Application of Graphene in Biosensors

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The purpose of this Project is to study the synthesis of graphene and application of graphene in biosensors.

To understand the importance of using graphene in building biosensors. And compare the sensitivity detection limit and other criteria of biosensors.

Also to understand various methods used to functionalize antibody and techniques used to build biosensors so that it is biocompatible and miniaturized and easy to use.


1. Introduction

2. Biosensor

2.1 Biosensor system

2.2 Bio receptors

2.3 Applications

3. Graphene

3.1 Properties

3.2 Synthesis

4. Paper-1

5. Paper-2

6. Paper-3

7. Paper-4

8. Paper-5

9. Conclusions

10. References




A biosensor is an intrusive tool, used for the detection of an analyte that combines a biological component with a transducer. The sensitive biological element (e.g. tissue, microorganisms, organelles, cell receptors, enzymes, antibodies, nucleic acids, etc.) is a biologically derived material that interacts (binds or recognizes) with the analyte that are to be detected. The biologically sensitive elements can also be produced by biological engineering. The transducer or the detector element (works in a physicochemical similarly; optical, piezoelectric, electrochemical, etc.) transforms the signal coming from the interaction of the analyte with the biological element into another signal (i.e., transduces) that can be more easily measured or viewed. The biosensor device with the associated electronics or signal processors that are primarily responsible for the display of the signals in a recognizable way. This sometimes results in the most expensive part of the sensor device, however it is possible to generate a user friendly display that includes transducer and sensitive element. The readers are usually designed and manufactured to suit the different working principles of biosensors.

Biosensor system

A biosensor typically consists of a bio-owning accessory, bio transducer accessory, and electronic accessory which include a signal amplifier, processor, and display. Transducers and electronics can be combined, e.g., in CMOS-based micro sensor systems. The recognition component, often called a bio recognizing element, uses biomolecules from organisms or receptors made after biological systems to interact with the analyte to be tested. This interaction is measured by the transducer which outputs a measurable signal proportional in the availability of the target analyte in the sample. The main objective of the design of a biosensor is to facilitate quick, convenient testing at the point of concern or care where the sample was produced.


In a biosensor, the bioreceptor is meant to move with the precise analyte of interest to provide a control measurable by the electrical device. High property for the analyte among a matrix of different chemical or biological parts may be a key demand of the bioreceptor. Whereas the kind of biomolecule used will vary wide, biosensors is classified consistent with common kind bioreceptor interactions involving: antibody/antigen, enzymes/ligands, nucleic acids/DNA, cellular structures/cells, or biomimetic materials.


There are numerous potential utilizations of biosensors of different sorts. The primary necessities for a biosensor way to deal with be significant as far as research and business applications are the recognizable proof of an objective particle, accessibility of a reasonable natural acknowledgment component, and the potential for dispensable convenient identification frameworks to be wanted to touchy lab based strategies in a few circumstances. A few cases are given underneath:

• Glucose observing in diabetes patients

• Other therapeutic wellbeing related targets

• Environmental applications e.g. the discovery of pesticides and stream water contaminants, for example, substantial metal particles.

• Remote detecting of airborne microbes e.g. in counter-bioterrorist exercises

• Remote detecting of water quality in waterfront waters by portraying on the web distinctive parts of shellfish ethology (organic rhythms, development rates, producing or passing records) in gatherings of relinquished bivalves around the globe

• Detection of pathogens

• Determining levels of dangerous substances prior and then afterward bioremediation

• Detection and deciding of organophosphate

• Routine systematic estimation of folic corrosive, biotin, vitamin B12 and pantothenic corrosive as another option to microbiological examine

• Determination of medication buildups in sustenance, for example, anti-infection agents and development promoters, especially meat and nectar.

• Drug revelation and assessment of natural movement of new mixes.

• Protein designing in biosensors

• Detection of dangerous metabolites, for example, mycotoxins.

A typical case of a business biosensor is the blood glucose biosensor, which utilizes the protein glucose oxidase to separate blood glucose. In doing as such it initially oxidizes glucose and utilizations two electrons to lessen the FAD (a segment of the chemical) to FADH2. This thusly is oxidized by the terminal in various strides. The subsequent current is a measure of the grouping of glucose. For this situation, the anode is the transducer and the compound is the naturally dynamic segment.


Graphene is an allotrope of carbon as a two-dimensional nuclear scale, hexagonal lattice .It was synthesized, and described in 2004 by Geim and Novoselov. They won Nobel Prize 2010 in material science for finding graphene synthesis by mechanical investigation. The novel parameters of GN, outstandingly its impressive electron portability, thermal conductivity, high surface area and electrical conductivity, are bringing elevated consideration into biomedical applications. This review evaluates the current advances in GN-based Biosensors and its subsidiaries in various zones to concentrate on glucose detecting, DNA detecting, medication and quality conveyance, growth treatment and other related biomedical applications (electrochemical sensors, tissue building, hemoglobin and cholesterol detecting), together with a short examination on difficulties and future points of view in this quickly creating field.


