Antifouling nanoporous diamond membrane for enhanced detection of dopamine in human serum
Source abstract
Abstract
In vivo tracking or in vitro real sample analysis by electrochemistry is one of the most straight and useful methods in biosensor field. However, surface biofouling of electrodes by non-specific protein adsorption is inevitable and usually leads to a decrease in sensitivity. Here, we developed a Nafion-coated porous boron-doped diamond (NAF/pBDD) electrode with hydrophobic nanostructures to minimize the biofouling effect and selectively detect dopamine (DA). Larger active area was obtained by this procedure compared to a bare diamond electrode. The as-prepared electrode shows excellent antifouling property and enrichment capacity toward selective detection of dopamine (DA). The low background current of the BDD electrode and the enhanced signals enables a lower detection limit, 42 nmol L−1, and a wider linear range, 0.1–110 μmol L−1, for determination of DA in human serum. Additionally, the facile modified electrode demonstrated renewable property and long-term stability due to the fact that the antifouling nanostructures belong to its own.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Electrochemical sensors and biosensors · Conducting polymers and applications · Advanced Sensor and Energy Harvesting Materials
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References (74)
Show source-provided references
1. Frost M, Meyerhoff ME (2006) In vivo chemical sensors: tackling biocompatibility. Anal Chem 78:7370. https://doi.org/10.1021/ac069475k10.1021/ac069475k ↗
2. Rong G, Corrie SR, Clark HA (2017) In vivo biosensing: progress and perspectives. ACS Sensors 2:327. https://doi.org/10.1021/acssensors.6b0083410.1021/acssensors.6b00834 ↗
3. Nutt JG, Wooten GF (2005) Diagnosis and initial management of Parkinson’s disease. N Engl J Med 353:1021. https://doi.org/10.1056/NEJMcp04390810.1056/NEJMcp043908 ↗
4. Badgaiyan RD (2013) Detection of dopamine neurotransmission in “real time”. Front Neurosci. https://doi.org/10.3389/fnins.2013.0012510.3389/fnins.2013.00125 ↗
5. Weng J, Xue J, Wang J et al (2005) Gold-cluster sensors formed electrochemically at boron-doped-diamond electrodes: detection of dopamine in the presence of ascorbic acid and thiols. Adv Funct Mater 15:639. https://doi.org/10.1002/adfm.20040004910.1002/adfm.200400049 ↗
6. Tryk DA, Tachibana H, Inoue H, Fujishima A (2007) Boron-doped diamond electrodes: the role of surface termination in the oxidation of dopamine and ascorbic acid. Diam Relat Mater 16:881. https://doi.org/10.1016/j.diamond.2007.02.00210.1016/j.diamond.2007.02.002 ↗
7. Vreeland RF, Atcherley CW, Russell WS et al (2015) Biocompatible PEDOT: nafion composite electrode coatings for selective detection of neurotransmitters in vivo. Anal Chem 87:2600. https://doi.org/10.1021/ac502165f10.1021/ac502165f ↗
8. Wang HS, Li TH, Jia WL, Xu HY (2006) Highly selective and sensitive determination of dopamine using a Nafion/carbon nanotubes coated poly(3-methylthiophene) modified electrode. Biosens Bioelectron 22:664. https://doi.org/10.1016/j.bios.2006.02.00710.1016/j.bios.2006.02.007 ↗
9. Tu NTT, Sy PC, Thien TV et al (2019) Microwave-assisted synthesis and simultaneous electrochemical determination of dopamine and paracetamol using ZIF-67-modified electrode. J Mater Sci 54:11654. https://doi.org/10.1007/s10853-019-03709-z10.1007/s10853-019-03709-z ↗
