JBNBJournal of Biomaterials and Nanobiotechnology2158-7027Scientific Research Publishing10.4236/jbnb.2012.31005JBNB-17001ArticlesBiomedical&Life Sciences Chemistry&Materials Science Electrochemical Characterization of Streptavidin-HRP Immobilized on Multiwall Carbon Nanotubes for Biosensor Applications meneHafaiedhHamdiBaccarTahaKtariAdnaneAbdelghani1*Nanotechnology Laboratory, National Institute of Applied Science and Technology, Tunis, Tunisia* E-mail:aabdelghan@yahoo.fr(AA);0501201103013136October 17th, 2011November 24th, 2011 December 6th, 2011© Copyright 2014 by authors and Scientific Research Publishing Inc. 2014This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/

In this work, we used gold labeled multiwall carbons nanotubes for peroxidase biosensor. The gold labeling on multiwall carbon nanotubes can be achieved with Pressure vapor Deposition (PVD) technique. The obtained carbon nanotubes can be immobilized on gold electrode with the airbrushing technique. The stability and the molecular structure of the labeled multiwall carbon nanotubes were characterized with cyclic voltammetry, impedance spectroscopy and Fourrier Transform Infra-Red spectroscopy (FTIR). It shows a higher conductivity and a good stability in water interface. For streptavidin-HRP immobilization, the labeled gold nanotubes were activated over night with thiol-acid (16 carbons). An activation procedure was achieved with EDC/NHS for HRP-streptavidin immobilization. The development of biosensor for H 2O 2 detection was observed with the impedance spectroscopy and cyclic voltammetry techniques. This method could be used to determine total H 2O 2 concentration in the range 4 μM - 160 μM. The results show that the biosensor response depends on the conductivity and the large surface-to-volume ratio attained with multiwall carbon nanotubes. The response of the developed biosensors was reproducible with higher stability.

Carbon Nanotubes; Biosensor; Impedance Spectroscopy; Cyclic Voltammetry1. Introduction

Carbon nanotubes (CNT) have become the subject of intense investigation since their discovery [1]. Such considerable interest reflects the unique behavior of CNT, including their remarkable electrical, chemical, mechanical and structural properties. CNT can display metallic, semiconducting and superconducting electron transport process [2]. CNT can be made by chemical vapor deposition, carbon arc methods, or laser evaporation and can be divided into single wall carbon-nanotubes (SWCNT) and multi-wall carbon nanotubes (MWCNT). SWCNT possess a cylindrical nanostructure (with a high aspect ratio), formed by rolling up a single graphite sheet into a tube [3]. MWCNT comprise of several layers of graphene cylinders that are concentrically nested like rings of a tree trunk (with an interlayer spacing of 3.4 Å) [2,3]. The unique properties of carbon nanotubes make them extremely attractive for the task of chemical sensors, in general and electrochemical detection, in particular [3]. CNTmodified electrodes have been shown useful to accumulate important biomolecules (DNA, antibody) [3] to increase the surface/volume ratio. As an extension of the usual functionalized multiwall carbon nanotubes (-COOH-NH2), they can be decorated with metal nanoparticles. Since metal clusters show a wide range of advanced physic-chemical properties (e.g. high catalytic activity, adsorption capacity, efficient charge transfer, etc. ···) [4]. In this work, we used gold labeled multiwall carbon nanotubes for peroxidase biosensor. The multiwall carbon nanotubes can be immobilized on gold electrode with the airbrushing technique. The stability and the molecular structure of the metal labeled multiwall carbon nanotube were characterized with cyclic voltammetry, impedance spectroscopy and Fourrier Transform Infra-Red spectroscopy (FTIR). It shows a higher conductivity and a good stability in water interface. For streptavidin-HRP immobilization, the labeled gold nanotubes were activated over night with thiol-acid (16 carbons). An activation procedure was achieved with EDC/NHS for HRP-streptavidin immobilization. The development of biosensor for the enzymatic determination of H2O2 was observed with the impedance spectroscopy and cyclic voltammetry techniques. This method could be used to determine total H2O2 concentration in the range 4 μM - 160 μM. The response of the developed biosensors was reproducible with higher stability.