• High surface region (2630 m2/g).

• Excellent electrical conductivity (1738 S/m).

• Good warm conductivity (5000W/m/K).

• Strong mechanical quality (around 1100 GPa).

• Strong mechanical quality (around 1100 GPa).

• Good thermal conductivity (5000W/m/K)

• High charge bearer versatility (around 10,000 cm2 V−1 s−1).


  • Mechanical exfoliation

Atomic layer of GN can be seen on ∼300 nm SiO2 substrates.

Pristine GN with the highest quality of electrical properties.

The size and thickness are uncontrollable, thus limited practical applications.

  • Liquid-based exfoliation

Graphite powders are initially oxidized by chemical modification to be dispersed in solution.

Large-scale production for bulk applications, i.e. super capacitors, composite materials.

  • Epitaxial growth

A conversion of SiC substrate to GN via sublimation of silicon atoms on the surface. Done at very high temperature (∼1300°C) Accessibility is limited due to high-end equipment.

  • Chemical vapour deposition ( CVD) growth

GN Most promising, inexpensive and feasible method for single-layer GN synthesis.Using transition métal (Ni, Cu, Si) substrats.Can be scaled up for large area GN production for practical applications.

Graphene-based biosensors for detection of bacteria and their metabolic activities


Exhibition of Nano electronic sensor based on antibody-modified chemical-vapor-deposition-grown large-sized graphene to check presence of bacteria (E. coli) with high sensitivity (10 cfu/mL) and specificity. Moreover, the glucose activated metabolic exercises of microscopic organisms can be identified continuously. Such straightforward Nano electronic biosensor could be helpful for fast and name free discovery of microscopic organisms, high throughput measure of their metabolic exercises, and high throughput screening of antibacterial medications.

Experimental section

Growth of graphene film and characterizations

Large measured graphene films were developed on copper foils (AlfaAestar) by chemical vapor deposition (CVD) utilizing ethanol as the Carbon source. Copper foils were stacked into a quartz tubular Furnace, which was then cleansed with unadulterated Ar (1000 sccm) for 10 Min. After raising the heater temperature to 900 0C, the CVD Growth of graphene was begun by coordinating H2/Ar gas blend (20% H2; 40 sccm) with ethanol vapor into the heater at 900 0C.The development proceeded for around 30 min, trailed by chilling off under the H2/Ar climate. The morphology of the graphene surface was described with tapping mode atomic force microscopy (AFM) (Dimension3100, Veeco). Raman spectra were acquired with confocal Raman microscopy utilizing a laser wavelength of 488 nm (WITec CRM200).

Fabrication of graphene device

The as-developed graphene film on copper foil was spin covered with a thin layer of poly-methyl methacrylate (PMMA) mixed in Chlorobenzene, trailed by strengthening at 180 0C for 1 min. The PMMA/graphene films were then discharged from the copper foil by compound scratching of the fundamental Cu in an iron chloride Solution. The suspended film was exchanged to DI water to evacuate the remaining copper etchant and after that grabbed by the Substrate. After the PMMA film was broken down by Acetone, the Sample was washed with bounteous DI water and strengthened at 450 0C For 20 min (H2/Ar climate). Two anodes (source and Drain) were accordingly arranged cross the graphene film (2*4 mm¬2) utilizing silver conductive paint (RS Component). At last, Silicone elastic (Dow Corning) was utilized to protect the terminals and frame the recording chamber.


Functionalization of graphene device


Graphene gadget was hatched with 5 mM linker atom (1-pyrenebutanoic corrosive succinimidyl ester, i-DNA Biotechnology) in dimethylformamide (DMF) for 2 h at room temperature, and washed with unadulterated DMF and DI water. The Linker-changed graphene was then brooded with 50 ppm hostile to E. coli O and K counter acting agent (i-DNA Biotechnology) in Na2CO3-NaHCO3 cushion arrangement (pH 9.0) overnight at 4 0C Followed by washing with DI water and phosphate supported saline arrangement (PBS). At that point, the gadget was brooded with 0.1 M ethanolamine (pH 9.0) for 1 h to extinguish the unreacted succinimidyl ester assemble on linker particles, trailed by 1 h hatching with 0.1% Tween 20 to passivate uncoated graphene.






Electrical measurements

All measurements were conducted under ambient conditions using a semiconductor device analyzer (Agilent, B1500A). Thegraphene device was one-sided at 100 mV, and the gate voltage wasapplied via an Ag/AgCl electrode submerged in the PBS solution on top of the graphene.

