Electrochemical Characterization of Silicon-Based Gold Microband Electrode Array and its Application for Labelless T-2/HT-2 Toxin Immunosensing

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Abstract:

Microelectrode arrays (MEAs) are gaining interest in electroanalysis owing to its distinctive voltammetry properties compared to its macro counterparts. Among the MEAs widely fabricated and studied are microdisc array and microband array. We report here the microfabrication of 10 μm microband array (number of band in an array, N=17) and its application in labelless impedimetric sensing of T-2/HT-2 toxin. The microband array has recess depth (i.e. Si3N4 passivation thickness) of 200 nm. Upon fabrication, the device was first characterized via visual inspection and electrochemical analysis. Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) studies were performed in 1 mM ferrocenecarboxylic acid (FCA) in 0.01 M PBS, pH 7.4. At scan rate of 100 mv s-1, cyclic voltammogram for the microband array exhibited a slight peak-shaped CV; and was found to be scan-rate dependent. Experimental limiting current of the microband array (529±7 nA) was slightly lower compared to the calculated theoretical current (632 nA) indicating mixed diffusion profile of the microband array. The device was then employed in immunosensor construction for T-2/HT-2 toxins detection. T-2 mycotoxin and its metabolite (HT-2), are target of concern in the biosensing application due to its lethal toxicity and prominent presence in EU grains industry. Surface functionalization for anti-T-2 monoclonal antibody (mAb) immobilization was first achieved via surface hydroxylation with plasma cleaning and piranha solution treatment, followed by (3-Aminopropyl) triethoxysilane (APTES) silanization and 15 minutes pre-incubation with various concentrations of anti-T-2 toxin mAb in EDC/NHS mixture. The optimal concentrations for anti-T-2 toxin mAb immobilization on the microband array surface was determined at 0.75 mg mL-1. Based on the calibration curve developed in buffer solution system, the functionalized microband array was proven sensitive as it was able to detect T-2/HT-2 toxin at low dynamic working range (0-25 ppb) and limit of quantitation (LOQ) achieved at 4.89 ppb.

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Materials Science Forum (Volume 1055)

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137-146

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March 2022

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© 2022 Trans Tech Publications Ltd. All Rights Reserved

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[1] Sim WC, Kutrakul N, Khunkaewla P, Schulte A., Three-electrode 30–60 μL mini-cell for ecologically conscious analytical voltammetry with common macro-and microelectrodes, ACS Sustainable Chemistry & Engineering. 8(13) (2020) 5082-5090.

DOI: 10.1021/acssuschemeng.9b07034

Google Scholar

[2] Lanyon, Y.H. and D.W.M. Arrigan, Recessed nanoband electrodes fabricated by focused ion beam milling, Sensors and Actuators B: Chemical. 121(1) (2007) 341-347.

DOI: 10.1016/j.snb.2006.11.029

Google Scholar

[3] Fletcher, S. and M.D. Horne, Random assemblies of microelectrodes (RAM™ electrodes) for electrochemical studies, Electrochemistry Communications. 1(10) (1999) 502-512.

DOI: 10.1016/s1388-2481(99)00100-9

Google Scholar

[4] Stulík K, Amatore C, Holub K, Marecek V, Kutner W., Microelectrodes. Definitions, characterization, and applications (Technical report), Pure and Applied Chemistry. 72(8) (2000) 1483-1492.

DOI: 10.1351/pac200072081483

Google Scholar

[5] Arrigan, D.W.M., Nanoelectrodes, nanoelectrode arrays and their applications, Analyst. 129(12) (2004) 1157-1165.

DOI: 10.1039/b415395m

Google Scholar

[6] Huang, X.J., A.M. O'Mahony, and R.G. Compton, Microelectrode Arrays for Electrochemistry: Approaches to Fabrication, Small. 5(7) (2009) 776-788.

DOI: 10.1002/smll.200801593

Google Scholar

[7] Bartlett, P.N. and S.L. Taylor, An accurate microdisc simulation model for recessed microdisc electrodes. Journal of Electroanalytical Chemistry. 453(1–2) (1998) 49-60.

DOI: 10.1016/s0022-0728(98)00242-3

Google Scholar

[8] Beni, V. and D.W.M. Arrigan, Microelectrode arrays and microfabricated devices in electrochemical stripping analysis, Current Analytical Chemistry. 4(3) (2008) 229-241.

DOI: 10.2174/157341108784911406

Google Scholar

[9] Godino N, Borrise X, Munoz FX, Del Campo FJ, Compton RG, Mass transport to nanoelectrode arrays and limitations of the diffusion domain approach: theory and experiment, The Journal of Physical Chemistry C. 113(25) (2009) 11119-11125.

DOI: 10.1021/jp9031354

Google Scholar

[10] Vidal JC, Bonel L, Ezquerra A, Hernández S, Bertolín JR, Cubel C, Castillo JR, Electrochemical affinity biosensors for detection of mycotoxins: A review, Biosensors and Bioelectronics. 49 (2013) 146-158.

DOI: 10.1016/j.bios.2013.05.008

Google Scholar

[11] https://www.allaboutfeed.net/specials/exploring-mycotoxins-across-the-continents/.

