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Comparison of three methods for determination of glucose
Dohnal L., Kalousová M., Zima T.
Language English Country Czech Republic
- MeSH
- Electrochemical Techniques methods utilization MeSH
- Financing, Organized MeSH
- Calibration MeSH
- Clinical Laboratory Techniques utilization MeSH
- Blood Glucose isolation & purification MeSH
- Plasma chemistry metabolism MeSH
- Humans MeSH
- Blood Specimen Collection methods standards utilization MeSH
- Reference Standards MeSH
- Reproducibility of Results MeSH
- Spectrophotometry methods utilization MeSH
- Statistics as Topic MeSH
- Check Tag
- Humans MeSH
Study refers comparison of three methods for glucose determination – precision (repeatability, reproducibility), traceability to SRM 965a NIST, comparability in blood-pools and in patients' samples: Electrochemical determination on Super GL (DiaSys, Germany) in hemolyzate – GL method, spectrophotometric determination using hexokinase (Glucose System Reagent 800, Olympus) – HKL method – and using glucose dehydrogenase (Glucose Gluc-DH, EcolineS+, DiaSys, Germany) – GDL method – in hemolyzate. For showing differences between the concentration of glucose in hemolyzed blood and corresponding plasma, spectrophotometric determination using hexokinase in plasma was used (Glucose System Reagent 800, Olympus) – HKP method. Coefficients of variation characterizing precision under repeatability and reproducibility conditions are not higher than 3.0% for the GL method, 6.3% for the GDL method and 15.8% for the HKL method with low sensitivity. For glucose concentration less than 8 mmol/l, HKL tends to give lower results than GDL, and GL tends to give higher results than GDL. For glucose concentration about 2 mmol/l, the results of glucose in plasma – HKP method – tend to be significantly lower (by more than ten percent) than in corresponding total (hemolyzed) blood. HKL method can be reasonably used in a high number of parallel determinations. For glucose 8 mmol/l and lower, comparability of results given by HKL, GDL and GL methods gradually worsens, while for glucose between 8 and 34 mmol/l results of the three mentioned methods are well comparable.
Lit.: 9
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- $a Lit.: 9
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- $a Study refers comparison of three methods for glucose determination – precision (repeatability, reproducibility), traceability to SRM 965a NIST, comparability in blood-pools and in patients' samples: Electrochemical determination on Super GL (DiaSys, Germany) in hemolyzate – GL method, spectrophotometric determination using hexokinase (Glucose System Reagent 800, Olympus) – HKL method – and using glucose dehydrogenase (Glucose Gluc-DH, EcolineS+, DiaSys, Germany) – GDL method – in hemolyzate. For showing differences between the concentration of glucose in hemolyzed blood and corresponding plasma, spectrophotometric determination using hexokinase in plasma was used (Glucose System Reagent 800, Olympus) – HKP method. Coefficients of variation characterizing precision under repeatability and reproducibility conditions are not higher than 3.0% for the GL method, 6.3% for the GDL method and 15.8% for the HKL method with low sensitivity. For glucose concentration less than 8 mmol/l, HKL tends to give lower results than GDL, and GL tends to give higher results than GDL. For glucose concentration about 2 mmol/l, the results of glucose in plasma – HKP method – tend to be significantly lower (by more than ten percent) than in corresponding total (hemolyzed) blood. HKL method can be reasonably used in a high number of parallel determinations. For glucose 8 mmol/l and lower, comparability of results given by HKL, GDL and GL methods gradually worsens, while for glucose between 8 and 34 mmol/l results of the three mentioned methods are well comparable.
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