10. Lin P, Lin CW, Mansour R, Gu F (2013) Improving biocompatibility by surface modification techniques on implantable bioelectronics. Biosens Bioelectron 47:451. https://doi.org/10.1016/j.bios.2013.01.07110.1016/j.bios.2013.01.071 ↗
11. Banerjee I, Pangule RC, Kane RS (2011) Antifouling coatings: recent developments in the design of surfaces that prevent fouling by proteins, bacteria, and marine organisms. Adv Mater 23:690. https://doi.org/10.1002/adma.20100121510.1002/adma.201001215 ↗
12. Liu Y, Wang C, Cai N, Long S, Yu F (2014) Negatively charged gold nanoparticles as an intrinsic peroxidase mimic and their applications in the oxidation of dopamine. J Mater Sci 49:7143. https://doi.org/10.1007/s10853-014-8422-x10.1007/s10853-014-8422-x ↗
13. Wightman RM, May LJ, Michael AC (1988) Detection of dopamine dynamics in the brain. Anal Chem 60:769A. https://doi.org/10.1021/ac00164a00110.1021/ac00164a001 ↗
14. Bhushan B, Jung YC (2011) Natural and biomimetic artificial surfaces for superhydrophobicity, self-cleaning, low adhesion, and drag reduction. Progress Mater Sci 56:1. https://doi.org/10.1016/j.pmatsci.2010.04.00310.1016/j.pmatsci.2010.04.003 ↗
15. Choudhary M, Brink R, Nandi D, Siwal S, Mallick K (2016) Gold nanoparticle within the polymer chain, a multi-functional composite material, for the electrochemical detection of dopamine and the hydrogen atom-mediated reduction of Rhodamine-B, a mechanistic approach. J Mater Sci 52:770. https://doi.org/10.1007/s10853-016-0372-z10.1007/s10853-016-0372-z ↗
16. Mohanan VMA, Kunnummal AK, Biju VMN (2018) Selective electrochemical detection of dopamine based on molecularly imprinted poly(5-amino 8-hydroxy quinoline) immobilized reduced graphene oxide. J Mater Sci 53:10627. https://doi.org/10.1007/s10853-018-2355-810.1007/s10853-018-2355-8 ↗
17. Yang C, Trikantzopoulos E, Nguyen MD et al (2016) Laser treated carbon nanotube yarn microelectrodes for rapid and sensitive detection of dopamine in vivo. ACS Sens 1:508. https://doi.org/10.1021/acssensors.6b0002110.1021/acssensors.6b00021 ↗
18. Zhang M, Liao BQ, Zhou X et al (2015) Effects of hydrophilicity/hydrophobicity of membrane on membrane fouling in a submerged membrane bioreactor. Bioresour Technol 175:59. https://doi.org/10.1016/j.biortech.2014.10.05810.1016/j.biortech.2014.10.058 ↗
19. Mao LQ, Jin JY, Song LN, Yamamoto K, Jin LT (1999) Electrochemical microsensor for in vivo measurements of oxygen based on Nafion and methylviologen modified carbon fiber microelectrode. Electroanalysis 11:499. https://doi.org/10.1002/(SICI)1521-4109(199906)11:7%3c499:AID-ELAN499%3e3.0.CO;2-810.1002/(SICI)1521-4109(199906)11:7<499::AID-ELAN499>3.0.CO;2-8 ↗
20. Feng T, Ji W, Tang Q et al (2019) Low-fouling nanoporous conductive polymer-coated microelectrode for in vivo monitoring of dopamine in the rat brain. Anal Chem 91:10786. https://doi.org/10.1021/acs.analchem.9b0238610.1021/acs.analchem.9b02386 ↗
21. Frost MC, Meyerhoff ME (2015) Real-time monitoring of critical care analytes in the bloodstream with chemical sensors: progress and challenges. Annu Rev Anal Chem (Palo Alto Calif.) 8:171. https://doi.org/10.1146/annurev-anchem-071114-04044310.1146/annurev-anchem-071114-040443 ↗
22. Demuru S, Nela L, Marchack N et al (2018) Scalable nanostructured carbon electrode arrays for enhanced dopamine detection. ACS Sens 3:799. https://doi.org/10.1021/acssensors.8b0004310.1021/acssensors.8b00043 ↗