Results and discussions-

Extensive measured graphene films were developed on copper foils at 900 0C by chemical vapor deposition (CVD) utilizing ethanol as the carbon source. Subsequent to being exchanged onto the Si/SiO2 substrate, graphene films were described by Raman spectroscopy. Fig. describes the 2 dimensional Raman guide of a graphene film built by plotting the pinnacle width at half tallness of the 2D band in the Raman range. The brighter islands in the Raman outline the few-layered districts while the rest is single-layered graphene. The Raman range taken at a darker spot (demonstrated by a circle in the Raman outline) the trademark range of single-layered graphene with a sharp 2D top and a proportion in the vicinity of 2D and G band (I2D/IG) of 4.0 (strong follow in figure interestingly, the range in a brighter spot (shown by a square) displays a weakened 2D band and a low I2D/IG (0.5), showing its few-layered structure (spotted trace).

To explicitly distinguish microscopic organisms E. coli, hostile to E. Coli antibodies were first moved onto graphene film by means of the linker atoms (1-pyrenebutanoic corrosive succinimidyl ester) whose pyrene group toward one side ties to the graphene surface through solid pi-pi connection and the succinimidyl ester bunch at the flip side covalently responds with the amino gathering on the counter acting agent. To avoid nonspecific authoritative, ethanolamine was connected to evacuate the unreacted succinimidyl esters on the linker particles and Tween 20 was utilized to passivate the uncoated graphene territory.

The CVD-developed graphene displayed the trademark ambipolar field-impact and every functionalization step prompted move in the exchange bend (drain source current Ids versus the arrangement door voltage Vg).

The graphene conductance increments with time because of continuous increment in the quantity of E. coli gotten by the antibodies on the graphene film. As the graphene FET was worked at the p-type region (Vg=0 V), the expansion in graphene conductance is because of expanded gap thickness initiated by the exceptionally contrarily charged bacterial divider.

The gadget reaction achieved the most extreme in around 1 h because of immersion of microbes official (Above Fig. Inset).

It is realized that glucose digestion in microorganisms prompts extracellular condition because of arrival of natural acids (e.g. pyruvic, citrus, and lactic corrosive). We speculated that the release of natural acids into the Nano-hole between the graphene and the interfacing bacterial surface would modify the nearby pH and therefore the graphene conductance. Right off the bat, we checked that our graphene gadget is without a doubt exceptionally delicate to pH Decrease in pH lessens the graphene conductance. This is reliable with the past provide details regarding single-layer graphene. Hostile to E. coli counter acting agent functionalized graphene FET was brooded with E. coli suspension (105 cfu/mL) for 30 min, trailed by PBS wash. As foreseen, a reduction of Ids was watched when glucose was added to the recording chamber. The extent of gadget reaction is relative to the glucose fixation (Fig. upper inset) and glucose was not ready to trigger any reaction from a graphene gadget without microorganisms

(Fig. bring down inset). These perceptions recommend that the watched signals come about because of the glucose-actuated bacterial digestion.



Development of an Amperometric Cholesterol Biosensor Based on Graphene-Pt Nanoparticle Hybrid Material

The improvement of an exceptionally touchy amperometric biosensor in view of the half and half material gotten from nanoscale Pt particles (nPt) and graphene for the detecting of H2O2 and cholesterol. The biosensing stage was created utilizing the half and half material and compounds cholesterol oxidase and cholesterol esterase. Synthetically incorporated graphene has been embellished with Nano estimated Pt particles. The electron minute estimations demonstrate that the Pt nanoparticles on graphene have a normal size of 12 nm and are haphazardly disseminated all through the surface. The Pt nanoparticle based half and half material modified anode efficiently catalyzes the electrochemical oxidation of H2O2 at the capability of 0.4 V, which is >100 mV less positive regarding the mass Pt terminal. The detecting stage is very touchy and shows straight reaction toward H2O2 up to 12 mM with a discovery breaking point of 0.5 nM [S/N (signal to noise proportion) ) 3] without any redox arbiter or catalyst. The blend of electronically very conductive graphene and chemically dynamic Pt nanoparticle favors the encouraged electron exchange for the oxidation of H2O2. The cholesterol biosensor was produced by immobilizing cholesterol oxidase and cholesterol esterase on the surface of graphene-nanoparticle half and half material. The bienzyme incorporated nanostructured stage is extremely delicate, particular toward cholesterol, and it has a quick reaction time. The affectability and farthest point of identification of the cathode toward cholesterol ester are 2.07 (0.1 µA/µM/cm2) and 0.2 µM, separately.

