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Graphene Oxide based Label Free Ultrasensitive Immunosensor for Lung Cancer Biomarker, hTERT | OMICS International
ISSN: 2155-6210
Journal of Biosensors & Bioelectronics

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Graphene Oxide based Label Free Ultrasensitive Immunosensor for Lung Cancer Biomarker, hTERT

Meenakshi Choudhary1,2, Veeresh Kumar3,4, Anu Singh1, Manoj P. Singh1, Satbir Kaur2, G.B. Reddy4, Renu Pasricha3, Surinder P. Singh3 and Kavita Arora1*

1Advanced Instrumentation Research Facility (AIRF), Jawaharlal Nehru University (JNU), New Mehrauli Road, New Delhi, India

2Department of Human Genetics, Punjabi University, Patiala, Punjab, India

3CSIR-National Physical Laboratory (NPL), Dr. K. S. Krishnan Marg, New Delhi, India

4Department of Physics, Indian Institute of Technology, Hauz Khas, New Delhi, India

*Corresponding Author:
Kavita Arora
Advanced Instrumentation Research Facility (AIRF)
Jawaharlal Nehru University (JNU)
New Mehrauli Road, New Delhi, India
E-mail: [email protected]

Received Date: July 30, 2013; Accepted Date: September 06, 2013; Published Date: September 13, 2013

Citation: Choudhary M, Kumar V, Singh A, Kaur S, Reddy GB, et al. (2013) Graphene Oxide based Label Free Ultrasensitive Immunosensor for Lung Cancer Biomarker, hTERT. J Biosens Bioelectron 4:143. doi: 10.4172/2155-6210.1000143

Copyright: © 2013 Choudhary M, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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We report the fabrication of ultrasensitive Graphene Oxide (GO) based electrochemical immunosensor to detect human telomerase reverse transcriptase (hTERT), a lung cancer biomarker. The immuno-electrode-has been fabricated by covalent immobilization of rabbit anti-hTERT antibodies (Ab) onto GO films on ITO coated glass. The Fourier Transform Infrared (FTIR) spectroscopic studies confirms the presence of diverse organic functional groups (-COOH, -CHO, -OH) of GO, and the binding (anti-hTERT) onto GO/ITO electrode. Interestingly, Scanning Electron Micrographs (SEM) also reveals clear visual surface modification of the GO film by anti-hTERT antibodies and hTERT antigen (Ag). The electrochemical Differential Pulse Voltammetry (DPV) results show that the GO based immunosensor exhibits specificity and low detection upto 10 ag mL-1 (10×10-18 g mL-1) in wide detection range (10 ag mL-1-50 ng mL-1) for hTERT. The immunosensor showed ability to detect hTERT in spiked sputum samples upto 100 fg mL-1 in dynamic detection range of 100 fg mL-1-10 ng mL-1. The enhanced performance of Ab/GO/ITO is attributed to fast electron transfer and efficient loading of Ab on large surface area provided by GO network. The low level detection of hTERT warrants the realization of point-of-care device for early detection of lung/oral cancer through oral fluids


Lung cancer; hTERT; Electrochemical immunosensor; Graphene oxide


GO: Graphene Oxide; ITO: Indium Tin Oxide; Ab: Antibody; hTERT: Human Telomerase Reverse Transcriptase; BSA: Bovine Serum Albumin; AFM: Atomic Force Microscopy; SEM: Scanning Electron Microscopy; XRD: X-Ray Diffraction; CV: Cyclic Voltammetry; DPV: Differential Pulse Voltammetry; TEM: Transmission Electron Microscopy; FTIR: Fluorescence Transmission Infrared Spectroscopy; EDC: 1-Ethyl-3-(3-Dimethylaminopropyl) Carbodiimide; NHS:N-Hydroxysulfosuccinimide; AFP: Alpha Fetoprotein; AuNP: Gold Nanoparticles; GDCS: Graphene Doped Chitosan; PTH: Polymerized Thionine; GCE: Glassy Carbon Electrode; Fc: Ferrocene; Gr: Graphene; TiO2: Titanium Dioxide; GOx: Glucose Oxidase; PBSE: 1-Pyrene-Butanoic Acid Succinimidyl Ester; PSA: Prostate Specifc Antigen; Chi: Chitosan; Py: Pyrrole; M2+: Metal 2+; ANTA: N-Alpha-Bis (Carboxymethyl)-L-Lysine; Si: Silicon; NSE: Neuron Specific Enolase; FET: Field Effect Transistors; SWNT: Single Walled Carbon Nanotubes; GO: Graphene Oxide; Diuron: 3-(3:4-Dichlorophenyl)-1: 1-Dimethylurea; AP: Alkaline Phosphatase; HRP: Horseradish Peroxidase; SWV: Square Wave Voltammetry; fG: Functionalized Graphene; SPE: Screen Printed Electrode; ITO: Indium Tin Oxide; SPCS: Screen-Printed Carbon Strips; ABA-g-SPCE: P-Aminobenzoic Acid Grafted Screen Printed Carbon Electrodes; hTERT: Human Telomerase Reverse Transcriptase

Significance of Research

Unavailability of apposite diagnostic test capable of monitoring early stage progression/relapse of lung cancer is related to its high mortality rate word wide. We report for the first time detection of lung cancer biomarker hTERT (human telomerase reverse transcriptase), using anti-hTERT for fabrication of graphene oxide (a low cost unique multifunctional material) based immunosensor in spiked sputum samples in the dynamic detection range of 100 fg mL-1-10 ng mL-1 in 30 s exposure time. The easy fabrication of above said electrochemical immunosensor warrants the development of low cost and non invasive diagnostics (first and second stages) for lung cancer.


