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一种基于水凝胶一步制备的用于监测大鼠脑微透析液中过氧化氢的耐用非酶电化学传感器。

A durable non-enzymatic electrochemical sensor for monitoring H2O2 in rat brain microdialysates based on one-step fabrication of hydrogels.

作者信息

Wang Zhen, Zhang Limin, Tian Yang

机构信息

Department of Chemistry, Tongji University, Siping Road 1239, Shanghai 200092, China.

出版信息

Analyst. 2015 Jun 7;140(11):3788-93. doi: 10.1039/c4an02003k.

Abstract

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.

摘要

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。

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