The electrochemical bio detecting of cholesterol can be performed by two diverse methodologies: (i) the enzymatic response of cholesterol with cholesterol oxidase and (ii) interceded bioelectrocatalytic oxidation of cholesterol. In the previous case the convergence of cholesterol can be measured by checking.

The concentration of either H2O2 produced or oxygen expended amid the enzymatic response. Checking the centralization of H2O2 is favored as the exact estimation of the grouping of oxygen is somewhat troublesome. Enzymatically produced H2O2 can be electrochemically measured either by its decrease or oxidation.


Experimental Section


Synthesis of Graphene Nanosheets


Graphene oxide was orchestrated by adjusted Hummer’s method49, 50 by the peeling of graphite. Quickly, 50 mL of concentrated H2SO4 was gradually added to a blend of graphite powder (1 g) and NaNO3 (1 g) in a 500 mL round-base carafe at 0 °C. Strong KMnO4 (6 g) was added to the response vessel, and the blend was mixed consistently for 1 h at room temperature. Water (200 mL) was gradually added to the blend, and the mixing was proceeded for another 15 min. At that point H2O2 arrangement (30%) was added to the response vessel until the gas development was stopped. The subsequent blend was centrifuged in a ultracentrifuge to evacuate shed graphite and oxidizing operators. The deposit was then washed more than once with 5% HCl arrangement until the washing arrangement gave a negative test for the nearness of sulfate particles with BaCl2 arrangement. The deposit acquired after rehashed washing was additionally washed with bountiful measures of Millipore water and dried in vacuum to get the yellow-darker strong of graphene oxide (GO). The graphene nanosheets were acquired from GO by its lessening. GO (200 mg) was scattered in water(150 mL) by sonication for ∼1 h. NaBH4 (400 mg) was added to the GO scattering and blended overwhelmingly for 30 min, and afterward the blend was warmed at 135 °C for ∼6 h for the entire change of GO to graphene. Amid the expansion of NaBH4, the yellow-darker shade of the response blend swings to dark.

The dark shaded graphene was detached by centrifugation and washed over and again with Millipore water and air-dried and subjected for different estimations.

Introduction of Pt Nanoparticles


1. 5 mL of solution of GNS (1 mg/mL of water) was mixed very well with H2PtCl6 ·6H2O (1 mM), and the suspension was kept for 1 h at room temperature. To this mixture 0.2 mL of 0.08% NaBH4 was mixed, and the mixture was stirred in room temperature for 12 h.

3. Graphene-Pt (GNS-nPt) nanoparticle hybrid material was collected by centrifuging with an ultracentrifuge.

Development of the Biosensing Platform.

1. GC electrode was used as a conducting substrate.

2. GNS-nPt hybrid material (1 mg) was mixed with 3% ethanolic nafion (NF) solution and sonicated for 5 min to get a homogeneous dispersion. This suspension (5 μL) was drop-cast on the cleaned GC electrode and dried at room temperature for 12 hours.

3. The enzyme mixture (3 μL) (cholesterol oxidase and cholesterol esterase in 2:1 ratio) was drop-cast on the GNS-nPt electrode and dried at 4 °C for 6 h.

Results and discussions-

Characterization of GO, GNS, and GNSnPt.

1. The oxygen functionalities of GO show characteristic peaks at 3400 (υstr of O-H), 1725 (υstr of C=O), 1620 (υstr of C=C), and 1225 cm-1

(Epoxy symmetrical ring deformation vibration) (Figure below).

The intensity of all  these peaks significantly reduced, and some

of the peaks are totally vanished, when GO was chemically reduced to GNS. A new peak at 1548 cm-1 due to the skeletal vibration of GNS.

2. The Raman spectra of GO demonstrates the D and G groups at 1370 and 1605 cm-1, separately. The substance lessening of GO is known to move these groups to bring down wavenumber and improve the proportion of the power of the D band to G band (ID/IG). Of course, these groups move to 1356 and 1586 cm-1 and the ID/IG esteem increments to 1.14 from 0.88 (Figure above). The critical upgrade in the proportion of GNS shows the lessening in the normal size of the sp2 endless supply of the shed GO. Additionally, the Raman range of GNS demonstrates the trademark 2D band at 2730 cm-1 and the S3 band at 2943 cm-1. The UV-vis retention range of GO demonstrates a principle band at 234 nm and a shoulder band at 300 nm relating to the π-π* move of fragrant C-C and C=O securities, separately.

3. The GNS and GNS-nPt cathodes were additionally portrayed by measuring the capacitance and their voltammetric and electrochemical impedance reaction toward the outer redox test [Fe(CN)6]3-in 0.1 M PBS. The capacitance of the terminals was measured at the capability of 0.4 V in unbiased pH. Obviously, expansive capacitance was watched for the GNS anode. In any case, the capacitance of the GNS-nPt cathode is ∼10 times lower than that of the GNS terminal (Supporting Information). It is intriguing to note that the enhancement of GNS with nPts altogether impacts the capacitance.