2. Materials and Methods2.1. Reagents

All other materials, including thiol-acid (16-mercaptohexadecanoic acid) (Sigma-Aldrich), 1-ethyl-3-(3-(dimethylamino)-propyl)carbodiimide (EDC) (Aldrich), and Nhydroxy succinimide (NHS) (Aldrich) were used as supplied. The gold labeling MWCNTs (Nanocyl, Belgium) were grown by PVD (Pressure Vapor Deposition) with purity higher than 95%. Nanotubes were up to 50 micrometer in length and their outer and inner diameters ranged from 3 nm to 15 nm and 3 nm to 7 nm, respectively.

The buffer solution used for all experiments was phosphate buffered saline (PBS) containing 140 mM NaCl, 2.7 mM KCl, 0.1 mM Na2HPO4, 1.8 mM KH2PO4, pH = 7 and the redox couple at a 5 mM concentration. All reagents were of analytical grade and ultrapure water (resistance 18.2 MΩ·cm−1) produced by a MilliporeMilli-Q system was used.

2.2. Gold Cleaning and Functionalization

The gold electrodes (1 cm × 1 cm) fabricated at the National Center of Microelectronics of Barcelona (Spain). Evaporated gold (~300 nm thickness) was deposited on silicon, using a titanium underlayer (~30 nm thickness) as substrate. Before modification, the gold electrodes were cleaned in acetone solution for 10 min with ultrasonic bath. After that, they were dried under a nitrogen flow and then dipped for 10 min into “piranha solution” 7:3 (v/v) 96% H2SO4/30% H2O2. Finally, the gold substrates were rinsed 2 to 3 times with ultra-pure water and immediately immersed in an ethanol solution. After cleaning, the gold labeled multiwall carbon nanotubes was dissolved in acetone and deposited on gold electrode with the Airbrushing technique at 90˚C [5]. Immediately after, the substrate was treated for two hours at 120˚C. More details concerning the synthesis and deposition of the gold labeled multiwall carbon nanotubes can be found in reference [6].

After, the gold electrode was immersed in a solution containing 1 mM of Carboxyl thiol (16 carbons) in PBS buffer for 12 hours at room temperature. The gold labeling the outer surface of the carbon nanotubes will react specifically with the thiol. The treated electrode was then immersed in a solution of EDC (0.4 mM) and NHS (0.1 mM) for 1 h. A 10 μl of HRP solution with a concentration of 100 bμg/ml was deposited on the treated electrode for 1 hour. Then, a 10 μl of 1% BSA solution was added on the substrate for 30 min to block the free spaces between the enzyme and the thiol.

2.3. Electrochemical Set-Up2.3.1. Cyclic Voltammetry

Cyclic voltammetry was performed at room temperature in a conventional voltammetric cell with a three electrode configuration using Autolab impedance anlayzer (Ecochemie, Netherland). The gold electrode (0.16 cm2) was used as working electrode, platinum (1 cm2) and Ag/AgCl electrodes were used as counter and reference electrodes respectively. All the electrochemical measurement were carried out in PBS at pH 7.0 with 5 mM and in Faraday cage.

2.3.2. Impedance Spectroscopy

The impedance analysis was performed with the Autolab 302 N impedance analyzer (Eco-Chemie, Netherland) in the frequency range 0.05 Hz - 100 kHz, using a modulation voltage of 10 mV. More details on electrochemical impedance spectroscopy can be found in reference [7- 15].

