Jeykumari D R Shobha, Narayanan S Sriman
Department of Analytical Chemistry, University of Madras, Chennai 600025, India.
Biosens Bioelectron. 2008 Jun 15;23(11):1686-93. doi: 10.1016/j.bios.2008.02.001. Epub 2008 Feb 13.
Mediated biosensors consisting of an oxidase and peroxidase (POx) have attracted increasing attention because of their wider applicability. This work presents a novel approach to fabricate nanobiocomposite bienzymatic biosensor based on functionalized multiwalled carbon nanotubes (MWNTs) with the aim of evaluating their ability as sensing elements in amperometric transducers. Electrochemical behavior of the bienzymatic nanobiocomposite biosensor is investigated by Faradaic impedance spectroscopy and cyclic voltammetry. The results indicate that glucose oxidase (GOD) and horseradish peroxidase (HRP) are strongly adsorbed on the surface of the thionin (TH) functionalized MWNTs and demonstrate a facile electron transfer between immobilized GOD/HRP and the electrode via the functionalized MWNTs in a Nafion film. The functionalized carbon nanotubes act as molecular wires to allow efficient electron transfer between the underlying electrode and the redox centres of enzymes through TH. Linear ranges for these electrodes are from 10nM to 10mM for glucose and 17nM to 56mM for hydrogen peroxide with the detection limit of 3 and 6nM, respectively. A remarkable feature of the bienzyme electrode is the possibility to determine glucose and hydrogen peroxide at a very low applied potential where the noise level and interferences from other electroactive compounds are minimal. Performance of the biosensor is evaluated with respect to response time, detection limit, selectivity, temperature and pH as well as operating and storage stability.
由氧化酶和过氧化物酶(POx)组成的介导型生物传感器因其更广泛的适用性而受到越来越多的关注。这项工作提出了一种基于功能化多壁碳纳米管(MWNTs)制备纳米生物复合双酶生物传感器的新方法,旨在评估其作为安培型传感器中传感元件的能力。通过法拉第阻抗谱和循环伏安法研究了双酶纳米生物复合生物传感器的电化学行为。结果表明,葡萄糖氧化酶(GOD)和辣根过氧化物酶(HRP)强烈吸附在硫堇(TH)功能化的MWNTs表面,并通过Nafion膜中的功能化MWNTs在固定化的GOD/HRP与电极之间实现了便捷的电子转移。功能化碳纳米管充当分子导线,通过TH使底层电极与酶的氧化还原中心之间实现高效电子转移。这些电极对葡萄糖的线性范围为10nM至10mM,对过氧化氢的线性范围为17nM至56mM,检测限分别为3nM和6nM。双酶电极的一个显著特点是能够在非常低的施加电位下测定葡萄糖和过氧化氢,此时噪声水平和来自其他电活性化合物的干扰最小。从响应时间、检测限、选择性、温度和pH以及操作和储存稳定性等方面评估了生物传感器的性能。