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A stable three-enzyme creatinine biosensor. 3. Immobilization of creatinine amidohydrolase and sensor development

โœ Scribed by Jason A. Berberich; Andy Chan; Mark Boden; Alan J. Russell


Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
144 KB
Volume
1
Category
Article
ISSN
1742-7061

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โœฆ Synopsis


We describe the development of an extended use amperometric three-enzyme creatinine biosensor and the successful chemical modification and immobilization of the enzyme creatinine amidohydrolase using polyurethane prepolymers. Creatinine amidohydrolase is significantly stabilized by immobilization in polyurethane polymers. The half-life increases from six to more than 80 days in buffer at 37 ยฐC. The effect of silver ions leached from amperometric reference electrodes on enzyme and sensor performance is discussed. The use of cellulose acetate cover membranes to prevent silver from reaching the enzyme is investigated. Sensors prepared with cover membranes have half-lives almost an order of magnitude greater than those prepared with no cover membrane over the silver electrode. The complete biosensor has been constructed on a clinical blood analyzer platform and is stable for many days.


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A stable three-enzyme creatinine biosens
โœ Jason A. Berberich; Lee Wei Yang; Jeff Madura; Ivet Bahar; Alan J. Russell ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 172 KB

The determination of creatinine levels in biological fluids is an increasingly important clinical requirement. Amperometric biosensors have been developed based on a three-enzyme system which converts creatinine to amperometrically measurable hydrogen peroxide. The development of the amperometric cr