2.3.3. Fourier Transform Infra-Red Spectroscopy

To confirm the immobilization of metal labeled multiwall carbon nanotubes on gold surface, we used an ATRFTIR spectrometer (BRUKER-IFS-66V/S) equipped with a Germanium (Ge) monoreflection prism with a fixed incident angle of 45˚ and a DTGS detector. All spectra were recorded at 4 cm−1 resolution with 128 scans, from 400 cm−1 to 4000 cm−1. Our method consisted on recording the spectrum of the cleaned gold substrate and then the gold substrate with MCWNTs film. The spectrum of the cleaned electrode served as a reference. The ratio of the two spectra gave the spectrum of the MCWNTs.

3. Results and Discussions3.1. Characterization of Gold Labeled Multiwall Carbon Nanotubes Layer3.1.1. Cyclic Voltammetry

Cyclic voltammetry is an electrochemical technique which can be used to study the kinetic of redox reactions of materials, their insulating and conducting properties. Cyclic voltammograms of the gold electrode (Figure 1(a)) shows a reversible wave which is the typical behavior of gold surface in the presence of the redox couple.

As is shown in Figure 1(a), the cyclic voltammogram defines the characteristics of a diffusion controlled redox process observed at the cleaned bare gold electrode. After modification of the gold surface with the gold labeled multiwall carbon nanotube layer, the current increase due to the high conductivity properties of the MWCNTs layer (Figure 1(b)). The success immobilization of multiwall carbon nanotube layer was confirmed with the current increase.

3.1.2. Impedance Measurement

Electrochemical Impedance Spectroscopy (EIS) is an effective tool for probing the feature surface-modified electrode while controlling its electrical properties [7-15]. This technique was used for example for the characterization of impedance behavior of SAM modified gold electrode [10-15]. Figure 2 shows Nyquist plots for gold electrode before and after MWCNTs deposition at 0 V with redox couple, where Re (z) is the real part and Im (z) is the imaginary part of the complex impedance Z.

The diameter of semi-circle corresponds to the charge transfer resistance of the electrode/electrolyte interface. The impedance spectra should be fitted using the electric model presented in Figure 3.

The capacitance C2 is the double layer capacitance of the gold/electrolyte interface, R1 is the charge transfer resistance in low frequency range and Zw is the impedance due to the mass transfer of the redox species to the electrode described by Warburg. The resistance in high frequency ranges R0 is the resistance of the electrolyte, the contacts and connections.

The decrease of the charge transfer resistance after MWCNTs immobilization (Figure 2(b)) is due to the higher conductivity increases at the gold-electrolyte interface. This confirms the results obtained with cyclic voltammetry. The charge transfer resistance before and after MCWNTs deposition were extracted from the fitted data (Table 1).

3.1.3. FTIR

The infrared absorption spectra of gold electrode without and with MCWNTs are showed in Figure 4. Two main bands at 2900 cm−1 and 2984 cm−1 are clearly observed in the high frequency region.

These are assigned to the symmetric mode and the antisymmetric mode of CH2 respectively. The peaks located at 885 cm−1, 1061 cm−1, 1243 cm−1 and 1400 cm−1 should be assigned to C-H out-of-plane deformation, CH out of plane ring deformation, C-C out-of-plane ring deformation and CH2 scissor vibration mode respectively. This is confirming the deposition of MCWNTs on gold surface.

3.2. Characterization of Self Assembled Monolayers (SAMs) Deposited on Gold Labeled Multiwall Carbon Nanotubes for HRP-Streptavidin Immobilization3.2.1. Cyclic Voltammetry

Figure 5 shows the cyclic voltammograms of the gold electrode with MWCNTs before (Figure 5(a)) and after thiol deposition (Figure 5(b)).

The current decreases due to the high insulating properties of thiol layer. This is confirming the success deposition of thiol on gold labeling MWCNTs. The same behavior was obtained after streptavidin-HRP immobilization (Figure 5(c)).

3.2.2. Impedance Spectroscopy

Figure 6 shows the Nyquist impedance plots for gold electrode with MWCNTs before (Figure 6(a)) and after thiol deposition (Figure 6(b)) at 0 V.

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