Non-enzymatic electrochemical sensing platform based on metal complex immobilized carbon nanotubes for glucose determination

被引:17
|
作者
Sonkar, Piyush Kumar [1 ]
Ganesan, Vellaichamy [1 ]
John, S. Abraham [2 ]
Yadav, Dharmendra Kumar [1 ]
Gupta, Rupali [1 ]
机构
[1] Banaras Hindu Univ, Inst Sci, Dept Chem, Varanasi 221005, Uttar Pradesh, India
[2] Gandhigram Rural Inst, Dept Chem, Gandhigram 624302, Tamil Nadu, India
来源
RSC ADVANCES | 2016年 / 6卷 / 108期
关键词
ELECTROCATALYTIC OXIDATION; MODIFIED ELECTRODE; HYDROGEN-PEROXIDE; NICKEL-HYDROXIDE; REDOX CATALYSIS; NANOPARTICLES; SENSOR; REDUCTION; ACID; NANOCOMPOSITE;
D O I
10.1039/c6ra16064f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This work demonstrates the preparation of an electrochemical sensing platform (ESP) based on nickel salophen (abbreviated as Ni-parallel to-S, where salophen is N,N'-bis(salicylidene)-1,2-phenylenediamine) immobilized multiwall carbon nanotubes (MWCNT) for electrochemical sensing of glucose in an alkaline medium. Ni-parallel to-S is immobilized onto MWCNT by stirring MWCNT and Ni-parallel to-S in DMF (MWCNT-Ni-parallel to-S). The MWCNT-Ni-parallel to-S is characterized by physicochemical and electrochemical techniques. Then, a glassy carbon (GC) electrode was modifies with the MWCNT-Ni-parallel to-S composite (GC/MWCNT-Ni-parallel to-S) and it exhibits efficient electrocatalytic activity towards glucose oxidation when compared to GC modified with Ni-parallel to-S. Cyclic voltammetry and chronoamperometry techniques are performed to understand the reaction kinetics and to determine the kinetic parameters such as electron transfer coefficient, rate constant of electrode reaction and catalytic rate constant. At the GC/MWCNT-Ni-parallel to-S ESP a linear calibration range for the glucose determination is observed from 500 nM to 20 mM with a limit of detection of 80 nM (S/N - 3) and sensitivity of 70 mu A mM(-1). Further, the present ESP is successfully utilized for the detection of glucose in a human blood serum sample with a good recovery (96.4-104.1%).
引用
收藏
页码:107094 / 107103
页数:10
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