23. Koc Y, de Mello AJ, McHale G, Newton MI, Roach P, Shirtcliffe NJ (2008) Nano-scale superhydrophobicity: suppression of protein adsorption and promotion of flow-induced detachment. Lab Chip 8:582. https://doi.org/10.1039/b716509a10.1039/b716509a ↗
24. Lee C, Choi C-H, Kim C-JC (2008) Structured surfaces for a giant liquid slip. Phys Rev Lett. https://doi.org/10.1103/PhysRevLett.101.06450110.1103/PhysRevLett.101.064501 ↗
25. Zhou L, Hou H, Wei H et al (2019) In vivo monitoring of oxygen in rat brain by carbon fiber microelectrode modified with antifouling nanoporous membrane. Anal Chem 91:3645. https://doi.org/10.1021/acs.analchem.8b0565810.1021/acs.analchem.8b05658 ↗
26. Jiang T, Qi L, Qin W (2019) Improving the environmental compatibility of marine sensors by surface functionalization with graphene oxide. Anal Chem 91:13268. https://doi.org/10.1021/acs.analchem.9b0397410.1021/acs.analchem.9b03974 ↗
27. Svitkova J, Ignat T, Svorc L, Labuda J, Barek J (2016) Chemical modification of boron-doped diamond electrodes for applications to biosensors and biosensing. Crit Rev Anal Chem 46:248. https://doi.org/10.1080/10408347.2015.108212510.1080/10408347.2015.1082125 ↗
28. Wei M, Sun L-G, Xie Z-Y et al (2008) Selective determination of dopamine on a boron-doped diamond electrode modified with gold nanoparticle/polyelectrolyte-coated polystyrene colloids. Adv Funct Mater 18:1414. https://doi.org/10.1002/adfm.20070109910.1002/adfm.200701099 ↗
29. da Silva RP, Lima AWO, Serrano SHP (2008) Simultaneous voltammetric detection of ascorbic acid, dopamine and uric acid using a pyrolytic graphite electrode modified into dopamine solution. Anal Chim Acta 612:89. https://doi.org/10.1016/j.aca.2008.02.01710.1016/j.aca.2008.02.017 ↗
30. Lian Q, He Z, He Q et al (2014) Simultaneous determination of ascorbic acid, dopamine and uric acid based on tryptophan functionalized graphene. Anal Chim Acta 823:32. https://doi.org/10.1016/j.aca.2014.03.03210.1016/j.aca.2014.03.032 ↗
31. Kondo T, Niwano Y, Tamura A et al (2009) Enhanced electrochemical response in oxidative differential pulse voltammetry of dopamine in the presence of ascorbic acid at carboxyl-terminated boron-doped diamond electrodes. Electrochim Acta 54:2312. https://doi.org/10.1016/j.electacta.2008.10.07310.1016/j.electacta.2008.10.073 ↗
32. Yi S-Y, Chang H-Y, H-h Cho YC, Park SH Lee, Bae Z-U (2007) Resolution of dopamine and ascorbic acid using nickel(II) complex polymer-modified electrodes. J Electroanal Chem 602:217. https://doi.org/10.1016/j.jelechem.2007.01.00110.1016/j.jelechem.2007.01.001 ↗
33. Yang N, Foord JS, Jiang X (2016) Diamond electrochemistry at the nanoscale: a review. Carbon 99:90. https://doi.org/10.1016/j.carbon.2015.11.06110.1016/j.carbon.2015.11.061 ↗
34. Yuan Q, Liu Y, Ye C et al (2018) Highly stable and regenerative graphene-diamond hybrid electrochemical biosensor for fouling target dopamine detection. Biosens Bioelectron 111:117. https://doi.org/10.1016/j.bios.2018.04.00610.1016/j.bios.2018.04.006 ↗
35. Williams OA, Nesladek M, Daenen M et al (2008) Growth, electronic properties and applications of nanodiamond. Diam Relat Mater 17:1080. https://doi.org/10.1016/j.diamond.2008.01.10310.1016/j.diamond.2008.01.103 ↗
36. Krueger A, Lang D (2012) Functionality is key: recent progress in the surface modification of nanodiamond. Adv Func Mater 22:890. https://doi.org/10.1002/adfm.20110267010.1002/adfm.201102670 ↗