4. The GNS-nPt anode indicates all around characterized voltammetric reaction for the oxidation of H2O2 at the capability of 0.4 V, which is fundamentally less positive than that of the GNS terminal (Figure beneath). Slow increment in the voltammetric top current was seen while expanding the grouping of H2O2, and the adjustment plot is direct for a wide fixation go (Supporting Information). The oxidation of H2O2 on the GNS terminal happens at the capability of 0.6 V, and the voltammetric reaction is somewhat drowsy, apparently because of the moderate electron-exchange







Biosensing of Cholesterol

Two types of sensors were developed:

(i) A biosensor for free cholesterol using the enzyme ChOx and

(ii) A biosensor for total cholesterol using the enzymes ChOx and ChEt.

6. The response was linear up to the concentration of 35 μM, and the lowest concentration of cholesterol ester detected was 0.2 μM.

The sensitivity of the biosensor toward cholesterol and cholesterol ester was 1.43 ± 0.1 and 2.07 ± 0.1 μA/μM/cm2, respectively.

A DNA biosensor based on graphene paste electrode modified with Prussian blue and chitosan


A synthetically changed graphene paste cathode was set up by joining fitting measures of graphene in a paste blend, trailed by electrodepositing Prussian blue (PB) and covering chitosan on the terminal surface. The cathode could tie ssDNA, and gave a superior voltammetric reaction for supplement DNA than did common carbon paste terminals. The reaction of the cathode was portrayed as for the paste sythesis, immobilization time of test DNA on the chitosan and PB changed graphene glue anode, and the impact of 1-ethyl-3-(3-dimethylaminopropyl)- carbodiimide hydrochloride (EDC). The electrochemical conduct of PB collected on the graphene paste anode was examined. The blend of graphene and PB can improve the present reaction of the graphene paste anode.

Experimental Section

Twenty-four-base synthetic oligonucleotides were purchased from Invitrogen Bioengineering Ltd. Company (Shanghai, China):



Three mismatch-containing sequence (mcDNA): 50-TCG TCC TGA AAC GTT GCG CCT CTC-30

Noncomplementary DNA (ncDNA): 50-GAG CGG CGC



Preparation of graphene

  1. Graphite powders were first oxidized by potassium chlorate in the presence of concentrated nitric acid and sulfuric acid for 120 h.
  2. After oxidation of graphite, the mixture was added to excess water, washed with a 5% solution of HCl.

3. Washed with water until the pH of the filtrate was neutral.

4. The oxidized graphite was then suspended in a mixture of ethanol and water followed by ultra-sonication for 1h.The exfoliated graphite oxidation was reduced to graphene Nano platelets by hydroquinone for 20 h.

Preparation of electrode

1. GPE was set up by blending graphene and Nujol oil at various proportions. The paste was painstakingly hand-blended in a mortar and after that stuffed into one end of a Teflon tube (4 mm bore, 1 mm divider thickness). The electrical contact was given by a copper wire associated with the glue in the internal gap of the tube.

2. The surface of the subsequent paste anode was cleaned on straightforward paper until the surface had a sparkling appearance. The anode was flushed precisely with water preceding every estimation.

3.The PB film was electrodeposited as follows:30 the GPE was embedded in a fluid arrangement comprising of 2 mMFeCl3, 2mM K3[Fe(CN)6], 0.1 M KCl, 0.1 M HCl and a steady capability of +0.4 V (versus SCE) was connected for 120 s. The anode was then precisely washed with water and moved into the supporting electrolyte arrangement containing 0.1MKCl and 0.1MHCl, where the cathode was cycled 20 times in the vicinity of 0.05 and +0.35 V at a sweep rate of 40 mV s-1, washed with water, and afterward dried with nitrogen (signified as PB/GPE).

DNA immobilization on the Chit/PB modified GPE


The Chit/PB/GPE was submerged in 10 mM phosphate cradle (pH 7.3) containing 2.12_10_5Moligonucleotide and 0.1MEDC for 10 h with mixing at room temperature. The oligonucleotide test was immobilized through the arrangement of phosphoramidate bonds between the amino gathering of Chit and phosphate gathering of the oligonucleotides at the 50 end, under the impact of EDC, on the surface of the altered anode. At long last, the terminal was washed with water a few times to evacuate the unbound DNA tests. After DNA was immobilized on the cathode, the subsequent terminal was signified as ssDNA/Chit/PB/GPE.

the surface of the PB altered GPE and dried in air to shape a layer of Chit film

Results and discussion-

The conductivity of the GPE material influences the electrochemical expository signs of GPE. This impact could likewise be communicated utilizing ordinary electrochemical information. Fig. 2 demonstrates the impact of the glue synthesis on the pinnacle potential division (DEp) and pinnacle current (Ip) of clear GPE in 10 mM K3Fe(CN)6 : K4Fe(CN)6, amongst _0.6 and 1.0 V at a sweep rate of 100 mV s_1. Graphene glue cathodes containing 7, 9, 12, 15, 17, 20, 22, 24 and 26% Nujol oil were utilized.