Cancer is a major health problem worldwide, where poor prognosis of the disease significantly contributes to its monstrous nature [1]. Among various type of cancers, lung cancer is the most prevalent in males worldwide and remain a leading cause of cancer related deaths (~18.2%). In year 2008; 16,07,000 cases of lung cancer with 13,75,000 deaths around the globe and 58,000 lung cancer cases with 51,000 deaths in India were reported [2]. One of the major causes of high mortality rates in lung cancer is unavailability of apposite diagnostic test capable of monitoring early stage progression/relapse. About 70% lung cancer cases are diagnosed in advanced stage resulting in poor survival chances. Contemporary methods for lung cancer detection are Computed Tomography (CT) scan, Positron-Emission Tomography (PET) Scan, thoracoscopy, Magnetic Resonance Imaging (MRI), fluorescence bronchoscopy, sputum cytology, mediastinoscopy, needle biopsy (fine needle aspiration), pulmonary function tests, blood tests, immunological methods. However, all these tests identify the cancer at advanced stage and are time consuming, expensive, and require trained manpower [3,4]. In recent years, advances in molecular characterization and identification of newer cancer biomarkers in biological fluids led to immense possibilities of developing the specific assays to detect and monitor the cancer progression/relapse at early stage [5]. Biomarkers like CYFRA-21, Carcinoembryonic antigen, hnRNP A2-B1, MAGE-11, hTERT, D-dimers are reported to have elevated level in biological fluids of lung cancer patients [6]. Among these, elevated expression of human telomerase reverse transcriptase (hTERT) in sputum/saliva is regarded as a hallmark of tumorigenesis [7]. hTERT is the catalytic subunit of telomerase on chromosome 5p 15.33, and is a rate-limiting determinant of the enzymatic activity [8]. Telomerase activity in human cancer is associated with cell immortalization and acquisition of malignancy with majority of normal tissues [9]. Fernandez-Marcelo et al. [10] have shown that 77.8% cases exhibits telomerase activity during 1st stage of lung cancer. The free circulating DNA of human telomerase reverse transcriptase gene (hTERT) has also been found in blood plasma at first and second stages of lung cancer, enabling early stage cancer detection by DNA based tests [11].

Altered protein/biomarker levels are routinely measured using Enzyme-Linked Immunosorbent Assay (ELISA), electrophoretic immunoassay, Radioimmunoassay (RIA) and mass spectrometrybased proteomics [12]. These methods are sensitive, accurate and precise, but required expensive instruments, materials, trained manpower and longer time for detection are major bottlenecks [13]. Immunosensors, a class of biosensors, presents more attractive option because of design simplicity and ease of operation to develop point of care diagnostics. The most critical step for fabrication of immunosensor involves selection of analyte, biological recognition element (i.e. antibodies), and a suitable immobilization matrix (electrode material) for desired transducer system. A variety of immobilization matrices (nanomaterials, polymers, conducting polymers, carbon nanotubes, self-assembled monolayers etc.) and immobilization methods have been used to fabricate electrochemical, optical, mass based transducer systems for fabrication of biosensors [14]. Inert metals, such as platinum or gold and carbon based materials, have been commonly used as electrochemical transducers for biosensors [15]. The low cost carbon paste is regularly used as the electrode material because of simple construction, low background current and ability for surface regeneration. However, the difficulties in reproducing the composition of the pastand leaching of bio-molecule from electrode surface leading to short life time of electrode are the major drawbacks. The genesis of nanomaterials and nanotechnology have made possible to develop highly sensitive and miniaturized biosensors. Carbon nanomaterials (nanoporous carbon, fullerenes, carbon nanotubes, carbon nanofibers) have been used in development of biosensors with enhanced electrochemical properties. Most of carbon based materials considered to be biocompatible, facilitate easy biomolecule immobilization; exhibit reproducible electrochemical behavior, along with extraordinary physico-chemical properties.

Graphene, layer of carbon atoms arranged in a honeycombed network is viewed as a true planar aromatic macromolecule, and a basic building block of other carbon allotropes [16]. Graphene exhibits unusual structural characteristics, electronic flexibility, high planar surface (2630 m2/g), and ballistic conduction of charge carriers [17,18]. As a result of the unique physico-chemical properties, dense cloud of charge carriers confined in atomic thickness; large chemically modifiable surface area, graphene and graphene-based nano-materials have attracted strong interest in bio-electronic devices [19,20].

