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首页> 外文期刊>Journal of Electroanalytical Chemistry: An International Journal Devoted to All Aspects of Electrode Kinetics, Interfacial Structure, Properties of Electrolytes, Colloid and Biological Electrochemistry >Electrochemical detection of uric acid using graphite screen-printed electrodes modified with Prussian blue/poly(4-aminosalicylic acid)/Uricase
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Electrochemical detection of uric acid using graphite screen-printed electrodes modified with Prussian blue/poly(4-aminosalicylic acid)/Uricase

机译:使用普鲁士蓝/聚(4-氨基水杨酸)/尿液酶改性石墨丝网印刷电极的尿酸电化学检测

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AbstractThis work investigates the use of electrochemical platforms containing polymeric films derived from 4-aminosalicylic acid (4-ASA) modified with the enzyme urate oxidase (UOx) for quantification of uric acid (UA) in urine samples. Electropolymerization of 4-ASA was investigated over carbon graphite electrodes (CGE). As a mediator of the enzymatic product, Prussian blue (PB) was also electrodeposited over the working electrodes. The film provides electrochemical activity with a homogeneous coverage, and the use of PB does not alter the electrochemical profile or the film morphology. Analysis of infrared spectra demonstrates the presence of the unchanged carboxyl groups and suggests that polymerization begins at the nitrogen atom. The biosensor was developed on graphite screen-printed electrodes with all optimization performed on CGE. UOx was immobilized through physical adsorption and the proposed sensor was coupled to a flow cell in a flow injection analysis (FIA) system with amperometric detection. The flow rate, injection volume, and pH of the UA solution were optimized at 2.10mLmin?1, 200μL, and 8.27, respectively. Under these conditions, a relative standard deviation of 2.15% (n=10) was achieved for UA detection. A linear range of 10 to 200μM was obtained for UA determination with a limit of detection of 3.0μM. UA recovery from amended urine samples was 97.4% (±2.4).Graphical abstract
机译:<![cdata [ 抽象 本作研究调查了含有衍生自4-氨基水杨酸(4-ASA)的聚合物膜的电化学平台的使用用酶尿酸盐氧化酶(UOX)用于定量尿液样品中的尿酸(UA)。在碳石墨电极(CGE)上研究了4-ASA的电聚合。作为酶促产品的介体,普鲁士蓝(PB)也在工作电极上电沉积。薄膜提供具有均匀覆盖的电化学活性,并且Pb的使用不会改变电化学曲线或薄膜形态。红外光谱分析证明存在不变的羧基并表明聚合在氮原子处开始。在石墨丝网印刷电极上开发了生物传感器,在CGE上进行了所有优化。通过物理吸附使UOX固定,并且所提出的传感器与流动注射分析(FIA)系统中的流动细胞偶联,具有电流检测。流速,注射体积和UA溶液的pH值在2.10mLmin优化 1 ,200μL,和8.27,分别。在这些条件下,对UA检测实现了2.15%(n = 10)的相对标准偏差。获得10至200μm的线性范围,用于UA测定,其检测限为3.0μm。从修正的尿液样本中恢复为97.4%(±2.4)。 图形摘要

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