Wang Zhen, Zhang Limin, Tian Yang
Department of Chemistry, Tongji University, Siping Road 1239, Shanghai 200092, China.
Analyst. 2015 Jun 7;140(11):3788-93. doi: 10.1039/c4an02003k.
A non-enzymatic electrochemical H2O2 sensor was developed by in situ fabrication of biocompatible chitosan (CS) hydrogels, in which a specific recognition molecule for H2O2, thionine (TH), was stably immobilized via one-step electrodeposition. Electron transfer of TH was facilitated in the CS/GPTMS/TH (GPTMS: γ-glycidoxypropyltrimethoxysiloxane) hydrogels with an electron transfer rate constant (ks) of 3.5 ± 0.1 s(-1). Meanwhile, TH in CS hydrogels maintained high electrocatalytic activity toward H2O2. The developed sensor exhibited a fast amperometric response toward H2O2 within 7 s and a linear response for H2O2 ranging from 5.0 × 10(-6) to 6.9 × 10(-4) M with a detection limit of 1.0 × 10(-6) M. In addition, the non-enzymatic electrochemical sensor exhibited long-term stability with a current decrease less than 5.0% in 18 days and good reproducibility with a small deviation of 7.2%. The remarkable analytical performance of the present sensor provided a promising model for durable monitoring of H2O2 in rat brain microdialysates, which is very useful for understanding the biological effects of H2O2 on the pathological and physiological processes.
通过原位制备生物相容性壳聚糖(CS)水凝胶,开发了一种非酶电化学H2O2传感器,其中通过一步电沉积稳定固定了H2O2的特异性识别分子硫堇(TH)。在电子转移速率常数(ks)为3.5±0.1 s(-1)的CS/GPTMS/TH(GPTMS:γ-缩水甘油氧基丙基三甲氧基硅氧烷)水凝胶中,TH的电子转移得到促进。同时,CS水凝胶中的TH对H2O2保持高电催化活性。所开发的传感器对H2O2在7秒内表现出快速的安培响应,对H2O2的线性响应范围为5.0×10(-6)至6.9×10(-4) M,检测限为1.0×10(-6) M。此外,该非酶电化学传感器表现出长期稳定性,在18天内电流下降小于5.0%,并且具有良好的重现性,偏差小至7.2%。本传感器卓越的分析性能为大鼠脑微透析液中H2O2的持久监测提供了一个有前景的模型,这对于理解H2O2对病理和生理过程的生物学效应非常有用。