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Biomedical subjects

G F Khan

Publications and source records attributed to G F Khan.

3 recordsLinked to original sources

Design of a stable charge transfer complex electrode for a third-generation amperometric glucose sensor.

A novel approach to prepare a stable charge transfer complex (CTC) electrode for the direct oxidation of flavoproteins and the fabrication of a third generation amperometric biosensor (Koopal, C.G.J.; Feiters, M.C.; Nolte, R.J.M. Bioelectrochem. Bioenerg. 1992, 29, 159-175) system is described. Tetrathiafulvalene-tetracyanoquinodimethane (TTF-TCNQ), an organic CTC, is grown at the surface of a shapable electroconductive (SEC) film (a polyanion-doped polypyrrole film) in such a way that it makes a tree-shaped crystal structure standing vertically on the surface. Glucose oxidase (GOx) is adsorbed and cross-linked with glutaraldehyde to fix at the surface of the CTC structure. The space between crystals is filled with cross-linked gelatin to ensure the stability of the treelike crystal structure as well as the stability of the enzyme. Because of the close proximity and the favorable orientation of the enzyme at the CTC surface, the enzyme is directly oxidized at the crystal surface, which leads to a glucose sensor with remarkably improved performance. It works at a potential from 0.0 to 0.25 V (vs Ag/AgCl). The maximum current density at 0.25 V reaches 1.8 mA/cm2, with an extended linear range. The oxygen in the normal buffer solution has little effect on the sensor output. The current caused by interference contained in the physiological fluids is negligible. The working life as well as the shelf life of the sensor is substantially prolonged. The sensor was continuously used in a flow injection system with a continuous polarization at 0.1 V, and the samples (usually 10 mM glucose) were injected at 30 min intervals. After 100 days of continuous use, the current output dropped to 40% of the initial level. No change in the output of the sensor was observed over a year when the sensor was stored dry in a freezer. The electrochemical rate constants and the effective Michaelis constant of the system are reported.

Biosensing Techniques

Organic charge transfer complex based printable biosensor.

This paper describes the preparation of an organic charge transfer complex (CTC) based printable enzyme electrode. CTC crystals were prepared by mixing TCNQ powder with TTF solution (in acetonitrile). Glucose oxidase (GOD) was adsorbed at the CTC crystal surface in a monolayer. A printable paste was prepared by mixing GOD-absorbed crystals with a binder and a solvent. This paste was applied to an electrode cavity and vacuum dried. A thin layer of gelatin was cast on the paste filled dried electrode, and cross-linked with glutaraldehyde in the dry condition. The sensors were fixed in a flow injection system, and continuously polarized at 0.15 V and 37 degrees C, and the samples were automatically injected every 30 min. The developed sensors produced a huge response current with an extended linear range of detection (0-100 mM) and the response was unaffected by the presence of normal oxygen in the buffer solution. The sensor showed excellent stability. The performance of the sensors was significantly influenced by the binder used.

Biosensing Techniques

Electronically modulated biological functions of molecular interfaced enzymes and living cells.

Conducting polymer molecular interfaces have been implemented to modulate biological functions of fructose dehydrogenase, pyruvate oxidase and Saccharomyces cerevisiae at the electrode surface by adjustment of electrode potential. The enzyme activity of the polypyrrole-interfaced fructose dehydrogenase was electronically modulated by means of electron transfer between the enzyme and the electrode surface. The enzyme activity of polypyrrole-interfaced pyruvate oxidase was modulated by an electronically driven change of substrate concentration. The gene expression in polypyrrole-interfaced Saccharomyces cerevisiae was electronically induced by a change in the phosphate concentration.

Electrodes