37. Mei X, Wei Q, Long H et al (2018) Long-term stability of Au nanoparticle-anchored porous boron-doped diamond hybrid electrode for enhanced dopamine detection. Electrochim Acta 271:84. https://doi.org/10.1016/j.electacta.2018.03.13310.1016/j.electacta.2018.03.133 ↗
38. Puthongkham P, Venton BJ (2019) Nanodiamond coating improves the sensitivity and antifouling properties of carbon fiber microelectrodes. ACS Sens 4:2403. https://doi.org/10.1021/acssensors.9b0099410.1021/acssensors.9b00994 ↗
39. Xu J, Chen Q, Swain GM (1998) Anthraquinonedisulfonate electrochemistry: a comparison of glassy carbon, hydrogenated glassy carbon, highly oriented pyrolytic graphite, and diamond electrodes. Anal Chem 70:3146. https://doi.org/10.1021/ac980066110.1021/ac9800661 ↗
40. Chang AY, Dutta G, Siddiqui S, Arumugam PU (2019) Surface fouling of ultrananocrystalline diamond microelectrodes during dopamine detection: improving lifetime via electrochemical cycling. ACS Chem Neurosci 10:313. https://doi.org/10.1021/acschemneuro.8b0025710.1021/acschemneuro.8b00257 ↗
41. Mei R, Wei Q, Zhu C et al (2019) 3D macroporous boron-doped diamond electrode with interconnected liquid flow channels: a high-efficiency electrochemical degradation of RB-19 dye wastewater under low current. Appl Catal B 245:42010.1016/j.apcatb.2018.12.074 ↗
42. Zeng J, Jean DI, Ji C, Zou S (2012) In situ surface-enhanced Raman spectroscopic studies of nafion adsorption on Au and Pt electrodes. Langmuir 28:957. https://doi.org/10.1021/la203545510.1021/la2035455 ↗
43. Bernard M, Deneuville A, Muret P (2004) Non-destructive determination of the boron concentration of heavily doped metallic diamond thin films from Raman spectroscopy. Diam Relat Mater 13:282. https://doi.org/10.1016/j.diamond.2003.10.05110.1016/j.diamond.2003.10.051 ↗
44. Ramamurti R, Becker M, Schuelke T et al (2008) Boron doped diamond deposited by microwave plasma-assisted CVD at low and high pressures. Diam Relat Mater 17:481. https://doi.org/10.1016/j.diamond.2007.08.04210.1016/j.diamond.2007.08.042 ↗
45. Chai Z, Wang C, Zhang H et al (2010) Nafion-carbon nanocomposite membranes prepared using hydrothermal carbonization for proton-exchange-membrane fuel cells. Adv Func Mater 20:4394. https://doi.org/10.1002/adfm.20100141210.1002/adfm.201001412 ↗
46. Dinesh B, Saraswathi R, Senthil Kumar A (2017) Water based homogenous carbon ink modified electrode as an efficient sensor system for simultaneous detection of ascorbic acid, dopamine and uric acid. Electrochim Acta 233:92. https://doi.org/10.1016/j.electacta.2017.02.13910.1016/j.electacta.2017.02.139 ↗
47. Nicholson RS, Shain I (1964) Theory of stationary electrode polarography. Single scan and cyclic methods applied to reversible, irreversible, and kinetic systems. Anal Chem 36:706. https://doi.org/10.1021/ac60210a00710.1021/ac60210a007 ↗
48. Lavagnini I, Antiochia R, Magno F (2004) An extended method for the practical evaluation of the standard rate constant from cyclic voltammetric data. Electroanalysis 16:505. https://doi.org/10.1002/elan.20030285110.1002/elan.200302851 ↗
49. RJ Klingler, JK Kochi (1980) ChemInform abstract: heterogeneous rates of electron transfer. application of cyclic voltammetric techniques to irreversible electrochemical processes. Chemischer Informationsdienst https://doi.org/10.1002/chin.19804009510.1002/chin.198040095 ↗
