期刊
SENSORS AND ACTUATORS B-CHEMICAL
卷 243, 期 -, 页码 203-210出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.snb.2016.11.145
关键词
Ir NPs; TMB; H2O2; Xanthine; Benzoyl peroxide; Artemisinin
资金
- National Natural Science Foundation of China [21175060, 21403090]
- Fundamental Research Funds for the Central Universities [JUSRP51507]
- 111 Project [B13025]
A facile and efficient method was developed for the preparation of iridium nanoparticles NPs) with superior peroxidase-like activity. Under the catalytic action of the Ir NPs, the peroxidase substrate 3,3,5,5tetramathylbenzidine (TMB) can be oxidized by H2O2 to form a blue -colored production oxTMB. Kinetic analysis indicated that the catalytic behavior was in accordance with the typical Michaelis-Menten kinetics and the catalytic reaction followed the ping -pang mechanism. Electron Spin Resonance (ESR) experiment showed that no hydroxyl radical formed in the reaction process. Peroxide substrates with different electron withdrawing ability (benzoyl peroxide, H2O2 and artemisinin) were used to study the catalytic reactions and results indicated that H2O2 can oxidize TMB with much faster rate than artemisinin and slower rate than benzoyl peroxide. These results suggest an electron transfer mechanism was involved in the system of TMB-H2O2-Ir NPs. By using TMB as the colorimetric substrate, H2O2 can be rapidly determined and the method was extended for the determination of xanthine based on its production of H2O2 in the presence of xanthine oxidase. The prepared 1r NPs exhibit good stability in wide range of pH and temperature. The Ir NPs retained at least 90% of their initial catalytic activity after stored at ambient temperature for three months. The high specificity for H2O2 and the excellent stability of the peroxidase-like Ir NPs showed the great application potential in biotechnology field. (C) 2016 Elsevier B.V. All rights reserved.
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