Graphene oxide (GO), a chemical derivative of graphene, is considered as a promising material for biosensors due to excellent electrochemical properties, biocompatibility, high defect density and the presence of pendant organic functional groups (-OH, -COOH, -CHO) [21]. GO can be electrostatically suspended in water due to the presence of carboxylic (-COOH) groups [22]. The -COOH groups allows easy attachment of various biomolecules, such as protein, enzyme and nucleic acids onto the GO sheets that warrants its use as electrode in the development of immunosensors. Various immunosensors based on varied matrices have been compared on the basis of their performance and are summarized in Table 1.

S. No Immobilization matrix Analyte Label Detection technique Detection range Detection limit Exposure time Ref.
1 Anti-NSE/ SWNT/ GCE NSE AP DPV 0.033 ng mL-1- 2 µg mL-1 0.033 ng mL-1 60 min [38]
2 Anti CA15-3/TH– NPG–Gr/GCE CA 15-3 HRP DPV 5×10-6- 40 U mL-1 5×10-6U mL-1 30 min [39]
3 Anti-estradiol- Biotin/Strept- ABA-g-SPCE Estradiol HRP Amperome try 0.77 pg mL-1- 250 pg mL-1 0.77 pg mL-1 45 min [40]
4 Anti-GH/ disposable SPCS growth hormone Lable free DPV 25 pg  mL-1- 200 pg mL-1 25 pg mL-1 30 min [41]
5 Anti CEA/APTES/ Si-FET CEA Label Free AC lock-in technique 0.2ng mL-1- 114ng mL-1 0.2 ng mL-1 90 min [42]
6 Anti HIgG/Gr nanosheets- AuNP/GCE HIgG HRP DPV 0.05 ng mL-1- 200ngmL-1 0.05 ng mL-1 50 min [43]
7 AntiAFP/AuNP/G DCS/PTH/GCE AFP HRP DPV 0.7 ng mL-1- 10 ng mL-1 0.7 ng mL-1 25 min [44]
8 Anti-CEA/Au-G/ Chi-Fc/nano- TiO2/GCE CEA Label Free CV 3.4 pg mL-1- 80 ng mL-1 3.4 pg  mL-1 10 min [45]
9 anti-D dimer/ poly (py-pyANTA/M2+) /Au D-dimer Label free DPV 100 pg mL-1- 500 ng mL-1 100 pg mL-1 30 min [46]
10 GOx/Gr/AuNPs/C hi/ Gold electrode Glucose Label free CV 180 μM– 14mM 180 μM - [47]
11 GOx/Gr-Chi/GCE Glucose Label free CV 0.02 mM– 12 mM 0.02 mM - [48]
12 Anti-PSA/PBSE/ Gr/polycarbonate surface PSA Label free multimeter resistance test 0.08 ng mL-1- 100 ng mL-1 0.08 ng mL-1 - [49]
13 Anti-diuron/fG- GO/ SPE diuron AP SWV 0.01pg mL-1- 1000 ng mL-1 0.01 pg mL-1 20 min [37]
14 Anti- hTERT/GO/ITO hTERT Label free DPV 10 ag mL-1 – 50 ng mL-1 10 ag mL-1 30 s present study

Table 1: Response characteristics of various immunosensors reported in literature.

Taking into account the early stage expression of hTERT in oral fluids and synergetic thrust from multi-functional GO, we report the fabrication, characterization, optimization and application of anti- hTERT antibodies functionalized graphene oxide based electrochemical immunosensor for detection of lung cancer biomarker hTERT. The efficient and easy detection of hTERT from oral fluid and/or serum may bring a paradigm shift in prognosis and early stage detection of lung cancer.

Experimental Section

Materials and reagents

Graphite powder (99.9%, 325 mesh, Alfa aesar), Sulfuric acid (H2SO4), Potassium permanganate (KMnO3), Hydrogen peroxide (H2O2), Sodium Nitrate (NaNO3), 1-Ethyl-3-(3-dimethyl amino propyl) carbodiimide (EDC), N-hydroxy sulfo succinimide (NHS), Potassium ferricyanide (K3Fe(CN)6), Potassium chloride (KCl), Potassium phosphate monobasic (KH2PO4), Potassium phosphate dibasic (K2HPO4), Sodium chloride (NaCl), Ethanolamine and Indium Tin Oxide (ITO) glass substrates were purchased from Sigma-Aldrich. Antigen hTERT and polyclonal anti-hTERT antibodies generated in rabbit were purchased from Bioss, USA. All the reagents/buffers have been prepared/diluted in sterile pyrogen free water from Nirlife Healthcare, Nirma Ltd. India.