50. Randviir EP (2018) A cross examination of electron transfer rate constants for carbon screen-printed electrodes using electrochemical impedance spectroscopy and cyclic voltammetry. Electrochim Acta 286:179. https://doi.org/10.1016/j.electacta.2018.08.02110.1016/j.electacta.2018.08.021 ↗
51. Thakur B, Bernalte E, Smith J, et al (2016) The mediatorless electroanalytical sensing of sulfide utilizing unmodified graphitic electrode. Mater C https://doi.org/10.3390/c202001410.3390/c2020014 ↗
52. Jiang L, Nelson GW, Abda J, Foord JS (2016) Novel modifications to carbon-based electrodes to improve the electrochemical detection of dopamine. ACS Appl Mater Interfaces 8:28338. https://doi.org/10.1021/acsami.6b0387910.1021/acsami.6b03879 ↗
53. Pruneanu S, Biris AR, Pogacean F et al (2015) The influence of uric and ascorbic acid on the electrochemical detection of dopamine using graphene-modified electrodes. Electrochim Acta 154:197. https://doi.org/10.1016/j.electacta.2014.12.04610.1016/j.electacta.2014.12.046 ↗
54. Plowman BJ, Mahajan M, O’Mullane AP, Bhargava SK (2010) Electrochemical detection of dopamine and cytochrome c at a nanostructured gold electrode. Electrochim Acta 55:8953. https://doi.org/10.1016/j.electacta.2010.08.04510.1016/j.electacta.2010.08.045 ↗
55. Currie LA (1999) Nomenclature in evaluation of analytical methods including detection and quantification capabilities. Anal Chim Acta 391:105. https://doi.org/10.1016/S0003-2670(99)00104-X10.1016/S0003-2670(99)00104-X ↗
56. Reymond MJ, Speciale SG, Porter JCJE (1983) Dopamine in plasma of lateral and medial hypophysial portal vessels: evidence for regional variation in the release of hypothalamic dopamine into hypophysial portal blood. Endocrinology 112:195810.1210/endo-112-6-1958 ↗
57. Sun CL, Lee HH, Yang JM, Wu CC (2011) The simultaneous electrochemical detection of ascorbic acid, dopamine, and uric acid using graphene/size-selected Pt nanocomposites. Biosens Bioelectron 26:3450. https://doi.org/10.1016/j.bios.2011.01.02310.1016/j.bios.2011.01.023 ↗
58. Ping J, Wu J, Wang Y, Ying Y (2012) Simultaneous determination of ascorbic acid, dopamine and uric acid using high-performance screen-printed graphene electrode. Biosens Bioelectron 34:70. https://doi.org/10.1016/j.bios.2012.01.01610.1016/j.bios.2012.01.016 ↗
59. Manivel P, Dhakshnamoorthy M, Balamurugan A, Ponpandian N, Mangalaraj D, Viswanathan C (2013) Conducting polyaniline-graphene oxide fibrous nanocomposites: preparation, characterization and simultaneous electrochemical detection of ascorbic acid, dopamine and uric acid. RSC Adv. https://doi.org/10.1039/c3ra42322k10.1039/c3ra42322k ↗
60. Jiang J, Du X (2014) Sensitive electrochemical sensors for simultaneous determination of ascorbic acid, dopamine, and uric acid based on Au@Pd-reduced graphene oxide nanocomposites. Nanoscale 6:11303. https://doi.org/10.1039/c4nr01774a10.1039/c4nr01774a ↗
61. Zhang X, Zhang Y-C, Ma L-X (2016) One-pot facile fabrication of graphene-zinc oxide composite and its enhanced sensitivity for simultaneous electrochemical detection of ascorbic acid, dopamine and uric acid. Sensors Actuat B: Chem 227:488. https://doi.org/10.1016/j.snb.2015.12.07310.1016/j.snb.2015.12.073 ↗
62. Bao Y, Song J, Mao Y et al (2011) Graphene oxide-templated polyaniline microsheets toward simultaneous electrochemical determination of AA/DA/UA. Electroanalysis 23:878. https://doi.org/10.1002/elan.20100060710.1002/elan.201000607 ↗
