Kahlouche et al. [41] showed that electrophoretic deposition of reduced graphene oxide
and polyethyleneimine can be used to selectively modify a gold (Au) microelectrode in a
microsystem with a Pt counter and an Ag/AgCl reference electrode. With a detection
limit of 50 nM, the functionalized microsystem was effectively used to detect dopamine.
The microsystem was employed to detect dopamine levels in meat (beef and chicken)
samples. Akkaya et al. [42] proposed a biosensor based on direct electrochemistry of
glucose oxidase on a tannic acid–reduced graphene oxide nanocomposite modified glassy
carbon electrode coated with Pt nanoparticles. Tannic acid was used to provide a
switchable surface with changes in both pH and temperature. It also helps for green
reduction of Pt4+ and graphene oxide and then altering the reduced GO for GOx im
mobilization. The redox peaks were found at a formal potential of 0.462 V with a peak
separation (Ep) of 56 mV which indicates that there is a quick electron transport. The
glucose oxidation response was linear and was in the range of 210 mM with a sensitivity
of 27.51 A mM‒1cm2, and the detection limit was 1.21 mM. The development of the
shrunken and compact globule poly(N-isopropyl acrylamide) structure and variable
surface charge resulted in the fabrication of an on-off biosensor with zipperlike interfacial
properties after the deposition of poly(N-isopropyl acrylamide) onto the created bio
sensor via hydrogen bonding. The cyclic voltammetric response of the developed bio
sensor is shown in Figure 16.6.
Due to the signal transduction mechanism and unique working principles of functio
nalized graphene field-effect transistors (gFETs), functionalized graphene field-effect
transistors (gFETs) have recently exhibited astonishingly low detection limits for trace
biomarkers using crumpled graphene channels, which greatly increase gFET device
performance for sensitive nucleic acid detection. The authors create wrinkled gFET
channels using both substrate deformation and no substrate distortion. DNA is im
mobilized on the graphene channel via a pyrenebutanoic acid succinimidyl ester linker,
and the target DNA is hybridized with a probe strand of DNA to allow for selective
detection. Wu et al. [43], for example, developed dual-aptamer modified gFET biosensors
for label-free detection of HCC-derived microvesicles in clinical blood samples. For the
collection and measurement of these microvesicles, 62 gold nanoparticles containing both
HCC-derived microvesicles cell-specific TLS11a aptamer and epithelial cell adhesion
molecule aptamer (AptEpCAM) were attached to the gFET channel. Using their gFET
biosensing platforms, the scientists discovered substantial differences in microvesicles’
amounts between healthy control groups and HCC patients, indicating a promising po
tential for early HCC detection.
Lian et al. [44] developed a novel piezoelectric sensor for quick and selective detection
of Staphylococcus aureus with an aptamer/graphene interdigitated gold electrode.
4-mercaptobenzene-diazonium tetrafluoroborate salt was used for molecular cross-
linking to bind graphene with the gold electrodes which is coupled to piezoelectric quartz
crystal electrodes. When Staphylococcus aureus was put onto the surface of graphene, the
detection signal was recorded in the oscillator frequency of the quartz crystal (piezo
electric) electrodes. The good electronic conductivity provided by graphene resulted in a
variation in the electric properties of the prepared electrode. The graphene-based na
nostructures have been used for the recording of electrical activity both in vivo and in
vitro. The greatest branded two-dimensional graphene electrode assemblies comprised
of graphene as a passive electrode, such as electrode material in multi-electrode
arrays or used as an active electrode, such as a semiconducting channel in field-effect
transistors. Furthermore, the mechanical properties of graphene enable the development
of bioelectronics on both rigid and flexible surfaces. The high transparency of this
Graphene Nanostructures
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