Stenman U H, Pesonen K, Ylinen K, Huhtala M L, Teramo K
J Chromatogr. 1984 Aug 3;297:327-32. doi: 10.1016/s0021-9673(01)89052-x.
We have developed a rapid chromatographic method for determination of glycosylated haemoglobins by high-performance liquid chromatography with a new cation-exchange column. The haemoglobins are eluted with a three-step gradient in 7 min, and total assay time including re-equilibration of the column is 15 min. The method permits separation and quantitation of HbAlc, even in the presence of elevated levels of HbF. HbA1a, A1b and A2 can also be determined. The results correlate well (r = 0.94) with those obtained by the macro-column method of Trivelli et al. [New Engl. J. Med., 284 (1971) 353] for determination of HbA1c. The method has been fully automated by the use of an automatic injector. The within-assay and between-assay coefficient of variation of the method is 2-3%.
我们开发了一种快速色谱法,通过使用新型阳离子交换柱的高效液相色谱法来测定糖化血红蛋白。血红蛋白在7分钟内通过三步梯度洗脱,包括柱再平衡在内的总分析时间为15分钟。该方法即使在HbF水平升高的情况下也能分离和定量HbAlc。HbA1a、A1b和A2也可以测定。结果与Trivelli等人[《新英格兰医学杂志》,284 (1971) 353]用于测定HbA1c的大柱法所得结果相关性良好(r = 0.94)。该方法通过使用自动进样器实现了完全自动化。该方法的批内和批间变异系数为2 - 3%。