A sensitive and specific assay for glycated albumin (GALE) has been developed. Ten pL of serum is fractionated by affinity chromatography on a boranateagarose column and quantitated by radioimmunoassay (RIA). Assay linearity is 15.6-1,000 ng of albumin. Dose-response curves prepared from both glycat
Lectin-Based Estimation of Glycated Hemoglobin in Diabetes Mellitus
โ Scribed by Pranab S. Basu; Sudip Chatterji; Sandip K. Batabyal
- Publisher
- John Wiley and Sons
- Year
- 2012
- Tongue
- English
- Weight
- 510 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0887-8013
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โฆ Synopsis
This study was undertaken to distinguish between normal and diabetic subjects by lectin-glycated hemoglobin interaction. The quantitative precipitin method was performed for the interaction between glucosespecific lectin Concanavalin A (Con A) and the glucose-containing RBC-lysate for the estimation of calculated HbA1c% from a standard curve. The standard curve was prepared by plotting the optical density of the precipitin for the interaction of standard HbA1c concentration with Con A against HbA1c reference standard. The absorbance range of the precipitate was 0.14-0.20 in normal subjects and the corresponding calculated HbA1c% along with plasma glucose (mg/dl) levels was 4.1-5.8% and 82-101 mg/dl respectively. Higher absorbance values, 0.22-0.42, were obtained in diabetic patients when the calculated HbA1c% was 6.3-12.2% and plasma glucose level was 120-292 mg/dl. Almost similar results were observed for HbA1c% (6.1-11.9%) of the same diabetic samples measured by conventional ion-exchange high performance liquid chromatography (HPLC). Excellent correlation coefficients of the two methods from regression analysis graph for normal (r = 0.98) and diabetic patients (r = 0.99) were observed. Furthermore, nondiabetic and diabetic hemoglobin variant subjects showed similar HbA1c% by our lectin-based assay when compared with standard HPLC method. We conclude that this lectin-based assay may be adopted to estimate glycated hemoglobin level in differentiating between normal and diabetic patients. This assay offers a good correlation with standard HPLC method. Moreover; the method is convenient, cheap, and needs no sophisticated instruments.
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