期刊文献+

基于金纳米棒/多壁碳纳米管-壳聚糖复合膜电极的肌红蛋白直接电化学和电催化研究

Direct Electrochemistry and Electrocatalysis of Myoglobin Based on AuNRs/ MWCNTs-Chit Composite Membrane Electrode
在线阅读 下载PDF
导出
摘要 采用金纳米棒(AuNRs)/多壁碳纳米管-壳聚糖(MWCNTs-Chit)复合膜促进肌红蛋白在电极上的直接电子转移,并用于构建H2O2生物传感器.首先将金纳米棒固定到玻碳电极表面,然后把MWCNTs-Chit分散溶液和肌红蛋白(Mb)固载到玻碳电极上,得到MWCNTs-Chit/Mb/AuNRs复合膜电极.通过循环伏安法对膜电极进行表征,在pH=7.0磷酸缓冲溶液中,Mb表现出一对峰形良好且可逆的氧化还原峰,其中氧化峰和还原峰电位分别为-0.291 V、-0.235 V,式电位(Eθ’)为-0.263 V.与此同时还探讨了修饰电极的电催化活性,结果表明其对H2O2具有良好的电催化还原作用,可作为检测H2O2的生物传感器.传感器对H2O2的米氏常数为0.0494 mM,线性范围为5.0×10-5~5.0×10-3M(R=0.986 7,n=10),检测限为3.2×10-6M(信噪比为3). A new H2O2 biosensor was fabricated based on the immobilization of myoglobin(Mb),gold nanorods(AuNRs),and multiwalled carbon nanotubes(MWCNTs)–chitosan(Chit) dispersed solution on glassy carbon electrode(GCE).The direct electron transfer of Mb on the MWCNTs-Chit/Mb/AuNRs modified glassy carbon electrode(GCE) was investigated.The immobilized Mb displayed a pair of well-defined and reversible redox peaks with the formal potential(Eθ') of-0.263V in 0.1M pH 7.0 PBS.The electrode reactions showed a surface-controlled process with a single proton transfer at the scan rate range from 10 to 500mV/s.Meanwhile,the reduction to H2O2 of biosensor was discussed.Its apparent Michaelis–Menten constant(KappM) for H2O2 was 0.049 4 mM,showing a good affinity.The experiment results showed that the linear range for H2O2 was from 5.0×10-5 to 5.0×10-3M,with a correlation coefficient of 0.986 7,and the detection limit of the sensor was 3.2×10-6M(S/N=3).Moreover,the biosensor showed a rapid response to H2O2,with a good stability and reproducibility.
出处 《湖北民族学院学报(自然科学版)》 CAS 2012年第1期6-10,14,共6页 Journal of Hubei Minzu University(Natural Science Edition)
基金 国家自然科学基金项目(20977074 21175115) 福建省教育厅科技项目(JA11168) 福建省研究生教育创新基地资金资助
关键词 肌红蛋白 多壁碳纳米管 壳聚糖 金纳米棒 H2O2生物传感器 memoglobin multi-walled carbon nanotubes chitosan gold nanorods(AuNRs) H2O2 biosensor
  • 相关文献

参考文献22

  • 1张旭志,焦奎.单壁碳纳米管和室温离子液体胶修饰电极[J].物理化学学报,2008,24(8):1439-1444. 被引量:9
  • 2Ozaki S,Matsui T,Roach M P,et al.Rational molecular design of a catalytic site:engineering of catalytic functions to the myoglobin active site frameworkCoordination Chemistry Reviews,2000.
  • 3Jia N Q,Wen Y L,Yang G F,et al.Direct electrochemistry and enzymatic activity of hemoglobin immobilized in ordered mesoporous titanium oxide matrixElectrochemistry Communications,2008.
  • 4Zou Y J,Xiang C L,Sun L X,et al.Amperometric glucose biosensor prepared with biocompatible material and carbon nanotube by layer-by-lay-er self-assembly techniqueElectrochimica Acta,2008.
  • 5Huang Y X,Zhang W J,Xian H,et al.An electrochemical investigation of glucose oxidase at a CdS nanoparticles modified electrodeBiosensors and Bioelectronics,2005.
  • 6Wang L Y,Kan X W,Zangh M C,et al.Fluorescence for the determination of protein with functionalized nano-ZnSThe Analyst,2002.
  • 7Ozoemena K I,Nkosi D,Pillay J.Influence of solution pH on the electron transport of the self-assembled nanoarrays of single-walled carbon nanotube-cobalt tetra-aminophthalocyanine on gold electrodes:Electrocatalytic detection of epinephrineElectrochimica Acta,2008.
  • 8Huang H W,He C C,Zeng Y L,et al.Preparation and optical properties of worm-like gold nanorodsJournal of Colloid and Interface Science,2008.
  • 9Chi Z H,Asher S A.UV Resonance Raman Determination of Protein Acid Denaturation:Selective Unfolding of Helical Segments of Horse Myoglo-binBiochemistry,1998.
  • 10Gan X,Liu T,Zhong J, et al.Effect of silver nanoparticles on the electron transfer reactivity and the catalytic activity of myoglobinChemBioChem,2004.

二级参考文献38

共引文献9

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