Direct Electrochemistry of Hemoglobin Immobilized in the Sodium Alginate and SiO2 Nanoparticles Bionanocomposite Film on a Carbon Ionic Liquid Electrode

被引:17
|
作者
Sun, W. [1 ]
Wang, D. [1 ]
Zhai, Z. [1 ]
Gao, R. [1 ]
Jiao, K. [1 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Minist Educ, Key Lab Ecochem Engn, Qingdao 266042, Shandong, Peoples R China
基金
中国国家自然科学基金; 芬兰科学院;
关键词
1-Butyl-3-methylimidazolium hexafluorophosphate; Hemoglobin; Direct electron transfer; Carbon paste electrode; SiO2; nanoparticle; LAYER-BY-LAYER; HEME-PROTEINS; GLUCOSE-OXIDASE; ASCORBIC-ACID; NITRIC-OXIDE; URIC-ACID; ELECTROCATALYSIS; PASTE; ADSORPTION; BIOELECTROCHEMISTRY;
D O I
10.1007/BF03245852
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this paper a carbon ionic liquid electrode (CILE) was fabricated by using a room temperature ionic liquid of 1-butyl-3-methylimidazolium hexafluorophosphate (BMIMPF6) as binder. By using the CILE as basal electrode, the hemoglobin (Hb) molecule was immobilized on the surface of CILE with a sodium alginate (SA) hydrogel and SiO2 nanoparticles organic-inorganic composite material. The direct electrochemical behaviors of Hb in the bionanocomposite film were further studied in a pH 7.0 Britton-Robinson (B-R) buffer solution. A pair of well-defined quasi-reversible cyclic voltammetric peaks of Hb was obtained on SA/nano-SiO2/Hb/CILE with the formal potential (E-0') at -0.355 V (vs. SCE), which was the characteristic of heme Fe(III)/Fe(II) redox couples. The formal potential of Hb Fe(III)/Fe(II) couple shifted negatively with increasing pH of solution with a slope of -45.2 mV/pH, which indicated that a one electron transfer accompanied with one proton transportation. The immobilized Hb showed good electrocatalytic manner to the reduction of trichloroacetic acid (TCA).
引用
收藏
页码:412 / 419
页数:8
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