Immobilization time of probe DNA on the Chit/PB/GPE and the effect of EDC


The affectability of the DNA hybridization test was specifically identified with the surface scope of DNA tests on the terminal, the conduct of DNA hybridization can be influenced by daunomycin. At room temperature, the differential pulse voltammetry (DPV) reactions of the cathode for DNA expanded with an expansion in the immobilization time of the test DNA in Chit film on the PB changed graphene paste terminal and afterward tended to achieve steady values after 10 h.

The impact of PB on the reaction of the altered anode was researched by contrasting the DPV reaction of DNA/Chit/GPE and DNA/Chit/PB/GPE (Fig. 5). From Fig. 5, the DPV reaction of DNA/Chit/GPE (bend an) is appeared to be fundamentally littler than that of DNA/Chit/PB/GPE (bend b) when both terminals are hybridized in 2.12 *10-8 M cDNA arrangement and 1*10-5 M daunomycin. The outcomes affirmed that the utilization of PB can enhance the execution of the changed terminal. This perhaps added to the synergism of PB and graphene in the paste. Furthermore, the capability of DNA/Chit/GPE (bend a) was more positive than that of DNA/Chit/PB/GPE (bend b), the reason might be that PB, as an electrochemical inorganic arbiter, brings about an abatement of the connected potential and the resulting shirking of numerous electrochemical obstructions.

The expository execution of the DNA biosensor was confirmed by utilizing the immobilized test to hybridize the diverse centralizations of the integral grouping as per the depicted strategy. The DPV reaction of the ssDNA/Chit/PB/GPE expanded with an expansion in the centralization of integral target DNA (Fig. 6). The pinnacle streams of the ssDNA/Chit/PB/GPE are straight with the logarithmic estimation of the cDNA succession fixation from 2.12 * 10-8 to 2.12 * 10-11 M.












Detection of cancer cells using a peptide nanotube–folic acid modified graphene electrode


The arrangement of a graphene terminal changed with another conjugate of peptide nanotubes and folic corrosive for the specific discovery of human cervical growth cells over-communicating folate receptors. The functionalization of peptide nanotubes with folic corrosive was affirmed by fluorescence microscopy and nuclear compel microscopy. The peptide nanotube–folic corrosive altered graphene cathode was described by filtering electron microscopy and cyclic voltammetry. The adjustment of the graphene anode with peptide nanotube–folic corrosive prompted an expansion in the ebb and flow flag. The human cervical disease cells were bound to the adjusted cathode through the folic acid–folate receptor cooperation. Cyclic voltammograms within the sight of [Fe(CN)6]3-/4-as a redox animal varieties exhibited that the official of the folate receptor from human cervical disease cells to the peptide nanotube–folic corrosive adjusted cathode brought down the electron move bringing about a decline in the deliberate ebb and flow. A location point of confinement of 250 human cervical malignancy cells per mL was gotten. Control tests affirmed that the peptide nanotube–folic corrosive terminal particularly perceived folate receptors. The altered terminal depicted here opens up new conceivable outcomes for future applications in early stage determinations of sicknesses where cells over-express folate receptors, for example, in growth or leishmaniasis infection.

Experimental section

Synthesis of peptide nanotubes

Stock solution of PNTs was prepared by dissolving the FF peptide powder in the alcohol, 1,1,1,3,3,3-hexafluoro-2-propanol (HFP), at a concentration of 100mgmL-1. The stock solution was further diluted in water to a final concentration of 2 mg mL-1 resulting in the immediate formation of PNTs.

Functionalization of peptide nanotubes with folic acid

FA was dissolved in water with an addition of 50 mL of NaOH (1 M) due to the poor solubility of FA. The FA powder (0.029 g) was mixed with H2O (25 mL) and magnetically stirred until the yellow color became clear. FA was then added to a solution of EDC and stirred for 2 minutes after which 266 mL of FA was added to 1 mL of PNT solution and incubated for 3 hours. The conjugate was washed several times with Milli-Q water and centrifuged to eliminate excess free FA. Fluorescence microscopy and AFM were performed to verify the functionalization of the PNTs with FA. The conjugate was refrigerated at 4 0C awaiting the electrochemical measurements.


