During the continuing rapid daelopment of analytical methods based on immobilized enzymes, several techniques have been described for the determination of glucose. For example, glucose oxidase (E.C.1.1.3.4) entrapped in polyacrylamide gel was used by Updike and Hicks in two methods. In one case [l]
Flow injection amperometric and chemiluminescence individual and simultaneous determination of lysine and glucose with immobilized lysine oxidase and glucose oxidase
β Scribed by Ala'ddin M. Almuaibed; Alan Townshend
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- English
- Weight
- 555 KB
- Volume
- 338
- Category
- Article
- ISSN
- 0003-2670
No coin nor oath required. For personal study only.
β¦ Synopsis
Flow injection amperometric and chemiluminescence methods for the individual and simultaneous determination of lysine and glucose by using lysine oxidase and glucose oxidase are described in this paper. The calibration graphs for lysine are linear over the range 1 x lOA -1.6x lO-4 and 2.05 x 10W7-2.75 x 10m5 M for amperometric and chemiluminescence detection, respectively. The detection limits (3a) for lysine are 5 x lop6 M with amperometric and 4.0 x 10m8 M with chemiluminescence detection. The sample throughput rates are 80 and 100 h-l, respectively. Lysine and glucose concentrations can be monitored simultaneously in the range 1.5-9x lop5 M and 7 x 10d7-8 x lop6 M with amperometric and chemiluminescence detection, respectively. The interference effects of some amino acids and metal ions are examined. An on-line cation-exchange minicolumn is inserted into the chemiluminescence manifold to remove the interference effect of Fe2+ and Cu2+.
π SIMILAR VOLUMES
A flow-injection system with anodic aniperometric detection for glucose determination in human blood serum samples was optimized by a comparison of various arrangements of enzyme immobilization and the elimination o f interferences. The best results were obtained using a compact membrane biosensor i
A flow-mjectlon system wth a separation column and an unmobdlzed enzyme reactor 1s described for the determmatlon of l$anhydro-o-glucitol in serum Serum samples diluted mth water are injected into an amon-exchange column (4 cm x 4 mm I d ) The eluate 1s passed through an unmobdlzed pyranose oxldase