Development of Enzyme Biosensor Based on ISFETs for Quantitative Analysis of Serine Proteinases

A new potentiometric biosensor allowing quantitative determination of the proteinases through their esterase activity has been developed. The biosensor, specific for ester artificial substrates of serine proteinases has been fabricated using a pH‐sensitive field effect transistor (pH‐FET) and an imm...

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Published inElectroanalysis (New York, N.Y.) Vol. 16; no. 22; pp. 1883 - 1889
Main Authors Biloivan, Olga A., Dzyadevych, Sergiy V., Boubriak, Olga A., Soldatkin, Alexey P., El'skaya, Anna V.
Format Journal Article
LanguageEnglish
Published Weinheim WILEY-VCH Verlag 01.11.2004
WILEY‐VCH Verlag
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Summary:A new potentiometric biosensor allowing quantitative determination of the proteinases through their esterase activity has been developed. The biosensor, specific for ester artificial substrates of serine proteinases has been fabricated using a pH‐sensitive field effect transistor (pH‐FET) and an immobilized complex of trypsin and α2‐macroglobulin. It has been shown that created biosensor is able to determine the activity of the soluble trypsin in the range of 0.1–30 U/mL (substrate BAEE). The relative standard deviation for the trypsin determination was approximately 3%. The operation stability of the biosensor was no less than 12 h (40 measurements). The response of the biosensor stored at +4 °C was stable for 30 days.
Bibliography:ark:/67375/WNG-43QKK3C6-2
istex:F1BDB1051F3118355325CD014C82D0D912A36138
ArticleID:ELAN200403076
ISSN:1040-0397
1521-4109
DOI:10.1002/elan.200403076