Synthesis of Graphene oxide

GO was prepared by modified hummer’s method [23]. In this process, 1 g of graphite powder and 1 gm sodium nitrate (NaNO3) were dissolved in 46 ml of H2SO4 in an ice bath with continuous stirring. Thereafter, 6 g of KMnO4 flakes were slowly added to the above mixture under stirring, until this solution becomes dark green. This solution was then transferred to 35 ± 5°C water bath and kept on vigorous stirring for one hour, to make a thick past. Further, 96 ml of millipore water was added, and the solution was stirred for 30 min at 90 ± 5°C. To this solution, 200 ml of water was added followed by the slow addition of 6 mL of H2O2 (30%), turning the color of the solution from dark brown to yellow. The warm solution was then filtered and washed with 200 mL of water. The filter cake were then dispersed in water by mechanical agitation and centrifuged for 3-5 times at low (2000 rpm) and high (8000 rpm) speed for 2 and15 min, respectively, and repeated until the supernatant attains neutral pH. The final sediment was re-dispersed in water with sonication using ultrasonic cleaner, giving a solution of exfoliated GO.

Preparation and characterization of GO/ITO electrode and Ab/GO/ITO Immunoelectrode

Scheme 1 shows preparation of Ab/GO/ITO immunoelectrode. 25 μL GO (1 mg mL-1), prepared by modified hummer’s method was deposited onto ITO coated glass (0.6×0.8 cm) via spin coating method. The GO/ITO electrode was exposed to 1:1 mixture of EDC (0.5 M) and NHS (0.1 M) for 15 min to activate the terminal carboxyl group on GO surface to immobilize anti-hTERT (Ab). 25 μl of anti-hTERT antibodies (2 μg mL-1) was spread over the activated surface for 2 h and unbound antibodies were removed by rinsing the electrode with 10 mM PBS. Remaining active sites were blocked using ethanolamine (0.96 M for 5 min) to avoid non specific interactions. GO/ITO electrode and Ab/GO/ITO immuno-electrodes were characterized using Cyclic Voltammetry (CV), Differential Pulse Voltammetry (DPV), X-Ray Diffraction (XRD), Scanning Electron Microscopy (SEM), Fluorescent Transmission Infrared (FT-IR) spectroscopy, Transmission Electron Microscopy (TEM), Atomic Force Microscopy (AFM), etc.


Scheme 1: Fabrication of GO based electrochemical immunosensor.

Response studies of Ab/GO/ITO immunoelectrode

Ab/GO/ITO immuno electrodes were used to study the response behavior for various concentrations of hTERT (10 ag mL-1-50 ng mL-1) and hTERT spiked sputum samples (100 fg mL-1-10 ng mL-1) in 0.05 mM Zobell’s solution prepared with 5 mM PBS in total volume 3 ml, using DPV. The Ab/GO/ITO immuno-electrodes were exposed to various concentrations of hTERT with constant volume of 20 μl for 30 s and washed with PBS before performing DPV electrochemical analysis.


XRD spectra was obtained on BRUKER D8 Advance X-Ray Diffractometer using Cu Kα radiation (λ=1.541Å).

A Raman spectrum was taken on Varian FT Raman. AFM studies of GO were carried on by using AFM-Multimode-V, Veeco in tapping mode. High-Resolution Transmission Electron Microscopy (HR-TEM) images were monitored on a Tecnai G2 F30 S-Twin HRTEM, using an accelerating voltage of 200 kV. The specimens were prepared on a carbon film coated copper grid (400 mesh), and then dried under room temperature. Electrochemical experiments were performed with an Autolab instrument PGSTAT302N (Eco Chemie B.V., Netherlands) by using a conventional three-electrode system. GO coated ITO (0.6×0.8 cm) electrode served as a working electrode, a platinum wire (1.0 mm diameter) as a counter electrode, and an Ag/AgCl electrode (3.0 mm diameter) with saturated KCl solution as a reference electrode. Cyclic Voltammetry (CV) and Differential Pulse Voltammetry (DPV) measurements were carried out in 3 mM Zobell’s solution (3 mM K3Fe(CN)6 and 0.1 M KCl) and 0.05 mM Zobell’s solution prepared in 5 mM phosphate buffer saline (PBS, pH 7.4), respectively, at 25°C with 3 ml working volume. Fourier Transform Infrared (FT-IR) spectra were carried out using a Nicolet 5700 FTIR spectrometer in the frequency range of 400-3800 cm1. Scanninng electron micrographs of modified electrodes were obtained using Zeiss EVO MF10 Scanning electron microscope. Thickness of GO film was obtained using Dektak-150 thickness profiler (Veeco Pvt Ltd.).

Results and Discussion

Scheme 1a-1e describes diagrammatic representation of fabrication of immunosensor for detection of hTERT, a lung cancer biomarker. Pre cleaned bare ITO (Scheme 1a) was used to deposit thin film (~15 nm, Scheme 1b) of GO using simple spin coating method. Then, anti-hTERT (Ab) was covalently immobilized onto GO/ITO surface through EDC-NHS binding chemistry to fabricate the Ab/GO/ITO immunoelectrode, as shown in Scheme 1c. On exposure of prepared immunosensor with test sample antibody-antigen complex formed (Scheme 1d) that results in generation of electrochemical signal (Scheme 1e). The designed immunoelectrode was characterized at each stage of its development using XRD, Raman, AFM, FTIR, CV, SEM and HRTEM (Scheme 1).

