Title of article
A fully automated method for the determination of starch in foodstuff was developed. The method is based on the standard procedure involving leaching of sugars from the sample, hydrolysis of the analyte, and colorimetric determination of the hydrolysis pr
Author/Authors
Robert Koncki، نويسنده , , Izabela Wa?cerz، نويسنده , , Falk Ruckruh، نويسنده , , Stanis?aw G?ab، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 1996
Pages
8
From page
215
To page
222
Abstract
Ammonium-selective electrodes enzymatically sensitized for creatine and l-arginine are presented. Enzyme layers of these biosensors contain two enzymes: urease and, as a second enzyme, creatinase or arginase dependent on the analyte (substrate): creatine or arginine. The bienzymatic layer with such a composition sequentially converts the analyte into ammonium ions, which are detectable by the internal sensor. Monomolecular and bimolecular bienzymatic layers immobilized directly on the ammonium sensitive membrane were used. The covalent binding of enzymes to the matrix of the ion-selective membrane made of the carboxylated poly(vinyl chloride) was performed using carbodiimide and glutaraldehyde. The extremely thin enzyme layers are strongly bound and easily penetrable. Therefore the presented biosensors are stable and respond rapidly, t95% varies from 1.5 to 4 min. The linear ranges of both biosensors were 0.1–30 mM and the detection limits were below 10−5 M.
Keywords
Biosensors , Potentiometry , Bienzyme electrode , Enzyme immobilization , l-arginine , Creatine
Journal title
Analytica Chimica Acta
Serial Year
1996
Journal title
Analytica Chimica Acta
Record number
1025147
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