Ammam Malika, Fransaer Jan
Department of Metallurgy and Materials Engineering (MTM), KU Leuven, Kasteelpark Arenberg 44, B-3001 Heverlee, Belgium.
Biosens Bioelectron. 2009 Sep 15;25(1):191-7. doi: 10.1016/j.bios.2009.06.036. Epub 2009 Jul 1.
The electrophoretic deposition of glucose oxidase from water using asymmetrical alternating voltages is investigated. Using asymmetric voltages, glucose oxidase layers with a thickness of 7 microm could be deposited on a platinum electrode in 20 min time as verified with a microbalance, carbon analysis and scanning electron microscopy. In contrast, if a symmetrical alternating signal is used under the same conditions, a layer of 0.5 microm is formed. We believe the deposition is due to two effects: the electrophoretic migration of the enzyme towards the deposition electrode and the pH induced precipitation of the enzyme near the deposition electrode. The electrophoretic migration is due to the non-linear dependence of the electrophoretic mobility on the electric field caused by the asymmetry of the applied alternating current signal. In addition, pH changes near the deposition electrode drive the enzyme towards its point of zero charge (PZC), perhaps causing the precipitation of GOx on the substrate. The effect of amplitude, frequency, deposition time and GOx concentration on the deposition rate was studied. An amplitude of 160 V(p-p) and a frequency of 30 Hz was found to be optimal for the formation of thick enzyme layers, which excludes a big part of the interferences.
研究了使用不对称交变电压从水中电泳沉积葡萄糖氧化酶的过程。通过微天平、碳分析和扫描电子显微镜验证,使用不对称电压时,在20分钟内可在铂电极上沉积厚度为7微米的葡萄糖氧化酶层。相比之下,在相同条件下使用对称交变信号时,会形成0.5微米厚的层。我们认为这种沉积归因于两种效应:酶向沉积电极的电泳迁移以及pH诱导酶在沉积电极附近沉淀。电泳迁移是由于所施加交变电流信号的不对称性导致电泳迁移率对电场的非线性依赖性。此外,沉积电极附近的pH变化将酶驱向其零电荷点(PZC),这可能导致葡萄糖氧化酶在底物上沉淀。研究了振幅、频率、沉积时间和葡萄糖氧化酶浓度对沉积速率的影响。发现160V(峰-峰)的振幅和30Hz的频率对于形成厚酶层是最佳的,这排除了大部分干扰。