journal article·2014-02

Dopamine detection using a patch-clamp system on a planar microeletrode array electrodeposited by polypyrrole/graphene nanocomposites

Li Wang, TingJun Jiang, YiLin Song, WenTao Shi, XinXia Cai

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Abstract

To achieve a dopamine (DA) response with high sensitivity and high signal-to-noise ratio (S/N) with a patch-clamp system, polypyrrole/graphene (PPy/GR) nanocomposites were steadily electrodeposited by an electrochemical method on a planar microelectrode array (pMEA) fabricated by a standard micromachining process. The electrodeposition process was carried out by chronopotentimetry measurement scanning from 0.1 to 0.8 C/cm2 at the current of 2 mA; 0.5 C/cm2 was found to be optimal. The pMEA modified by PPy/GR at the 0.5 C/cm2 exhibits remarkable properties; for instance, the standard deviation (SD) decreases from 8.4614×10−11 to 5.62×10−11 A, reduced by 33.52%, and the sensitivity increases from 2566.88 to 76114.65 μAmMcm−2, 29.65 times higher than the bare Pt (platinum). A good linear relationship between the current and DA concentration in the range of 0.30 to 61.71 μm was obtained, with a correlation coefficient of 0.997. The sensor is meaningful for neuroscience research and the treatment of neurological diseases.
Source: openaire · Quality: candidate unverified · Source record ↗

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OpenAlex topics: Electrochemical sensors and biosensors · Conducting polymers and applications · Electrochemical Analysis and Applications

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References (25)

Show source-provided references
1. Sokoloff P, Giros B, Martres M P, et al. Molecular cloning and characterization of a novel dopamine receptor (D3) as a target for neuroleptics. Nature, 1990, 347: 146–15110.1038/347146a0 ↗
2. Chen W L, Yin P B, Ye W L, et al. Toosendanin-induced change of dopamine level detected by microdialysis in vivo at rat striatum. Chin Sci Bull, 1999, 44: 1106–111010.1007/BF02886136 ↗
3. Lin Y H, Chen C, Wang C Y, et al. Silver nanoprobe for sensitive and selective colorimetric detection of dopamine via robust Agcatechol interaction. Chem Commun, 2011, 47: 1181–118310.1039/C0CC03700A ↗
4. Fiona M N, Andrea V, Lars F. Changes in cortical dopamine d1 re ceptor binding associated with cognitive training. Science, 323: 800–80210.1126/science.1166102 ↗
5. Kuma M H, Swamy B E K, Reddy S, et al. Synthesis of ZnO and its surfactant based electrode for the simultaneous detection of dopamine and ascorbic acid. Anal Methods, 2013, 5: 735–74010.1039/C2AY26124C ↗
6. Zhou G Z, Wang D, Xu S F. Effect if dopamine system in caudate nucleus on acupuncture analgesia. Chin Sci Bull, 1981, 26: 1043–1047.
7. Satish K, Harit D, Mohan S, et al. Polymer Communication Fibers from polypropylene/nano carbon fiber composites. Polymer, 43: 1701–170310.1016/S0032-3861(01)00744-3 ↗
8. Deng F, Zeng X R, Zou J Z, et al. Synthesis of LiFePO4 in situ vapor-grown carbon fiber (VGCF) composite cathode material via microwave pyrolysis chemical vapor deposition. Chin Sci Bull, 2011, 56: 1832–183510.1007/s11434-010-4273-2 ↗
9. Rodger C, Fong A J, Li W, Ameri H, et al. Flexible parylene-basedmultielectrode array technology for high-density neural stimulation and recording. Sens Actuators B Chem, 2008, 132: 449–46010.1016/j.snb.2007.10.069 ↗
10. Cogan S F, Neural stimulation and recording electrodes. Ann Rev Biomed, 2008, 10: 275–30910.1146/annurev.bioeng.10.061807.160518 ↗
11. Rose T L, Robblee L S. Electrical stimulation with Pt electrodes Electro-chemically safe charge injection limits with 0.2 ms pulses. IEEE Trans Biomed, 1990, 37: 1118–112010.1109/10.61038 ↗
12. Matsue T, Aoki A, Ando E J, et al. Multichannel electrochemical detection system for flow analysis. Anal Chem, 1990, 62: 407–40910.1021/ac00203a018 ↗
13. Wang H, Cai H R, Tai H J. Modulation of presynaptic nAChRs on postsynaptic GABA receptor in optic tectum of juvenile Xenopus Chin Sci Bull, 2003, 48: 417–423
14. Novoselov K S, Geim A K, Morozov S V, et al. Two-dimensional gas of massless Dirac fermions in graphene. Nature, 2005, 438: 197–20010.1038/nature04233 ↗
15. Castro Neto A H, Guinea F, Peres N M R, et al. The electronic properties of graphene. Rev Mod Phys, 2009, 81: 109–16210.1103/RevModPhys.81.109 ↗
16. Zhang H, Fu Q, Cui Y, et al. Fabrication of metal nanoclusters on graphene grown on Ru. Chin Sci Bull. 2009, 54: 2446–245010.1007/s11434-009-0411-0 ↗
17. Geim A K, Graphene: Status and prospects. Science, 2009, 324: 1530–153410.1126/science.1158877 ↗
18. Nair R R, Wu H A, Jayaram P N, et al. Unimpeded permeation of water through helium-leak-tight graphene-based membrane. Science, 335: 442–44410.1126/science.1211694 ↗
19. Zhuang Z J, Li J Y, Xu R, et al. Electrochemical detection of dopamine in the presence of ascorbic acid using overoxidized polypyrrole/graphene modified electrodes. Inter J Electrochem Sci, 2011, 1: 2149–216110.1016/S1452-3981(23)18173-9 ↗
20. Kima Y R, Bong S, Kang Y J, et al. Electrochemical detection of dopamine in the presence of ascorbic acid using graphene modified electrodes. Biosens Bioelectron, 2010, 25: 2366–236910.1016/j.bios.2010.02.031 ↗
21. Zhou X M, Liao Y H, Xing D. Sensitive monitoring of RNA transcription levels using a graphene oxide fluorescence switch. Chin Sci Bull, 2013, 58: 2634–263910.1007/s11434-012-5584-2 ↗
22. Shao Y Y, Wang J, Wu H, et al. Graphene based electrochemical sensors and biosensors. Electroanalysis, 2010, 22: 1027–103610.1002/elan.200900571 ↗
23. Hou S F, Kasner M L., Su S J, Highly sensitive and selective dopamine biosensor fabricated with silanized graphene. J Phys Chem, 2010, 114: 14915–14921
24. Heike E. A brain potential study of preparation for and execution of a task-switch with stimuli that afford only the relevant task. Neuroscience, 2010, 33: 1137–1154
25. Barizuddin S, Liu X, Mathai J C, et al. Automated targeting of cells to electrochemical electrodes using a surface chemistry approach for the measurement of quantal exocytosis. Neuroscience, 2010, 1: 590–597