Characterization of as synthesized Graphene oxide (GO)

Figure 1A shows XRD spectra of as acquired graphite (curve 1) and GO (curve2), recorded using Cu Kα radiation (λ=1.541Å) on BRUKER D8 Advance X-Ray Diffractometer (Figure 1).


Figure 1: (A) XRD spectra of graphite (curve 1) and GO (curve 2); (B) Raman spectra of as synthesized GO.

Strong diffraction peaks observed at 2θ value of 26.5° for graphite and at 2θ value of 10.5° for GO powder are ascribed to the (002) planes of graphitic structure. The inter-planer spacing d002 of GO and graphite was calculated to be 8.421 Å and 3.36 Å, respectively, which are comparable to the reported results. The increased interlayer spacing for GO compared to graphite is attributed to the presence of various oxide/ epoxide groups and intercalated H2O molecules.

Further, the high value of ID/IG (1.44) from Raman studies reinforce the formation of oxidized sheets of grapheme, i.e. GO, as shown in Figure 1B. Figure 2A shows Atomic Force Microscope (AFM) image of GO film on silicon wafer, in tapping mode. It can be seen that GO nanosheets with lateral dimensions of ~2500 nm with few smaller sheets of ~200 nm are well distributed onto silicon surface. Height profile analysis elucidates that the thickness of single GO sheet is approximately 0.87 nm. Although, it is very difficult to achieve 100% single layer graphene using wet chemical methods, we have achieved sufficiently good distribution of GO nano-sheets by controlling synthesis conditions. It is, therefore, introspected that uniform distribution of nano-sheets contributes towards higher surface area allowing higher loading of biomolecules that will result in improved sensitivity of designed immunoelectrode. Figure 2B shows the TEM micrographs of the chemically synthesized large area GO sheets with multi-layered folded areas. At low magnification, the presence of wrinkles and folds are prevalent that can also be considered as multilayered regions of GO sheet, otherwise, the areas showing the single unfolded sheet are highly transparent. Figure 2C shows the lattice plane of the single layer of GO with interplanar distance of 0.44 nm (4.40 Å), which is more than 0.33 nm (3.30Å) interplanar distance of grapheme, which is credited to the defects present in GO. Figure 2D shows inverse FFT (Fast Fourier Transform) reconstructed image of the lattice images shown in Figure 2C. This image clearly depicts the hexagonal unit cell of the graphitic structure, marked with the outline. Figure 2D shows the Selected Area Diffraction (SAED) pattern from the multi/double sheet region with a superposition of hexagonal patterns rotated by few degrees shows a ring pattern. This angle corresponds to a mis-orientation between multilayered GO sheets; an effect also observed recently in few-layer graphene samples [24]. The diffraction spots match the hexagonal lattice of graphitic structure. The d-spacing given by SAED pattern is 4.3Å. We found the variation in the‘d’ value calculated from XRD and SAED pattern. It can be explained from the fact that the spacing between the layers decreases due to evaporation H2O molecules when electron beam is focused onto the sample under vacuum. The lack of any diffraction spots other than those corresponding to the graphite structure shows that oxygen-containing functional groups present in GO (of which the GO must partly comprise) do not form superlattice type ordered arrays [24]. (Figure 2)


Figure 2: (A) AFM images of the spin coated GO sheets; (B) TEM micrograph showing the spread out GO sheets; (C) HRTEM image showing the lattice image of single GO sheet; (D) IFFT reconstructed image clearly depicting the atomic resolution image of GO, inset shows the SAED pattern from the multilayer region.

Electrochemical activity of GO

To confirm surface modification, electrochemical behavior was analyzed in Zobell’s solution (3 mM K3Fe(CN)6 and 0.1 M KCl), using Cyclic Voltammetry (CV) for both bare ITO and GO/ITO electrodes. As shown in Figure 3A, it is observed that for GO/ITO electrode, the anodic and cathodic peak current decreases slightly as compared to bare ITO surface. In addition, the peak potential separation (ΔEp) between anodic and cathodic peaks increased from 0.215 V to 0.288 V for ITO and GO/ITO, respectively, confirming successful surface modification by GO. To further assess the electrochemical behavior of GO/ITO, CV studies have been carried out at different scan rates in Zobell’s solution. Figure 3B, the CV of GO/ITO electrode in Zobell’s solution as a function of scan rate (0.02-0.16 Vs-1) exhibits significant increase in redox peak current (Ip) with the increase in scan rate. In addition to this, ΔEp ranging from 0.2 V to 0.344 V increases with increase in scan rate indicating the quasi-reversible kinetics of the GO/ITO electrode. The linear relationship in peak current Ip (both Ipc and Ipa) versus square root of scan rate (v1/2), shown in Figure 3C reveals that the electrochemical reaction at the surface of GO/ITO electrode is a diffusion-controlled process [25,26]. The regression coefficient (R2) for linear fit of Ipa and Ipc were calculated to be 0.9660 and 0.9734, respectively.