63. Sheng ZH, Zheng XQ, Xu JY, Bao WJ, Wang FB, Xia XH (2012) Electrochemical sensor based on nitrogen doped graphene: simultaneous determination of ascorbic acid, dopamine and uric acid. Biosens Bioelectron 34:125. https://doi.org/10.1016/j.bios.2012.01.03010.1016/j.bios.2012.01.030 ↗
64. Noroozifar M, Khorasani-Motlagh M, Akbari R, Bemanadi Parizi M (2011) Simultaneous and sensitive determination of a quaternary mixture of AA, DA, UA and Trp using a modified GCE by iron ion-doped natrolite zeolite-multiwall carbon nanotube. Biosens Bioelectron 28:56. https://doi.org/10.1016/j.bios.2011.06.04210.1016/j.bios.2011.06.042 ↗
65. Cui R, Wang X, Zhang G, Wang C (2012) Simultaneous determination of dopamine, ascorbic acid, and uric acid using helical carbon nanotubes modified electrode. Sensors Actuat B Chem 161:1139. https://doi.org/10.1016/j.snb.2011.11.04010.1016/j.snb.2011.11.040 ↗
66. Ensafi AA, Taei M, Khayamian T, Arabzadeh A (2010) Highly selective determination of ascorbic acid, dopamine, and uric acid by differential pulse voltammetry using poly(sulfonazo III) modified glassy carbon electrode. Sensors and Actuators B: Chemical 147:213. https://doi.org/10.1016/j.snb.2010.02.04810.1016/j.snb.2010.02.048 ↗
67. Tian X, Cheng C, Yuan H et al (2012) Simultaneous determination of L-ascorbic acid, dopamine and uric acid with gold nanoparticles-beta-cyclodextrin-graphene-modified electrode by square wave voltammetry. Talanta 93:79. https://doi.org/10.1016/j.talanta.2012.01.04710.1016/j.talanta.2012.01.047 ↗
68. Hathoot AA, Hassan KM, Essa WA, Abdel-Azzem M (2017) Simultaneous determination of ascorbic acid, uric acid and dopamine at modified electrode based on hybrid nickel hexacyanoferrate/poly(1,5-diaminonaphthalene). J Iran Chem Soc 14:1789. https://doi.org/10.1007/s13738-017-1119-810.1007/s13738-017-1119-8 ↗
69. Aydoğdu Tığ G, Günendi G, Pekyardımcı Ş (2017) A selective sensor based on Au nanoparticles-graphene oxide-poly(2,6-pyridinedicarboxylic acid) composite for simultaneous electrochemical determination of ascorbic acid, dopamine, and uric acid. J Appl Electrochem 47:607. https://doi.org/10.1007/s10800-017-1060-710.1007/s10800-017-1060-7 ↗
70. Filik H, Avan AA, Aydar S (2016) Simultaneous detection of ascorbic acid, dopamine, uric acid and tryptophan with Azure A-interlinked multi-walled carbon nanotube/gold nanoparticles composite modified electrode. Arab J Chem 9:471. https://doi.org/10.1016/j.arabjc.2015.01.01410.1016/j.arabjc.2015.01.014 ↗
71. Vicentini FC, Raymundo-Pereira PA, Janegitz BC, Machado SAS, Fatibello-Filho O (2016) Nanostructured carbon black for simultaneous sensing in biological fluids. Sensors Actuat B Chem 227:610. https://doi.org/10.1016/j.snb.2015.12.09410.1016/j.snb.2015.12.094 ↗
72. Yang C, Wang Y, Jacobs CB, Ivanov IN, Venton BJ (2017) O2 Plasma Etching and Antistatic Gun Surface Modifications for CNT Yarn Microelectrode Improve Sensitivity and Antifouling Properties. Anal Chem 89:5605. https://doi.org/10.1021/acs.analchem.7b0078510.1021/acs.analchem.7b00785 ↗
73. Ruslinda AR, Ishiyama Y, Penmatsa V, Ibori S, Kawarada H (2015) Repulsive effects of hydrophobic diamond thin films on biomolecule detection. Appl Surface Sci 328:314. https://doi.org/10.1016/j.apsusc.2014.12.01110.1016/j.apsusc.2014.12.011 ↗
74. Escobar JV, Garza C, Alonso JC, Castillo R (2013) Super-mercuryphobic and hydrophobic diamond surfaces with hierarchical structures: vanishment of the contact angle hysteresis with mercury. Appl Surface Sci 273:692. https://doi.org/10.1016/j.apsusc.2013.02.11410.1016/j.apsusc.2013.02.114 ↗