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电化学还原氧化石墨烯/纳米金-壳聚糖复合膜修饰玻碳电极对尿酸的灵敏测定

吴玲 曹忠 宋天铭 宋铖 谢晶磊 何婧琳 肖忠良

分析化学Issue(11):1656-1660,5.
分析化学Issue(11):1656-1660,5.DOI:10.11895/j.issn.0253-3820.140357

电化学还原氧化石墨烯/纳米金-壳聚糖复合膜修饰玻碳电极对尿酸的灵敏测定

A Glassy Carbon Electrode Modified with Electrochemically Reduced Graphene Oxide/Gold Nanoparticles-Chitosan Composite Film for Sensitive Determination of Uric Acid

吴玲 1曹忠 1宋天铭 1宋铖 1谢晶磊 1何婧琳 1肖忠良1

作者信息

  • 1. 长沙理工大学,化学与生物工程学院,电力与交通材料保护湖南省重点实验室,长沙410004
  • 折叠

摘要

Abstract

Anelectrochemicallyreducedgrapheneoxide/goldnanoparticle-chitosan(ERGO/AuNP-CS) composite film modified glassy carbon electrode ( GCE) was constructed by directly electrochemical reduction of GO, and then assembly of AuNP-CS polycation on the surface. The surface morphologies of different modified electrodes including bare GCE, GCE/GO, GCE/ERGO and GCE/ERGO/AuNP-CS were characterized by scanning electron microscopy ( SEM ) . The differential pulse voltammetric behaviors of the electrodes were investigated, and the results indicated that the composite of ERGO/AuNP-CS exhibited excellent electrocatalytic oxidation activity to uric acid ( UA) molecule. In 0. 10 mol/L of phosphate buffer solution (pH=6. 5) with a scanning rate of 100 mV/s, the proposed composite film modified electrode showed a linear electrochemical response to UA in the range of 0 . 05-110 μmol/L with a detection limit of 12. 4 nmol/L ( S/N = 3 ). The electrode displayed good selectivity, reproducibility and stability in the determination of UA in human serum and urine samples with a recovery of 93 . 8%-104 . 1%. The detection results were agreed with those of conventional spectrophotometry and uricase Kit methods.

关键词

电化学还原氧化石墨烯/纳米金-壳聚糖聚阳离子/尿酸/电催化氧化/修饰电极

Key words

Electrochemicallyreducedgrapheneoxide/Goldnanoparticle-chitosanpolycation/Uricacid/Electrocatalytic oxidation/Modified electrode

引用本文复制引用

吴玲,曹忠,宋天铭,宋铖,谢晶磊,何婧琳,肖忠良..电化学还原氧化石墨烯/纳米金-壳聚糖复合膜修饰玻碳电极对尿酸的灵敏测定[J].分析化学,2014,(11):1656-1660,5.

基金项目

国家科技支撑计划(Nos.2012BAD31B08,2012BAC17B01)、国家自然科学基金(Nos.21275022,21105005)、湖南省科技计划(No.2013FJ3075)项目资助This work was supported by the National High Technology Research and Development Program of China ( No.2012BAD31B08,2012BAC17B01) and the National Natural Science Foundation of China (Nos.21275022,21105005) (Nos.2012BAD31B08,2012BAC17B01)

分析化学

OA北大核心CSCDCSTPCDSCI

0253-3820

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