Dopamine (DA) is a very important neurotransmitter in the mammalian central nervous system. Because low levels of DA have been found in patients with Parkinson's disease, 1 its detection with high selectivity and sensitivity is of great significance in investigating its physiological functions and the diagnose of nervous diseases resulting from an abnormal metabolite. When solid electrodes are used to detect DA, the main and foremost difficulty is the interference of ascorbic acid (AA), which is oxidized at almost the same potential as DA.2 It is thus very important to develop an electrochemical method of high selectivity and sensitivity for the determination of DA.Chitosan, which is derived from chitin, has excellent biologic compatibility and can be used as a modifier because it has many amino and hydroxyl groups.3-8 Besides, using a natural polymer as a dispersant is a requirement of environment protection. Carbon nanotubes have attracted much attention because they have the ability to promote electron transfer reactions when used as electrode materials, 9,10 but carbon nanotubes are very stable and insoluble in most solvents, which restrained its application in electroanalysis. Thus, in this study, a multiwall carbon nanotube (MWNT)-chitosan modifier was obtained by putting MWNT into a chitosan solution (0.5%). The MWNTchitosan modified electrode (MC/GCE) has many advantages with regard to a low detection limit, a fast response, excellent reproducibility for the detection for DA and AA simultaneously.
Experimental
ApparatusAll of the electrochemical measurements were carried out with a bioanalytical system CV-50W electrochemical analyzer. The three-electrode system consisted of a modified GCE, a saturated calomel reference electrode (SCE), and a platinum auxiliary electrode. All potentials were referred to the SCE. The transmission electron microscopy image was done with a TEM-100CXII.
ReagentsDopamine, ascorbic acid (Fluka Corp.). A chitosan solution (0.5%) was prepared by dissolving 0.05 g of chitosan in 10 ml acetic acid (2 mol l -1 ). 11 The MWNT used in this work (obtained from the Institute of Nanometer, Central China Normal University) was synthesized by catalytic pyrolysis and purified followed the method given in a reference.
12
Preparation for a MWNT-chitosan modified electrodeUpon putting 1 mg of MWNT into 5 mL of a chitosan solution (0.5%), ultrasonic agitation for a few minutes gave 0.2 mg ml -1 of a black suspension. Before being modified, the GCE was polished with 0.3 µm and 0.05 µm aluminum slurry, rinsed thoroughly with redistilled water, then ultrasonically rinsed with alcohol, redistilled water for 1 min each, and dried under an infrared lamp. After the GCE was cooled, it was smeared evenly with 10 µl of a MWNT-chitosan (0.5%) solution by a micro-syringe, and then dried under an infrared lamp for 10 min. After cooling, the MC/GCE could be used.
Experimental procedureA 0.1 mol l -1 phosphate buffer solution (pH = 7.2) was used as the supporting electrolyte for the determination of DA and AA...