期刊文献+

基于纳米MnO2二茂铁修饰丝网印刷碳电极的尿酸生物传感器研究 被引量:3

A Uric Acid Biosensor Based on Screen Printed Carbon Electrode Modified by MnO_2 Nano-Particles and Ferrocene
下载PDF
导出
摘要 在丝网印刷碳电极上修饰纳米MnO2,并利用戊二醛和β-环糊精交联固定尿酸酶,以二茂铁作为电子媒介体,研制用于测定尿酸浓度的生物传感器。实验结果表明,纳米MnO2降低了电子媒介体二茂铁的氧化还原反应电位,且纳米MnO2与电子媒介体二茂铁在尿酸生物传感器中表现出协同增效效应。该尿酸生物传感器线性响应范围是6.0×10^-6~1.2×10^-3mol/L,检出限为3.0×10^-6mol/L。用纳米MnO2修饰酶电极.改善了电极表面条件,加快了电极反应速率,提高了尿酸传感器的灵敏度。 A novel biosensor is developed to determine the uric acid. It is prepared by utilizing glutaraldehyde cross linked β-cyelodextrin to immobilize the uricase on the surface of screen printed carbon paste electrodes which was modified by MnO2 nano-particles, and ferrocene is employed as an electron transfer mediator. The results show that MnO2 nano-particles reduce the redox potential of ferrocene, furthermore Mn()2 nano-particles and ferrocene improve the current response of the uric acid biosensor as a synergetic effect. The uric acid biosensor's linear range is 6.0×10^-6 to 1.2 ×10^-3 mol/L with a detection limit of 3. 0 ×10^-6 mol/L. Compared with the electrode modified by ferrocene, the electrode modified with both ferrocene and MnO2 nano-particles sped up the electrode reaction and improves the sensitivities of the sensor by two-fold.
出处 《分析科学学报》 CAS CSCD 北大核心 2009年第1期79-82,共4页 Journal of Analytical Science
基金 宁波工程学院科技项目(2005028)
关键词 纳米MNO2 尿酸酶 二茂铁 Β-环糊精 丝网印刷碳电极 生物传感器 MnO2 nano-particle Uricase Ferrocene β-cyclodextrin Screen-printed carbon electrodes Biosensor
  • 相关文献

参考文献9

二级参考文献49

  • 1万平玉,潘军青,孙艳芝,刘小光.NaBiO_3的固相合成及其对二氧化锰电化学性质的影响[J].电源技术,2005,29(1):38-40. 被引量:14
  • 2Wang J,Electroanalysis,1989年,1卷,1期,43页
  • 3Matsubara C, Kawamoto N, Takamura K. Oxo [5, 10, 15,20 - tetra(4 - pyridyl)poyphyrinato] titanium (IV) - An ultra - high sensitivity spectrophotometric reagent for hydrogen peroxide[J]. Analyst, 1992, 117:1781 - 1 784.
  • 4Nakashima K, Maki K, Kawaguchi S, et al. Peroxyoxalate chemiluminescence assay of hydrogen peroxide and glucose using 2, 4, 6, 8-Tetrathio- morpholinopyrimido[5, 4 - d] pyrimidine as a fluorescent component[J]. Anal. Sci., 1991, 7:709-714.
  • 5Oungpipat W, Alexander P W, Southwell - Keely P. A reagentless amperometric Biosensor for hydrogen peroxide determination based on asparagus tissue and ferrocene mediation[J]. Anal. Chim. Acta, 1995, 309:35 -45.
  • 6Fortier G, Vaillancourt M, Belanger D. Evalution of nafion as media for glucose oxidase immobilization for the development of an amperometric glucose biosensor[J].Electroanalysis, 1992, 4:275 - 283.
  • 7Sun C Q, Li W J, Sun Y P, et al. Fabrication of multilayer films containing horseradish peroxide sensor[J]. Electrochimica Acta, 1999, dd: 3 d01 - 3 407.
  • 8Goudaa M D, Kumarb M A, Thakura M S, et al. Enhancement of operational stability of an enzyme biosensor for glucose and sucrose using protein based stabilizing agents[J]. Biosensors and Bioelectronic, 2002, 17:503 - 507.
  • 9Garjonyte R, Malinauskas A. Electrocatalytic reactions of hydrogen peroxide at carbon paste electrodes modified by some metal hexacyanoferrates[J]. Sensors and Actuators B. 1998, 46:236-241.
  • 10Guilbgault G G. Analytical Uses of Immobilized Enzymes, Marcel Dekker, New York, 1984

共引文献38

同被引文献31

引证文献3

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部