A flow injection analysis method for determining L-carnitine is reported. The system uses the enzyme L-carnitine dehydrogenase covalently immobilized to Eupergit C. The NADH produced by the action of the enzyme, which is proportional to the L-carnitine concentration, is quantified using fluorescence
Chemiluminometric l-lysine determination with immobilized lysine oxidase by flow-injection analysis
β Scribed by F. Preuschoff; U. Spohn; E. Weber; K. Unverhau; K.-H. Mohr
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 407 KB
- Volume
- 280
- Category
- Article
- ISSN
- 0003-2670
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β¦ Synopsis
An enzymatic flow-injection procedure for the determination of L-lysine was developed. A lysine oxidase reactor is combined with a fibre-optic hydrogen peroxide detector. Hydrogen peroxide detection is based on the peroxidasecatalysed luminol reaction. The chemiluminescent light is detected by a photomultiplier. L-Lysine can be determined in the range 10-1000 PM. A sampling rate of up to 90 b-' can be achieved. The whole sensing assay works for more than 1 month. The double logarithmic graph of the peak signal height vs. the lysine concentration is linear, the slope being larger than unity (r* = 0.991, n = 4).
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L-Glutamate oxldase was unmoblhzed on Ammo-Cellulofine and used as an enzyme reactor III a flow-mjectlon system The hydrogen peroxrde produced was momtored amperometncally A new configurabon IS described for the detenmnatlon of L-glutamate m food samples for which the matnx provides varymg blank val
A flow-injection system with a co-immobilized enzyme reactor is described for the determination of 3-hydroxybutyrate. 3-Hydroxybutyrate dehydrogenase and NADH oxidase were immobilized on aminated poly (vinyl alcohol) beads and packed into a stainless-steel column (5 cm X 4 mm i.d.). Serum was dilute
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