Preparation of the modified graphene electrode

A 5 mL drop of a solution containing PNT–FA was deposited on top of the graphene working electrode and incubated for 3 hours at room temperature. The modified electrodes were washed with Milli-Q water prior to the electrochemical measurements to remove any unbound PNTs. The electrodes were then characterized by SEM. The modification steps are shown in Scheme 1.

Cyclic voltammetry measurements

For the CV experiments, the electrodes were immersed in a 10 mM solution of K3[Fe(CN)6] containing 100 mM KCl. All CV measurements were performed at 100 mV s-1 using a screen printed Ag/AgCl as the reference electrode. For the detection of FRs, a solution (40 nM) was used and a CV was measured.

Results and discussion

The conjugate was prepared by a reaction of FA with PNTs in the presence of EDC, which is a commonly used carbodiimide for conjugating biological substances containing carboxylates and amines.38 It was employed as a linker agent to mediate the formation of an amide between the carboxyl group of the FA and the amine group of the PNTs.

An AFM characterization was performed as further evidence of the FA attaching to the PNTs. The scanning area of the

Sample was 2.5 *2.5 mm.


Characterization of the modified electrodes


The CVs of bare and modified graphene electrodes in a 10 mM K3[Fe(CN)6] solution are shown in Fig. 4. Graphene properties and potential uses in the development of electrochemical biosensors have been extensively described. The combination of graphene and PNTs has been found to increase the surface area of a transducer, which was reflected in the current values obtained with the functionalized electrode; its peak current was approximately 28.8% higher than the corresponding value of the bare graphene electrode, Fig. 4.


Detection of folate receptors

FR solution (40 nM) was added and a cyclic voltammogram was measured. Fig. 5 shows a decrease in the peak current of about 18.4%, i.e., from 0.343 to 0.280 mA, after the addition of the FR solution. The electron transfer was reduced when the FRs came closer to the electrode surface containing PNT–FA. Due to the formation of a complex between FA and the FRs, a further barrier was created which hampered the electrochemical process. A calibration curve was prepared by relating the increase in the concentration of FRs with the decrease in the peak current. Using the developed sensor it was possible to detect a FR concentration as low as 8 nM.




An examination of execution of three unique sorts of graphene biosensors for the discovery of prostate particular antigen was accounted for. Three diverse graphene structures were combined by mechanical peeling, microfluidic and self-gathering separately, speaking to graphene composites from immaculate to half and half. Different parameters of various sorts of graphene biosensors were thought about, for example, discovery limits, affectability, security, and so forth. Hybridized materials in the graphene composites will change the electrical solidness. Be that as it may, cross breed or finished materials improve the ingestion of target particle, which present considerably higher affectability and recognition limits. As were normal, self-collected graphene biosensor exhibited the most noteworthy recognition cutoff points and affectability, however demonstrated poor solidness. Then again, immaculate graphene and microfluidic actuated graphene exhibited bring down discovery cutoff points and affectability, yet better soundness because of the nonattendance of half and half polymer in the graphene composites. The outcomes and discourse exhibited here can give a direction to the plan of graphene based biosensors.


Desigining systems of the three sorts of PSA biosensors were outlined in Figure 1. To create unadulterated graphene biosensor, a photoresist layer (Shipley S1818) was utilized as an exchange stamp to shed graphene designs from profoundly situated pyrolytic graphite (HOPG, MikroMasch Inc., ZYA review), and exchanged examples onto a SiO2/Si substrate. From that point onward, chromium/gold layers 50/200 nm thick were kept on the substrate by an AJA sputter framework (Model ATC 2000), and designed to anodes. To create amassed graphene composites without other material cross breed, microfluidic technique was acquainted with store the graphene Nano platelets. Prepatterned substrate was inundated into HF support arrangement (10:1) to get the microchannel 250 nm somewhere down in the silicon dioxide layer. Graphene suspension arrangement were brought into the supply. Because of the hydrophilic property of silicon dioxide, the capillarity instigated the graphene suspension arrangement into the microchannel. Next, the anodes were created as portrayed some time recently. To create hybridized graphene composites, different graphene/PDDA Nano composite layers were layer-by-layer self-gathered on a spotless silicon wafer with SiO2 300 nm thick by drenching the substrate into the accused suspensions of an arrangement of [PDDA (10 min) + PSS (10 min)]2 + [PDDA (10 min) + graphene suspension (20 min)]5. Next, the cathodes were manufactured as portrayed some time recently. After make, the biosensor was functionalized by immobilization of catch immune response at first glance. A graphene sensor was first inundated into a 0.1% poly-l-lysine (PLL) watery arrangement positive charged for 60 minutes. Next, the graphene sensor was brooded for overnight at 4 ºC in PSA catch immune response arrangement at a grouping of 10 μg/ml. Next, the sensor was hatched in 3% BSA blocking arrangement at room temperature for 5 hours to square nonspecific restricting locales. In the wake of rehashing the flushing step, the mark free sensor was prepared for testing. The recognition standards of the graphene biosensor are exhibited in Figure 2. Given that the conductance of graphene is relative to the result of charge transporter thickness and portability, changes in thickness and additionally versatility of charge bearers must be responsive when particles or particles are consumed by graphene. The conductance of the graphene based biosensor altered with the PSA catch counter acting agent moves as the fixation change of PSA arrangements.



