Thiruppathi,Joshua van der Zalm,Aicheng Chen
出处
期刊:ACS applied nano materials [American Chemical Society]
卷期号:4 (4): 3696-3706 被引量:84
标识
DOI:10.1021/acsanm.1c00178
摘要

Isoniazid is one of the most important antibiotics used for the treatment of tuberculosis. However, the associated side effects can be quite detrimental to human health, thus necessitating careful monitoring of the drug concentration in the human system. Here, we endeavored to understand the significant roles of oxygen and the structure of graphene oxide (GO) in developing high-performance graphene-based electrochemical sensors for the detection of isoniazid. Several graphene-based materials, including GO, thermally reduced graphene oxide (TrGO), electrochemically reduced graphene oxide (erGO), and interconnected reduced graphene oxide (IC-rGO) were synthesized to test their performance in the sensing of isoniazid. We found that a lower oxygen content on graphene sheets significantly promoted the electrochemical oxidation of isoniazid. Through the use of density functional theory (DFT) calculations, it was concluded that the oxygen functional groups on the graphene oxide sensors and the carboxamide functional groups of isoniazid exhibited repulsive forces that prevented isoniazid from approaching the graphene sheet, which consequently lowered the adsorption energy. To examine the structure of GO-based materials for the sensing of isoniazid, we successfully synthesized three-dimensional (3D) IC-rGO, with the intention of maximizing the electrochemically active surface area (ECSA) to increase the current response of the sensor for the electrochemical detection of isoniazid. An improved performance was observed for IC-rGO in contrast to the other GO-based nanomaterials; the optimized IC-rGO sensor had a detection limit of 0.03 μM with a high sensitivity of 4.02 μA μM–1 cm–2. Furthermore, the sensor exhibited a reproducible and stable response and negligible interference from the common biological species found in the blood and urine. The developed sensor was observed to successfully detect isoniazid in urine and blood serum, which confirmed its promising applicability in medical and biomedical applications.
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