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
Flow-injection determination of glucose in serum with an immobilized pyranose oxidase reactor
β Scribed by Nobutoshi Kiba; Fumito Ueda; Motohisa Furusawa; Takeshi Yamane
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 386 KB
- Volume
- 269
- Category
- Article
- ISSN
- 0003-2670
No coin nor oath required. For personal study only.
β¦ Synopsis
A flow-mqectlon system for the chemdummometnc determmatlon of o-glucose m serum with an lmmobdlzed pyranose oxldase reactor IS described Pyranose oxldase IS lmmobdlzed on controlled-pore glass beads and packed mto a stamless-steel column Serum (100 nl) IS dduted lOWfold with water Sample solution (10 ~1) IS Injected mto the tamer stream The hydrogen peroxrde produced IS detected by measurmg the chemdummescence emltted on adrmxmg with lummol and potassmm hexacyanoferrate(II1) The maximum sample throughput IS 60 h-' The cahbratlon graph 1s linear from 0 2 to 500 PM glucose, the detectlon hmlt IS 0 05 PM The lmmobdlzed enzyme reactor IS stable for at least 2 months
π SIMILAR VOLUMES
A spectrophotometric, continuous flow-injection, merging zones manifold including an enzyme reactor was used for the determination of magnesium ion in serum by exploiting the activating effect of MgfII) on the hydrolysis of o-nitrophenyl-B-o-galactopyranoside by j?-o-galactosidase immobiliied on con
A flow-injection system for the determination of 3-hydroxybutyrate in serum is described. 3-Hydroxybutyrate dehydrogenase is immobilized on poly(vinyl alcohol) beads and incorporated in a flow-injection system. 1-Methoxy-Smethylphenazinium methylsulphate reacts with enzymatically generated NADH to g
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