1996
DOI: 10.1016/0009-8981(96)06349-8
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Specificity of hemoglobin A1c measurement by cation exchange liquid chromatography. Evaluation of a Mono S column method

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Cited by 23 publications
(14 citation statements)
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“…The Swedish DCM generates the lowest DCM HbA 1c values. The Mono S system, developed in 1983, shows an almost homogeneous HbA 1c peak in the chromatogram, but it contains carbamylated Hb as well as free ␣-globulin chains (25,31,32 ), so that the values are higher than those measured with the IFCC Reference Method. In contrast to the DCM methods, new dedicated HPLC systems are today eliminating many of these interfering adducts such as carbamylated Hb by use of more modern chromatographic material and improved gradients (33 ).…”
Section: Discussionmentioning
confidence: 99%
“…The Swedish DCM generates the lowest DCM HbA 1c values. The Mono S system, developed in 1983, shows an almost homogeneous HbA 1c peak in the chromatogram, but it contains carbamylated Hb as well as free ␣-globulin chains (25,31,32 ), so that the values are higher than those measured with the IFCC Reference Method. In contrast to the DCM methods, new dedicated HPLC systems are today eliminating many of these interfering adducts such as carbamylated Hb by use of more modern chromatographic material and improved gradients (33 ).…”
Section: Discussionmentioning
confidence: 99%
“…HbA1c was measured using the Mono-S method [12]. For conversion to measurements with the DCCT/NGSP method, the following conversion formula may be used: HbA1c (NGSP) (%) = 0.956 × HbA1c (Mono S) (%) + 1.182 (see e.g., http://www.hba1c.nu/).…”
Section: Methodsmentioning
confidence: 99%
“…HbA 1C was isolated and purified to homogeneity by cation-exchange chromatography on a column with Bio-Rex 70 pre-equilibrated with 50 mM potassium-phosphate buffer, pH 6.6 [26]. Before purification the labile glycohemoglobin fraction (pre-HbA 1C ), presented by Schiff base, was eliminated by addition of 20 volumes of sodium-acetate buffer, pH 5.5, with 0.1 mM NaCl to HbA 1C and incubation for 45 min at 37°C [27]. After that hemoglobin was dialyzed against 300 volumes of 50 mM potassium-phosphate buffer, pH 6.6, for 36 h with double buffer changing.…”
Section: Methodsmentioning
confidence: 99%