化学
检出限
抗坏血酸
金属有机骨架
电极
玻璃碳
氧化还原
导电体
无机化学
纳米技术
电化学
循环伏安法
分析化学(期刊)
色谱法
有机化学
吸附
物理化学
材料科学
复合材料
食品科学
作者
Michael L. Ko,Lukasz Mendecki,Aileen M. Eagleton,Claudia G. Durbin,Robert M. Stolz,Zheng Meng,Katherine A. Mirica
摘要
This paper describes the first implementation of an array of two-dimensional (2D) layered conductive metal–organic frameworks (MOFs) as drop-casted film electrodes that facilitate voltammetric detection of redox active neurochemicals in a multianalyte solution. The device configuration comprises a glassy carbon electrode modified with a film of conductive MOF (M3HXTP2; M = Ni, Cu; and X = NH, 2,3,6,7,10,11-hexaiminotriphenylene (HITP) or O, 2,3,6,7,10,11-hexahydroxytriphenylene (HHTP)). The utility of 2D MOFs in voltammetric sensing is measured by the detection of ascorbic acid (AA), dopamine (DA), uric acid (UA), and serotonin (5-HT) in 0.1 M PBS (pH = 7.4). In particular, Ni3HHTP2 MOFs demonstrated nanomolar detection limits of 63 ± 11 nM for DA and 40 ± 17 nM for 5-HT through a wide concentration range (40 nM–200 μM). The applicability in biologically relevant detection was further demonstrated in simulated urine using Ni3HHTP2 MOFs for the detection of 5-HT with a nanomolar detection limit of 63 ± 11 nM for 5-HT through a wide concentration range (63 nM–200 μM) in the presence of a constant background of DA. The implementation of conductive MOFs in voltammetric detection holds promise for further development of highly modular, sensitive, selective, and stable electroanalytical devices.
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