微分脉冲伏安法
介电谱
循环伏安法
电化学气体传感器
化学
电极
傅里叶变换红外光谱
分析化学(期刊)
热重分析
电化学
检出限
无机化学
差示扫描量热法
材料科学
伏安法
Zeta电位
电解质
电催化剂
热解炭
生物传感器
核化学
化学工程
催化作用
红外光谱学
血清
作者
Hafsa Shafique,Iram Naz,Muhammad Bilal Khan Niazi,Akhtar Hayat,Farhat Jubeen
出处
期刊:Langmuir
[American Chemical Society]
日期:2026-04-27
卷期号:42 (18): 13141-13153
标识
DOI:10.1021/acs.langmuir.6c01509
摘要
Being biological markers of several cardiovascular and neurological diseases, the detection and maintenance of dopamine (DA) and uric acid (UA) concentrations in blood are significant. However, the development of an electrochemical sensor that provides strongly resolved signals for the simultaneous evaluation of a broad range of DA and UA is still a challenge. A pencil graphite electrode (PGE)-based electrochemical sensor was developed by integrating the electrocatalytic properties of zeolitic imidazolate framework (ZIF-67) with a benzidine-melamine-terephthalaldehyde covalent organic framework (Bz-Mm-Tp-COF) for the simultaneous detection of DA and UA via differential pulse voltammetry (DPV). ZIF-67 permitted strong catalytic activity due to the incorporation of cobalt, whereas the COF offered an extensive electrochemical surface area along with stabilizing the composite through π-π interaction. Taking advantage of both, the ZIF-67/Bz-Mm-Tp-COF composite exhibited a large specific surface area, efficient catalytic activity, and nitrogen-rich groups, leading to hydrogen bonding with analyte molecules. The structural morphology of the composite was substantiated by field emission electron microscopy (FESEM), Fourier transform infrared spectroscopy (FTIR), powder X-ray diffraction (PXRD), thermogravimetric analysis-differential scanning calorimetry (TGA-DSC), and zeta potential. Whereas, fabricated electrodes were electrochemically characterized via cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and differential pulse voltammetry (DPV). The ZIF-67/Bz-Mm-Tp-COF@PGE sensor demonstrated a wide linear dynamic range of 0.001-250 μM and 0.001-1200 μM for DA and UA, respectively, spanning both physiological and pathological concentration windows relevant to clinical monitoring. The limits of detection (LOD) were determined to be 0.3 and 0.6 nM for DA and UA, respectively, calculated at a signal-to-noise ratio of 3. This may be attributed to the high electroactive surface area and efficient charge transfer facilitated by the composite architecture. An anti-interference study assured the selectivity of the designed electrochemical sensor. Following the practical applicability, an outstanding recovery percentage (95.8-108.3%) was obtained for spiked blood samples.
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