### 分子印迹电化学传感器选择性识别及电催化检测多巴胺

1. 桂林理工大学化学与生物工程学院 桂林 541004
• 投稿日期:2012-12-28 发布日期:2013-03-26
• 通讯作者: 李建平,likianping@263.net E-mail:likianping@263.net
• 基金资助:

项目受国家自然科学基金(No. 21165007)和广西自然科学基金(No. 2012GXNSFAA053032)资助.

### A Molecular Imprinted Electrochemical Sensor For Selectively and Electro-catalytically Voltammetric Determination of Dopamine

Wei Xiaoping, Chang Chuan, Li Jianping

1. College of Chemistry and Bioengineering, Guilin University of Technology, Guilin 541004
• Received:2012-12-28 Published:2013-03-26
• Supported by:

Project supported by the Natural Science Foundation of China (No. 21165007) and Guangxi Natural Science Foundation (No. 2012GXNSFAA053032).

A novel strategy for improving the sensitivity of molecular imprinted electrochemical sensor was proposed and dopamine (DA) was selected as the template molecular in this assay. The electroactive membrane of poly-bromophenol blue (BB) which was polymerized on the electrode surface acted as molecular imprinted membrane of DA. To prepare poly-BB-DA molecularly imprinted polymer (MIP), CV scans were performed for 30 cycles in the potential range between -1.0 and 1.8 V at 50 mV/s in an acetate buffer solution (pH=4.0) containing 1.0×10-3 mol/L DA and 3.0×10-3 mol/L BB at 25 ℃. The MIP electrode was washed by methanol (50% in volume) for 12 min to remove template molecules. Differential pulse voltammetry (DPV) was performed after the rebinding reaction of the DA and the MIP membrane in DA sample solutions for 6 min. With the increasing of the DA concentration, the binding sites in the membrane taken by DA molecules also increased, so was the peak current in the DPV analysis. The sensitivity was improved significantly due to the signal amplifying effect produced by the catalytic effect of electro oxidation of dopamine on BB membrane. The experimental conditions were also optimized. Electrochemical measurements for the MIP membrane characterization were carried out in the supporting electrolyte of 0.01 mol/L K3[Fe(CN)6] solution containing 0.5 mol/L KCl. CV was performed from -0.2 to 0.6 V at a scan rate of 100 mV/s. DPV was performed in the supporting electrolyte of 0.1 mol/L PBS (pH 7.4) over a potential range of -0.1 to 0.6 V, with the pulse amplitude of 50 mV and the scan rate of 50 mV/s. All measurements were carried out at room temperature (25 ℃). DA was determined by DPV, and there was a linear relationship between oxidation currents and DA concentrations in the range of 0～1.2×10-6 mol/L with a detection limit of 1.62×10-10 mol/L. This is one of the most sensitive sensors for DA determination due to the catalytic oxidation of DA on electroactive MIP.