Pregled bibliografske jedinice broj: 72704
An automated immunoturbidimetric (Tina-quant HbA1c II) assay for HbA1c determination
An automated immunoturbidimetric (Tina-quant HbA1c II) assay for HbA1c determination // Clinical Chemistry and Laboratory Medicine. 39(2001), Special Supplement / Siest, Gérard (ur.).
Berlin: W. de Gruyter, 2001. str. S153-S153 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 72704 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
An automated immunoturbidimetric (Tina-quant HbA1c II) assay for HbA1c determination
Autori
Ruzić, Dragica ; Vrkić, Nada ; Tešija, Andrea ; Papić-Futač, Dalja ; Topić, Elizabeta
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Clinical Chemistry and Laboratory Medicine. 39(2001), Special Supplement
/ Siest, Gérard - Berlin : W. de Gruyter, 2001, S153-S153
Skup
Euromedlab 2001
Mjesto i datum
Prag, Češka Republika, 26.05.2001. - 31.05.2001
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
HBA1c; immunoassay methods; Olympus AU600
Sažetak
The aim of the study was to adapt an immunoassay (TINA-QUANT HBA1c, Roche Diagnostics, Mannheim) for the in vitro determination of hemoglobin A1c in whole blood on autoanalyzer Olympus AU 600, (Olympus Optical Co., Tokyo, Japan). Venous blood samples from diabetic patients are collected into vacutainer tubes K3EDTA containing. HBA1c determination is based on the turbidimetric inhibition immunoassay principle (TINIA), utilizing an antibody specific for the glycated aminoterminus of the hemoglobin beta-chain. Total hemoglobin concentration was determined in the second channel. Final result was calculated automatically. Calibration of the procedure was performed using internal HBA1c reference material. Imprecision within-run (on three different HbA1c concentrations), imprecision between-run (on triplicate for two control hemolysate measured ten days), and accuracy (with control material, and by comparison with ion- exchange low pressure liquid chromatography method, n=50) were assessed. Within-run and between-run imprecision CV was 0.88%-1.97% and 1.73%-4.34%, respectively. Results of the comparison study showed no statistical difference according to Passing & Bablok regression analysis (y=0.899x+1.16 ; r=0.989). Calibration of the assay was stable for at least 5 weeks, if the same lot of reagents was used. Refrigerated samples remained stable for HBA1c analysis for 7 days. Stability of the hemolysate was 3 hours at room temperature. Results of the study indicate that the automated immunoturbidimetric procedure adapted for Olympus AU600 autoanalyzer provides a precise and accurate determination of HBA1c.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Farmacija
POVEZANOST RADA
Projekti:
134003
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb,
KBC "Sestre Milosrdnice"
Profili:
Nada Vrkić
(autor)
Elizabeta Topić
(autor)
Dragica Ferenec-Ružić
(autor)
Andrea Tešija Kuna
(autor)