Figure 3: (A) Cyclic voltammertic (CV) studies of bare ITO and GO/ITO at 0.05 Vs-1 in Zobell’s solution at 25°C; (B) CV of GO/ITO for various scan rates (0.02-0.16 Vs-1) in Zobell’s solution at 25°C; (C) Plot of peak current (Ipa and Ipc) vs square root of scan rate (v1/2); (D) Plot of ΔEp and Nicholson’s kinetic parameter (Ψ) versus reciprocal of square root of scan rate (v-1/2).

The ratio of Ipc/Ipa=1.028 (at 20 mVs-1), which is less than 1.27 ruling out the possibility of an irreversible electron transfer process [27,28]. The value of Ipc/Ipa=1.028 nearly equals to 1 entails that the electron transfer process is quasi-reversible that is approaching towards reversible kinetics. As an approximate case, considering the process to be a reversible at low scan rates, diffusion coefficient ‘D’ has been calculated as 3.3376×10-5 cm2s-1, using Randal-Sevcik equation [29] (1) for planar electrodes.

Ip=(2.69×105)n3/2AD1/2Cv1/2 (1)

Where Ip is the peak current, v is scan rate in Vs-1, A is area of film in cm2 (0.48 cm2 in our case), C is the bulk concentration (here 3 mM for FeCN6-3), ‘n’ is number of electron transfer per molecule in oxidation process (here n=1). The thickness of the film has been found as 15 nm using Dektak-150 thickness profiler (Veeco Pvt Ltd.) (Figure 3).

Figure 3D shows the plot for dimensionless kinetic parameter (Ψ) and ΔEp for GO electrode. Following Nicholson’s working curve [30], the values of dimensionless kinetic parameter Ψ have been calculated from ΔEp and found to be directly proportional to the reciprocal of the square root of scan rate (v-1/2). Using linear fit curve, the value of standard heterogeneous rate constant (k0) has been determined as 1.4×10-3 cms-1 following equation (2):

Ψ= k0 [RT/(nFD)]1/2 v-1/2 (2)

The obtained value of k0 falls in the range of quasi-reversible electron transfer process (5×10-5 cm s-1 ≥ k0 ≥ 2×10-2 cm s-1) in agreement with literature [31]. The redox process for GO is significantly contributing towards improved electron transfer owing to its inherent electron transfer property and rise in values of k0 and diffusion coefficient (D) provide important insight towards this behavior. As compared to literature, value of diffusion coefficient of GO in Zobell’s solution has been improved by one order of magnitude compared to CVD-GO/ graphite oxide [32]. Similarly, improvement in heterogeneous electron transfer rate (k0) for GO clearly insinuates that this favorable rise (both D & k0) for GO/ITO electrode is ascribed to the uniformly distributed GO nano-sheets and their polycrystalline structure. The results indicate that GO films exhibits better electrochemical properties to achieve a stable and robust electrochemical biosensing device. Further, it is introspected that oxygen-containing groups in GO are contributing hydrophilicity and rapid electron transfer where aromatic regions provides active sites for π-π supra-molecular interactions [33].

Fabrication and characterization of GO/ITO and Ab/GO/ ITO immunoelectrodes

Infrared absorbance spectra of graphene oxide and antibody immobilized graphene oxide films in transmission mode are shown in Figure 4A. The FTIR spectrum reveals the characteristic peaks of graphene oxide (curve i) showing the presence of hydroxyl (C-OH, 3050-3800 cm-1) at 3420 cm-1, carboxyl (COOH, 1650-1750 cm-1) at 1747 cm-1, ketonic species (C=O, 1600-1650 cm-1) at 1636 cm-1 and asymmetric vibrational stretching of sp2 hybridized (C=C, 1500-1600 cm-1) at 1545 cm-1. Furthermore, the presence of some overlapped regions such as α-region (lactols, peroxides, dioxolanes, hydroxyls, epoxides, 900-1100 cm-1) at 1020 cm-1 and γ-region (ethers, epoxide, peroxide, ketones, benzoquinonoes, 1280-1500 cm-1) at 1445 cm-1 are attributed to oxidized graphene sheets i.e. GO [34]. It is observed that the intensities of IR peaks get suppressed after immobilization of antibodies onto GO/ITO (curve ii). The emergence of additional strong peak at 1560 cm-1 related to characteristic N-H bending vibrations (1480-1575 cm-1) of amide II due to the presence of anti-hTERT (Ab) confirms the binding of antibodies onto GO/ITO electrode [35] (Figure 4).


