Modification of thermally expanded graphite and its effect on the properties of the amperometric biosensor.
Yulia V PlekhanovaSergey E TarasovAnna KitovaVladimir KolesovVadim KashinAshok K SundramoorthyAnatoly N ReshetilovPublished in: 3 Biotech (2022)
The work considered the properties of a biosensor based on a novel nanomaterial-modified thermally expanded graphite (TEG M ). The main focus was on whether the procedure of additional graphite thermal expansion would affect the electrochemical properties of biosensors based on membrane fractions of acetic acid bacteria Gluconobacter oxydans . Raman spectroscopy, scanning electron microscopy and electrochemical analysis were used for the study. Raman spectra showed that the formation of TEG M led to its stratification into smaller particles and a better orderly layered structure with high "graphenization" degree. Modification of TEG led to the formation of additional cavities into which bacterial cells or bacterial membrane fractions could be immobilized and affect the electrical conductivity of the biosensors positively. Calculation of the heterogeneous charge transfer constants showed that processes occurring on the electrodes are quasi-reversible. The limiting stage of these processes is the transfer of an electron from a biological component on the electrode surface, not the diffusion of the analyte from the solution to the active centers of the enzyme. We showed the possibility of developing third-generation mediator-free biosensors for glucose detection based on TEG M , as well as of second-generation mediator biosensors for glucose, ethanol and glycerol detection.
Keyphrases
- label free
- electron microscopy
- raman spectroscopy
- reduced graphene oxide
- light emitting
- solid state
- induced apoptosis
- blood glucose
- gold nanoparticles
- cell cycle arrest
- blood pressure
- signaling pathway
- carbon nanotubes
- oxidative stress
- hydrogen peroxide
- adipose tissue
- metabolic syndrome
- density functional theory
- molecular dynamics
- weight loss
- cell death
- loop mediated isothermal amplification
- real time pcr