After immobilization of PSA catch antibody, the discovery furthest reaches of three sorts of graphene biosensors were portrayed by measuring resistance with substitute distinctive groupings of PSA arrangements arranged by PBS. As is appeared in Figure 3a and 3d, the resistance of unadulterated graphene based biosensor diminished with the expanding of PSA focus from 40 pg/ml to 4 ng/ml. In examination, resistance-versus-time estimations recorded for the other two sorts of graphene biosensors produced and tried under similar conditions. As is appeared in Figure 3b and 3e, microfluidic actuated graphene biosensors were fit for identifying the movements from 4 pg/ml to 4 ng/ml. Also, self-gathered cross breed graphene biosensors had the best location limits from the “progression” reaction of constant estimations. As is appeared in Figure 3c and 3f, the gadget displayed reaction down to 4 fg/ml PSA arrangements. Despite the fact that the self-gathered graphene biosensors demonstrate the most elevated commotion level, the surface profile of this kind of graphene composites have incredible permeable geology, which is more reasonable to enhance catch proteins, giving the best detecting surface range per unit volume. This component adds to as far as possible more. Then again, the immaculate graphene biosensors have the smoothest surface, which shows the most minimal discovery limits.















As the building square of carbon materials of all measurements, graphene shows particular electronic structure, properties, and physicochemistry. Graphene has demonstrated incredible execution in direct electrochemistry of chemical, electrochemical recognition of little biomolecules as a contender to carbon nanotubes, graphene has shown predominant execution in these applications. Notwithstanding, the improvement of graphene-based materials/gadgets is still in its beginnings.

These graphene based biosensors and gadgets have shown great affectability and selectivity towards the location of glucose, cholesterol, Hb, H2O2, little biomolecules, DNA, overwhelming metal particles and, harmful vaporous atoms. Floic receptors biosensor could identify human cervical tumor cells.

Novel techniques for very much controlled synthesis and handling of graphene ought to be created. As expressed in the Introduction, graphene has been integrated with different systems. In any case, the prudent creation approach with high return is as yet not broadly accessible. For electrochemical applications, the approach with chemical/thermal reduction of graphene oxide looks encouraging. Graphene sheets from synthetic/thermal reduction of graphene oxide generally keep an eye on re-stack amid the blend and the preparing .So far, numerous techniques have been proposed in the union and handling of graphene to anticipate re-stacking and to enhance the scattering of graphene in solvents. In a few reports, graphene was created through the electrochemical diminishment of graphene oxide and the electrochemically reduced graphene oxide display much preferred execution for electrochemical applications over synthetically decreased one, which shows a promising methodology in graphene combination and preparing.

Doping graphene with heteroatoms (nitrogen, boron, and so forth.) ought to be researched. Heteroatom doping in carbon nanotubes has appeared to extraordinarily enhance the electro reactant movement.

Better comprehension of material science and science at the surface of graphene and cooperation of chemicals and bimolecules at the interface of graphene will assume an imperative part in applying graphene as nanoscaffold in catalysis, compound/biosensing, imaging and medication conveyance.

In outline, graphene is a brilliant terminal material for electro examination and electro catalysis, and there is still much space for the logical research and application advancement of graphene-based hypothesis, materials, and gadgets.



















1. Ramendra Sundar Dey and C. Retna Raj*

Department of Chemistry, Indian Institute of Technology, Kharagpur J. Phys. Chem. C 2010, 114, 21427–21433.

2. Yinxi Huang,†a Xiaochen Dong,†b Yuxin Liu,a Lain-Jong Lic and Peng Chen*a J. Mater. Chem., 2011, 21, 12358.

3. Numan Celik ✉, Wamadeva Balachandran, Nadarajah Manivannan IET Circuits Devices Syst., 2015, Vol. 9.



6. Yang Bo, Weiqi Wang, Junfei Qi and Shasheng Huang* DOI: 10.1039/c1an15084g.

7. John J. Castillo,ab Winnie E. Svendsen,b Noemi Rozlosnik,b Patricia Escobar,c

Fernando Mart´ıneza and Jaime Castillo-Le´on*b DOI: 10.1039/c2an36121c


17th International Conference on Miniaturized Systems for Chemistry and Life Sciences 27-31 October 2013, Freiburg, Germany

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