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Enzymes, biosensors enhancers

The first enzyme biosensor was a glucose sensor reported by Clark in 1962 [194], This biosensor measured the product of glucose oxidation by GOD using an electrode which was a remarkable achievement even though the enzyme was not immobilized on the electrode. Updark and Hicks have developed an improved enzyme sensor using enzyme immobilization [194], The sensor combined the membrane-immobilized GOD with an oxygen electrode, and oxygen measurements were carried out before and after the enzyme reaction. Their report showed the importance of biomaterial immobilization to enhance the stability of a biosensor. [Pg.573]

Figure 18 Schematic of a glucose biosensor assembled from diphenylalanine peptide nanotubes. The enzyme GOX has been cross-linked to these nanotubes, which are further linked to the gold (Au) electrode and immobilized in a polyethyleneimine (PEI) matrix. The nanofibers act in two ways they immobilize the sensing enzyme and enhance the transducer. Reprinted in part with permission from Yemini et al. (2005a) (copyright 2005 American Chemical Society). Figure 18 Schematic of a glucose biosensor assembled from diphenylalanine peptide nanotubes. The enzyme GOX has been cross-linked to these nanotubes, which are further linked to the gold (Au) electrode and immobilized in a polyethyleneimine (PEI) matrix. The nanofibers act in two ways they immobilize the sensing enzyme and enhance the transducer. Reprinted in part with permission from Yemini et al. (2005a) (copyright 2005 American Chemical Society).
The intrinsic conductivity of the ionogels can also be exploited to prepare electrochemical sensors. As an example, IL-modified electrodes for enzymatic electrochemical reaction were prepared by sol-gel. An amperometric biosensor was obtained using ionogel fihn doped with HRP and ferrocene. The ionogel retain the native structure of the enzymes and enhance the electrochemical response at electrode [68]. [Pg.496]

Willner and coworkers have extended this approach to electron relay systems where core-based materials facilitate the electron transfer from redox enzymes in the bulk solution to the electrode.56 Enzymes usually lack direct electrical communication with electrodes due to the fact that the active centers of enzymes are surrounded by a thick insulating protein shell that blocks electron transfer. Metallic NPs act as electron mediators or wires that enhance electrical communication between enzyme and electrode due to their inherent conductive properties.47 Bridging redox enzymes with electrodes by electron relay systems provides enzyme electrode hybrid systems that have bioelectronic applications, such as biosensors and biofuel cell elements.57... [Pg.321]

Perhaps the original hope for these polymers was that they would act simultaneously as immobilisation matrix and mediator, facilitating electron transfer between the enzyme and electrode and eliminating the need for either O2 or an additional redox mediator. This did not appear to be the case for polypyrrole, and in fact while a copolymer of pyrrole and a ferrocene modified pyrrole did achieve the mediation (43), the response suggested that far from enhancing the charge transport, the polypyrrole acted as an inert diffusion barrier. Since these early reports, other mediator doped polypyrroles have been reported (44t45) and curiosity about the actual role of polypyrrole or any other electrochemically deposited polymer, has lead to many studies more concerned with the kinetics of the enzyme linked reactions and the film transport properties, than with the achievement of a real biosensor. [Pg.17]

The hydrophobias are a case where protein nanofibers can play a dual role in creating a biosensor. They can aid in the immobilization of bioactive components within a biosensor and also add further functionality to the transducing element of a biosensor device. Hydrophobins are self-assembling [3-sheet structures observed on the hyphae of filamentous fungi. They are surface active and aid the adhesion of hyphae to hydrophobic surfaces (Corvis et al., 2005). These properties can be used to create hydrophobia layers on glass electrodes. These layers can then facilitate the adsorption of two model enzymes glucose oxidase (GOX) and hydrogen peroxidase (HRP) to the electrode surface. The hydrophobin layer also enhances the electrochemical properties of the electrodes. [Pg.194]

Fig. 23. Schematic design of a biosensor that can be mounted in situ. The biosensor itself sits in a housing and consists of a biocomponent such as one or more immobilized enzymes or cells on top of and in close contact with a suitable type of transducer. A buffer or diluent stream can help to extend the useful dynamic range of the biosensor. The analyte arrives at the biosensor by passing a suitable membrane which enhances selectivity and protects the biosensor. An additional mechanical shield in the form of a mesh, grid or frit may be necessary to assure mechanical stability in the highly turbulent zone... Fig. 23. Schematic design of a biosensor that can be mounted in situ. The biosensor itself sits in a housing and consists of a biocomponent such as one or more immobilized enzymes or cells on top of and in close contact with a suitable type of transducer. A buffer or diluent stream can help to extend the useful dynamic range of the biosensor. The analyte arrives at the biosensor by passing a suitable membrane which enhances selectivity and protects the biosensor. An additional mechanical shield in the form of a mesh, grid or frit may be necessary to assure mechanical stability in the highly turbulent zone...

See other pages where Enzymes, biosensors enhancers is mentioned: [Pg.358]    [Pg.2523]    [Pg.54]    [Pg.1379]    [Pg.197]    [Pg.412]    [Pg.11]    [Pg.208]    [Pg.573]    [Pg.278]    [Pg.108]    [Pg.256]    [Pg.10]    [Pg.449]    [Pg.451]    [Pg.450]    [Pg.272]    [Pg.488]    [Pg.489]    [Pg.496]    [Pg.538]    [Pg.540]    [Pg.564]    [Pg.568]    [Pg.592]    [Pg.270]    [Pg.148]    [Pg.289]    [Pg.395]    [Pg.644]    [Pg.137]    [Pg.644]    [Pg.108]    [Pg.270]    [Pg.314]    [Pg.17]    [Pg.194]    [Pg.273]    [Pg.190]    [Pg.871]    [Pg.291]    [Pg.133]   
See also in sourсe #XX -- [ Pg.75 ]




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