Google Scholar

[12] Edwards S, Barrier-Guillot B, Clasen PE, Hietaniemi V, Pettersson H, Emerging issues of HT-2 and T-2 toxins in European cereal production, World Mycotoxin Journal. 2(2) (2009) 173-179.

DOI: 10.3920/wmj2008.1126

Google Scholar

[13] Wannemacher RW, Wiener SL, Sidell FR, Takafuji ET, Franz DR, Trichothecene mycotoxins. Medical aspects of chemical and biological warfare. 6 (1997) 655-676.

Google Scholar

[14] Makun HA, Dutton MF, Njobeh PB, Mwanza M, Kabiru AY. Natural multi-occurrence of mycotoxins in rice from Niger State, Nigeria, Mycotoxin research. 27 (2) (2011) 97-104.

DOI: 10.1007/s12550-010-0080-5

Google Scholar

[15] Said NAM, Twomey K, Ogurtsov VI, Arrigan DW, Herzog G. Fabrication and electrochemical characterization of micro-and nanoelectrode arrays for sensor applications, Journal of Physics: Conference Series. (307) (2011) 012052.

DOI: 10.1088/1742-6596/307/1/012052

Google Scholar

[16] Mohd Said, N.A. Electrochemical biosensor based on microfabricated electrode arrays for life sciences application. PhD Thesis University College Cork. (2014).

Google Scholar

[17] Vashist, S.K., Comparison of 1-Ethyl-3-(3-Dimethylaminopropyl) Carbodiimide Based Strategies to Crosslink Antibodies on Amine-Functionalized Platforms for Immunodiagnostic Applications, Diagnostics. 2(3) (2012) 23-33.

DOI: 10.3390/diagnostics2030023

Google Scholar

[18] Vashist, S.K., A highly-sensitive and rapid Surface Plasmon Resonance immunoassay procedure based on the covalent-orientated immobilization of antibodies, (2011).

DOI: 10.1038/protex.2011.259

Google Scholar

[19] Bond, A.M., K.B. Oldham, and C.G. Zoski, Steady-state voltammetry, Analytica Chimica Acta, 216(0) (1989) 177-230.

DOI: 10.1016/s0003-2670(00)82009-7

Google Scholar

[20] Nagale, M.P. and I. Fritsch, Individually Addressable, Submicrometer Band Electrode Arrays. 2. Electrochemical Characterization. Analytical Chemistry. 70(14) (1998) 2908-2913.

DOI: 10.1021/ac971041p

Google Scholar

[21] Guerrette, J.P., S.J. Percival, and B. Zhang, Voltammetric Behavior of Gold Nanotrench Electrodes, Langmuir. 27 (19) (2011) 12218-12225.

DOI: 10.1021/la2023743

Google Scholar

[22] Amatore C, Pebay C, Sella C, Thouin L, Mass transport at microband electrodes: transient, quasi‐steady‐state, and convective regimes, ChemPhysChem. 13(6) (2012) 1562-1568.

DOI: 10.1002/cphc.201100942

Google Scholar

[23] Wehmeyer, K.R., M.R. Deakin, and R.M. Wightman, Electroanalytical properties of band electrodes of submicrometer width. Analytical Chemistry. 57(9) (1985) 1913-1916.

DOI: 10.1021/ac00286a026

Google Scholar

[24] Kovach PM, Caudill WL, Peters DG, Wightman RM, Faradaic electrochemistry at microcylinder, band, and tubular band electrodes, Journal of electroanalytical chemistry and interfacial electrochemistry. 185(2) (1985) 285-295.

DOI: 10.1016/0368-1874(85)80136-2

Google Scholar

[25] Deakin, M.R., R.M. Wightman, and C.A. Amatore, Electrochemical kinetics at microelectrodes: Part II. Cyclic voltammetry at band electrodes, Journal of Electroanalytical Chemistry and Interfacial Electrochemistry. 215(1–2) (1986) 49-61.

DOI: 10.1016/0022-0728(86)87004-8

Google Scholar

[26] Lisdat, F. and D. Schäfer, The use of electrochemical impedance spectroscopy for biosensing. Analytical and bioanalytical chemistry. 391(5) (2008) 1555-1567.

DOI: 10.1007/s00216-008-1970-7

Google Scholar

[27] Edwards S, Barrier-Guillot B, Clasen PE, Hietaniemi V, Pettersson H., Emerging issues of HT-2 and T-2 toxins in European cereal production, World Mycotoxin Journal. 2(2) (2009) 173-179.

DOI: 10.3920/wmj2008.1126

Google Scholar

[28] Nabok AV, Tsargorodskaya A, Holloway A, Starodub NF, Gojster O, Registration of T-2 mycotoxin with total internal reflection ellipsometry and QCM impedance methods, Biosensors and Bioelectronics. 22(6) (2007) 885-890.

DOI: 10.1016/j.bios.2006.03.010

Google Scholar

[29] Williamson ML, Atha DH, Reeder DJ, Sundaram PV, Anti-T2 monoclonal antibody immobilization on quartz fibers: stability and recognition of T2 mycotoxin, Analytical Letters. 22(4) (1989) 803-816.

DOI: 10.1080/00032718908051368

Google Scholar