A new, Modern, COST-Saving micro/macro method for the determination of serum fructosamine

Author:

Oppel Klára1,Bárdos L.2,Ferencz A.3,Lakner Hajnalka4,Simon Judit5,Temesváry Kriszta6,Karchesz Krisztina7,Kulcsár Margit8

Affiliation:

1. 1 Department of Animal Physiology and Health, Faculty of Agriculture and Environmental Science, Szent István University Please ask the editor of the journal.

2. 2 Department of Animal Physiology and Hygiene, Faculty of Animal Science, University of Kaposvár Please ask the editor of the journal.

3. 3 Department of Animal Physiology and Health, Faculty of Agriculture and Environmental Science, Szent István University Please ask the editor of the journal.

4. 4 Department of Animal Physiology and Health, Faculty of Agriculture and Environmental Science, Szent István University Please ask the editor of the journal.

5. 5 Technical University of Budapest Institute of General & Analitical Chemistry 1521 Budapest, Hungary

6. 6 Department of Animal Physiology and Health, Faculty of Agriculture and Environmental Science, Szent István University Please ask the editor of the journal.

7. 7 Department of Animal Physiology and Health, Faculty of Agriculture and Environmental Science, Szent István University Please ask the editor of the journal.

8. 8 Department and Clinic for Obstetrics and Reproduction, Faculty of Veterinary Science, Szent István University Budapest, Hungary

Abstract

Serum/plasma fructosamine (SeFa) concentration is a reliable indicator used in human diabetic control. Tests for monitoring the carbohydrate/energy metabolism of (farm) animals are less commonly performed in veterinary laboratories, since most of the reliable determinations, both automated and manual, are relatively expensive. The aim of this study was to develop a precise, money- (and time-) saving automated micro method for measuring SeFa. ELISA microplates (20 µL samples and 200 µL reagents) and an automatic microplate autoreader were used. The classical nitroblue tetrazolium (NBT) stain reagent solution of Johnson et al. (1982) was modified using a SIGMA reagent to render it stable for up to one year. SeFa concentrations measured by the new method in 30 human blood plasma samples were compared with values obtained by the standard (generally used) LaRoche kit procedure. Fifteen cow, 13 dog and 18 chicken plasma samples were assayed by the new automated ‘micro’ method as well as by the manual test tube ‘macro’ method commonly used earlier. The modified reagent was applied for both methods. The coefficient of correlation (r) between the results obtained by the two methods was consistently between 0.94 and 0.98 (p < 0.001).

Publisher

Akademiai Kiado Zrt.

Subject

General Veterinary

Reference17 articles.

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2. Nonenzymatic glucosylation of lysine residues in albumin.;J. Baynes;Meth. Enzymol.,1984

3. Determination of glycohaemoglobin levels in ketonuric and nonketonuric cows (Short communication).;L. Bárdos;Acta Vet. Hung.,1989

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