Graphene has emerged as a champion material for a variety of applications cutting across multiple disciplines in science and engineering. Graphene and its derivatives have displayed huge potential as a biosensing material due to their unique physicochemical properties, good electrical conductivity, optical properties, biocompatibility, ease of functionalization, and flexibility. Their widespread use in making biosensors has opened up new possibilities for early diagnosis of life-threatening diseases and real-time health monitoring. Following an introduction and discussion on the significance of fabrication protocols and assembly, this review is intended to assess why graphene is suitable to build better biosensors, the working of existing biosensing schemes and their current status toward commercialization for wearable diagnostic and prognostic devices. We believe this review will provide a critical insight for harnessing graphene as a suitable biosensor for the clinical diagnostics, its future prospects and challenges ahead.
We present a net-shaped DNA nanostructure (called “DNA Net” herein) design strategy for selective recognition and high-affinity capture of intact SARS-CoV-2 virions through spatial pattern-matching and multivalent interactions between the aptamers (targeting wild-type spike-RBD) positioned on the DNA Net and the trimeric spike glycoproteins displayed on the viral outer surface. Carrying a designer nanoswitch, the DNA Net-aptamers release fluorescence signals upon virus binding that are easily read with a handheld fluorimeter for a rapid (in 10 min), simple (mix-and-read), sensitive (PCR equivalent), room temperature compatible, and inexpensive (∼$1.26/test) COVID-19 test assay. The DNA Net-aptamers also impede authentic wild-type SARS-CoV-2 infection in cell culture with a near 1 × 10 3 -fold enhancement of the monomeric aptamer. Furthermore, our DNA Net design principle and strategy can be customized to tackle other life-threatening and economically influential viruses like influenza and HIV, whose surfaces carry class-I viral envelope glycoproteins like the SARS-CoV-2 spikes in trimeric forms.
Graphene, a two-dimensional nanomaterial, has gained immense interest in biosensing applications due to its large surface-to-volume ratio, and excellent electrical properties. Herein, a compact and user-friendly graphene field effect transistor (GraFET) based ultrasensitive biosensor has been developed for detecting Japanese Encephalitis Virus (JEV) and Avian Influenza Virus (AIV). The novel sensing platform comprised of carboxy functionalized graphene on Si/SiO 2 substrate for covalent immobilization of monoclonal antibodies of JEV and AIV. The bioconjugation and fabrication process of GraFET was characterized by various biophysical techniques such as Ultraviolet-Visible (UV-Vis), Raman, Fourier-Transform Infrared (FT-IR) spectroscopy, optical microscopy, Scanning Electron Microscopy (SEM) and Atomic Force Microscopy (AFM). The change in the resistance due to antigenantibody interaction was monitored in real time to evaluate the electrical response of the sensors. The sensors were tested in the range of 1 fM to 1 μM for both JEV and AIV antigens, and showed a limit of detection (LOD) upto 1 fM and 10 fM for JEV and AIV respectively under optimised conditions. Along with ease of fabrication, the GraFET devices were highly sensitive, specific, reproducible, and capable of detecting ultralow levels of JEV and AIV antigen. Moreover, these devices can be easily integrated into miniaturized FET-based real-time sensors for the rapid, cost-effective, and early Point of Care (PoC) diagnosis of JEV and AIV. The development of Point of Care (PoC) disease detection kits providing ultra-sensitive, selective, and rapid advances in recent times. In this article, we have focused on graphene-based biosensors for the detection of two different viruses by detecting their respective viral antigen i.e. Japanese encephalitis virus (JEV) and Avian Influenza Virus (AIV). JEV belongs to the family Flaviviridae genus Flavivirus 1 and exists in a zoonotic cycle between the vector i.e. Culex mosquitos, while humans are the dead end host due to low and short-lived viremia of JEV 2-5. Most infections of JEV are asymptomatic, however, the case-fatality rate among those with encephalitis can be as high as 30%, or more in children. It causes clinical symptoms in humans, including a non-specific febrile illness, meningitis, encephalitis and meningo-encephalitis. Pigs play an important role and serve as an amplifier and have a natural infection rate of 98-100% 6. As JEV is incurable and the vaccination is not full-proof, an early diagnosis is critical in preventing an epidemic outbreak, especially since the initial symptoms are usually mistaken for dengue or malaria. The conventional diagnostic methods for JEV 7 such as Enzyme-Linked Immunosorbent Assays (ELISA) 8 ,
Intent of present investigation is to improve the properties of graphite-polymer composite bipolar plate by nanostructuring. This involves the incorporation of different vol.% of multiwall carbon nanotubes (MWNTs) in graphite-polymer composite bipolar plate. It has been found that by inclusion of 1 vol.% of MWNTs in graphite composite plate, the electrical and thermal conductivity of nanocomposite increased by 100%. The thermal conductivity of nanocomposite plate increases from 1 W/m K to 13 W/m K in throughplane and in-plane from 25 W/m K to 50 W/m K at 1 vol.% of MWNTs. This significant enhancement is due to the orientation of MWNTs in all the directions of composite, positive synergistic effect of MWNTs and heat transfer along the axis directions. However, bending strength of nanocomposite increases by 25% and maximum augmentation is in case of 1 vol. % of MWNTs. The improvement in conductivity of nanocomposite plate is due to an increase in the electron transfer ability within the composite plate which influences the I-V performance of ultimate fuel cell. These observations confirm that the optimal content of MWNTs is 1 vol.%, in graphite-polymer composite.
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