Figure 4: (A) FTIR spectrum of GO (curve 1) and Ab/GO/ITO (curve 2) indicating the presence of functional groups; (B-D) SEM images of GO/ITO, Ab/GO/ITO and hTERT/Ab/GO/ITO immunoelectrode along with schematic representation of respective surface modifications on the left side.

Figure 4B-4D depicts the SEM images (Zeiss EVO MA10 Scanning electron microscope) of GO/ITO, Ab/GO/ITO and hTERT/Ab/GO/ ITO surface, respectively at 20 Kx, along with schematic illuminating stepwise morphological changes with fabrication steps. Figure 4B shows a wrinkled/pleated sheet of GO on ITO coated glass slide. Further, GO/ ITO electrode functionalized with Ab contains uniformly distributed globules onto the surface of GO (Figure 4C), confirming the successful immobilization of Ab. Ab/GO/ITO immunoelectrode was exposed to hTERT (specific antigen) to affirm the binding of antigen to the antibodies immobilized on the surface of immunoelectrode. Change in morphology and presence of lighter colored regions can be assigned to binding of antigen (hTERT) onto Ab/GO/ITO surface (Figure 4D).

Electrochemical characterization and response studies of Ab/ GO/ITO immunoelectrode

The CV and DPV studies of immuno-electrode were carried out to identify the specific and non-specific antigen interaction. Figure 5A shows the CV curves of GO/ITO, Ab/GO/ITO and hTERT/Ab/ GO/ITO at scan rate of 50 mV s-1. It is found that after the covalent immobilization of Ab on to GO/ITO electrode, peak current decreases significantly from 2.213×10-4 A to 1.711×10-4A for Ab/GO/ITO surface. Subsequent, observed decrease in peak current to 1.551×10-4A due to binding of hTERT onto surface of Ab/GO/ITO immunoelectrode can be attributed to surface coverage by the protein that masks the electron transfer process [36]. These results are in agreement with the SEM studies revealing successful fabrication of immunoelectrode.


Figure 5: (A) CV studies of GO/ITO, Ab/GO/ITO and hTERT/Ab/GO/ITO in zobell’s solution at 0.05 Vs-1; (B,D) DPV response studies of Ab/GO/ITO immunoelectrode in 0.05 mM K3Fe(CN)6 contained in 5 mM PBS, pH 7.4 at pulse amplitude 0.03 V and pulse width 0.05 s: (B) DPV for various hTERT concentration (10 ag mL-1-50 ng mL-1); (C) Calibration of the immunosensor for hTERT determination; (D) DPV for specific (hTERT) and non-specific antigen (CD-59, MAGE-A11).

DPV response studies of Ab/GO/ITO immunoelectrode carried out for various concentrations (10 ag mL-1-50 ng mL-1) of hTERT with exposure time of 30 s at 25°C are shown in Figure 5B. It is observed that peak current decreases when hTERT binds to the surface of Ab/ GO/ITO immunoelectrode. These observations are in tune with the SEM and CV studies, reconfirming the antigen-antibody interaction onto the immunosensor surface. It is further noted here that the peak current continue to decrease with the increase in the antigen (hTERT) concentration. DPV studies reveal that 50 ng mL-1 hTERT is the surface saturation concentration for Ab/GO/ITO immunoelectrode and beyond this concentration no further decrease in peak current is observed. On the other end, lowest concentration of hTERT capable of bringing decrease in DPV peak height is 10 ag mL-1. Besides this, as shown in Figure 5C, the linear regression equation: Ipa (μA)=14.6986-1.2912 log ChTERT (ag mL-1) with R2=0.99318 is fitting in range of 100 fg mL-1 to 50 ng mL-1 hTERT. The fabricated Ab/GO/ITO immunoelectrode possess remarkable response characteristics showing 106 times improved detection limit with 30 s antigen exposure time [37].

Figure 5D shows DPV response curves of Ab/GO/ITO immunoelectrode exposed to non-specific cancer antigens (CD-59, MAGE-A11) 10 pg mL-1 each, in 5 mM PBS containing 0.05 mM K3Fe(CN)6. Ab/GO/ITO immuno-electrode exhibited remarkable specificity, as there was no appreciable decrease in peak current corresponds to non-specific antigens CD-59 and MAGE-11. hTERT/ Ab/GO/ITO immuno-electrodes were also examined to evaluate the reusability of the immunosensor, using 30 mM NaOH solution (60 s exposure time) to break the antibody–antigen linkage. Interestingly, it was found that regenerated Ab/GO/ITO immunoelectrode showed DPV response similar to the native Ab/GO/ITO. The fabricated immuno-electrode retains 100% signal after four subsequent regeneration cycles and showed decrease in the signal to ~92.5% after 5th regeneration cycle having relative Standard Deviation (SD) of 5.6%. Besides this, Ab/GO/ITO immunoelectrode has been found to retain 100% DPV response signal after 4 weeks of its fabrication when stored in desiccated condition at 4°C. (Figure 5)

