Since its discovery in 2004, graphene has enticed engineers and researchers from various fields to explore its possibilities to be incepted into various devices and applications. Graphene is deemed a ‘super’ material by researchers due to its extraordinary strength, extremely high surface-to-mass ratio and superconducting properties. Nonetheless, graphene has yet to find plausible footing as an electronics material. In biomedical field, graphene has proved useful in tissue engineering, drug delivery, cancer teraphy, as a component in power unit for biomedical implants and devices and as a vital component in biosensors. Graphene is used as scaffolding for tissue regeneration in stem cell tissue engineering, as active electrodes in supercapacitor for powering wearable and implantable biomedical devices and as detectors in biosensors. In tissue engineering, the extreme strength of monolayer graphene enables it to hold stem cell tissues as scaffold during in-vitro cell regeneration process. In MEMS supercapacitor, graphene's extremely high surface-to-mass ratio enables it to be used as electrodes in order to increase the power unit's energy and power densities. A small yet having high energy and power densities cell is needed to power often space constrainted biomedical devices. In FET biosensors, graphene acts as detector electrodes, owing to its superconductivity property. Graphene detector electrodes is capable of detecting target molecules at a concentration level as low as 1 pM, making it the most sensitive biosensor available today. Graphene continues to envisage unique and exciting applications for biomedical field, prompting continuous research which results and implementation could benefit the general public in decades to come.
The race towards the development of user-friendly, portable, fast-detection, and low-cost devices for healthcare systems has become the focus of effective screening efforts since the pandemic attack in December 2019, which is known as the coronavirus disease 2019 (COVID-19) pandemic. Currently existing techniques such as RT-PCR, antigen-antibody-based detection, and CT scans are prompt solutions for diagnosing infected patients. However, the limitations of currently available indicators have enticed researchers to search for adjunct or additional solutions for COVID-19 diagnosis. Meanwhile, identifying biomarkers or indicators is necessary for understanding the severity of the disease and aids in developing efficient drugs and vaccines. Therefore, clinical studies on infected patients revealed that infection-mediated clinical biomarkers, especially pro-inflammatory cytokines and acute phase proteins, are highly associated with COVID-19. These biomarkers are undermined or overlooked in the context of diagnosis and prognosis evaluation of infected patients. Hence, this review discusses the potential implementation of these biomarkers for COVID-19 electrical biosensing platforms. The secretion range for each biomarker is reviewed based on clinical studies. Currently available electrical biosensors comprising electrochemical and electronic biosensors associated with these biomarkers are discussed, and insights into the use of infection-mediated clinical biomarkers as prognostic and adjunct diagnostic indicators in developing an electrical-based COVID-19 biosensor are provided.
Nephrogenic diabetes insipidus (NDI), which can be congenital or acquired, results from the failure of the kidney to respond to the anti-diuretic hormone (ADH). This will lead to excessive water loss from the body in the form of urine. The kidney, therefore, has a crucial role in maintaining water balance and it is vital to restore this function in an artificial kidney. Herein, an ultrasensitive and highly selective aptameric graphene-based field-effect transistor (GFET) sensor for ADH detection was developed by directly immobilizing ADH-specific aptamer on a surface-modified suspended graphene channel. This direct immobilization of aptamer on the graphene surface is an attempt to mimic the functionality of collecting tube V 2 receptors in the ADH biosensor. This aptamer was then used as a probe to capture ADH peptide at the sensing area which leads to changes in the concentration of charge carriers in the graphene channel. The biosensor shows a significant increment in the relative change of current ratio from 5.76 to 22.60 with the increase of ADH concentration ranging from 10 ag/mL to 1 pg/mL. The ADH biosensor thus exhibits a sensitivity of 50.00 µA· ( g / mL ) - 1 with a limit of detection as low as 3.55 ag/mL. In specificity analysis, the ADH biosensor demonstrated a higher current value which is 338.64 µA for ADH-spiked in phosphate-buffered saline (PBS) and 557.89 µA for ADH-spiked in human serum in comparison with other biomolecules tested. This experimental evidence shows that the ADH biosensor is ultrasensitive and highly selective towards ADH in PBS buffer and ADH-spiked in human serum.