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New Approach for Porous Chitosan–Graphene MatrixPreparation through Enhanced Amidation for Synergic Detection of Dopamineand Uric Acid

机译:多孔壳聚糖-石墨烯基体的新方法增强酰胺化制备多巴胺协同检测和尿酸

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摘要

Amide-functionalized materials have emerged as promising nonprecious catalysts for electrochemical sensing and catalysis. The covalent immobilization of chitosan (CS) onto graphene sheet (GS) (denoted as CS–GS) has been done via higher degree of amidation reaction to develop an electrochemical sensing matrix for simultaneous determination of dopamine (DA) and uric acid (UA). The enhanced amidation between CS and GS has not been reported previously. However, electrochemical results have revealed that the CS–GS enhances the electrocatalytic performance in terms of the oxidation potential and peak current due to the higher degree of amide functionalization compared to that of CS/GS, which has a lower amidation. Differential pulse voltammetry-based studies have indicated that the CS–GS matrix works at a lower detection limit (0.14 and 0.17 μM) (S/N = 3) and over a longer linear range (1–700 and 1–800 μM), with a comparatively higher sensitivity (2.5 and 2.0 μA μM–1 cm–2), for DA and UA, respectively. In addition, the CS–GS matrix demonstrates good selectivity toward the detectionof DA and UA in the presence of a 10-fold higher concentration ofAA and glucose. The as-prepared three-dimensional porous CS–GSalso endows selective determination toward DA and UA in various realsamples.
机译:酰胺官能化的材料已经成为有希望的用于电化学传感和催化的非贵金属催化剂。通过较高程度的酰胺化反应将壳聚糖(CS)共价固定在石墨烯片(GS)(表示为CS–GS)上,以开发用于同时测定多巴胺(DA)和尿酸(UA)的电化学传感基质。以前没有报道CS和GS之间的酰胺化增强。然而,电化学结果表明,与酰胺化程度较低的CS / GS相比,由于酰胺官能化程度较高,CS-GS在氧化电位和峰值电流方面增强了电催化性能。基于差分脉冲伏安法的研究表明,CS–GS基质在较低的检出限(0.14和0.17μM)(S / N = 3)和更长的线性范围(1–700和1–800μM)下工作,对DA和UA的灵敏度分别较高(分别为2.5和2.0μAμM –1 cm –2 )。此外,CS-GS基质对检测具有良好的选择性浓度高10倍的DA和UA时AA和葡萄糖。准备好的三维多孔CS–GS还赋予了DA和UA各种实际选择权样品。

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