Application of the immunoelectrode in hTERT spiked sputum samples

To investigate the implications of fabricated Ab/GO/ITO immunoelectrode for real biological samples, experiments have been performed using spiked sputum samples. Sputum of normal healthy person was collected and centrifuge two times at 3000 rpm for 15 minutes. Clear supernatant was further diluted in PBS (1:4) and used to investigate the response studies of Ab/GO/ITO immunoelectrode at 25°C. It is observed that DPV response slightly shifts to higher potential (Figure 6A), and is ascribed to the binding of certain salts and other non-specific interferents to the immunoelectrode surface. It can be seen that Ab/GO/ITO immunoelectrode is able to detect upto 100 fg mL-1 of hTERT in spiked sputum and peak current continued to decrease till 10 ng mL-1 of hTERT. The linear regression equation: Ipa (μA)=8.83931- 1.10668 log ChTERT (fg mL-1) with R2=0.96173 is fitting in range of 100 fg mL-1 to 10 ng mL-1 for hTERT in spiked sputum (Figure 6B). These results indicate that fabricated electrode exhibited a good analytical performance with spiked sputum samples and has implications for its application to investigate other cancer biomarkers in real biological fluids.


Figure 6: (A) DPV response studies of Ab/GO/ITO immunoelectrode in 0.05 mM K3Fe(CN)6 contained in 5 mM PBS, pH 7.4 at pulse amplitude 0.03 V and pulse width 0.05 s for various hTERT concentration (100 fg mL-1-10 ng mL-1) spiked in sputum; (B) Calibration of the immunosensor for hTERT determination in spiked sputum.

Furthermore, the analytical performance of the fabricated immunoelectrode has been compared with that of various recent immunosensors based on existing literature [38-49], as shown in Table 1. The present immunoelectrode displayed a good performance with considerable specificity and low detection of analytic concentration. The novelties exhibited by the designed immunosensor are attributed to the multifunctional nature and better physicochemical properties of graphene oxide.

Stability, reproducibility and reusability studies of Ab/GO/ ITO immunoelectrode

The stability of the Ab/GO/ITO immunoelectrodes has been evaluated for over a period of one month. The immunoelectrodes were stored at 4°C after fabrication. Stability of the designed electrodes was studied by incubating them with 50 pg ml-1 of hTERT and DPV was performed before and after incubation with hTERT. The activity of the immunosensors was evaluated and found no loss of signal upto 20th day after incubation. After that the signal was decreased slowly. Therefore, the designed electrode is suitable for hTERT analysis up to 20 days. To evaluate the reproducibility of the immunosensors, a series of five immunosensors were prepared for detecting 50 pg mL-1 hTERT. The Relative Standard Deviation (RSD) of the measurements for the five electrodes was 5.3%, suggesting the precision and reproducibility of the immunosensor was quite good. In an effort to evaluate the reusability of the immunosensor, 30 mM NaOH solution was used to break the antibody-antigen linkage. After detecting 2 ng mL-1 of hTERT, the immunosensor was dipped into the NaOH solution for 60 s, and used to detect hTERT again. The immunosensor retained 92.5% of the initial value after 5 regeneration cycles and a RSD of 5.6% was obtained. The good regeneration ability demonstrated by the immunosensor may be attributed to the good stability of the antibody on the electrode surface through covalent binding.


In conclusion, Graphene Oxide prepared from graphite using modified Hummer’s method is successfully used to deposit thin films of GO onto ITO coated glass substrate. An ultrasensitive label free electrochemical immunosensor has been developed by covalent immobilization of anti-hTERT antibody onto GO/ITO. The results indicate that the Ab/GO/ITO immunoelectrode can effectively sense hTERT at low level of concentration upto 10 ag mL-1 with linear detection range of 100 fg mL-1-50 ng mL-1 hTERT. The Ab/GO/ITO electrode showed in the detection of hTERT in spiked sputum samples in the dynamic range of 100 fg mL-1-10 ng mL-1 hTERT, suggesting its potential for real biological fluid samples. Besides this, the immunoelectrode retained its activity after multiple uses. The excellent performance of the immunosensor is ascribed to graphene oxide that provides favorable microenvironment for protein immobilization and promotes direct electron transfer at the electrode surface and larger surface area. The ease of fabrication using low-cost process, the graphene oxide based immunosensor promises for cost effective commercial device for early detection of lung cancer. Further, the compatibility of GO to integrate with MEMS technology could pave the way for the development of miniaturized immunosensors towards point-of -care diagnostics.


We are grateful to Prof. Sopory, Vice Chancellor, JNU; Prof. Madhubala, Director, AIRF, JNU and Prof. Budhani, Director, NPL, New Delhi, India for showing interest in this work. MC is thankful to DBT for providing JRF. Veeresh Kumar is thankful to UGC for providing SRF. Financial support received under the DBTsponsored project IYBA-2008 (BT/B1/12/045/2008) and RGYI-2009 (BT/PR13127/ GBD/27/195/2009) is sincerely acknowledged.


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