Biosensors based on carbon paste electrodes using immobilized dehydrogenase enzymes. An overview and trends

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dc.contributor.author Lobo-Castañón, Maria Jesus
dc.contributor.author Alvarez-Crespo, Suzana L.
dc.contributor.author Alvarez-Gonzalez, Maria Isabel
dc.contributor.author Saidman, Silvana B.
dc.contributor.author Miranda-Ordieres, Arturo José
dc.contributor.author Tunon-Blanco, Paulino
dc.date.accessioned 2021-02-22T11:29:04Z
dc.date.available 2021-02-22T11:29:04Z
dc.date.issued 1997
dc.identifier Univerzitní knihovna (studovna) cze
dc.identifier.issn 1211-5541
dc.identifier.uri https://hdl.handle.net/10195/76832
dc.description.abstract Amperometric biosensors based on two different NADH catalytic systems are presented. Common to both types is the design strategy which consists in the direct mixing of the NAD' -dependent dehydrogenase enzymes and other modifying molecules with the carbon paste combined with physical barriers like dialysis membranes or conducting polymers. One type is based on the use of a redox mediator (the phenothiazine dye Toluidine Blue O) to make possible the electrocatalytic oxidation of the enzymatically produced NADH at potentials close to 0 V. The second type is based on the use of the electrochemically generated conducting polymers poly(o-aminophenol) (PAP) and poly(o­phenylenediamine) (PPD), which allow not only the immobilization of enzyme and cofactor at the electrode surface but also the amperometric detection of NADH at potentials as low as 0 V without other immobilized electron transfer mediators. An ethanol biosensor based on the first catalytic system and ethanol, lactate and glutamate sensors based on the second one are presented. cze
dc.format p. 17-29
dc.language.iso en cze
dc.publisher Univerzita Pardubice cze
dc.relation.ispartof Scientific papers of the University of Pardubice. Series A, Faculty of Chemical technology. 3(1997) eng
dc.rights open access eng
dc.title Biosensors based on carbon paste electrodes using immobilized dehydrogenase enzymes. An overview and trends cze
dc.type Article cze
dc.identifier.signature 47333-3
dc.peerreviewed yes eng
dc.publicationstatus published eng


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