Parker K M, England J D, Da Costa J, Hess R L, Goldstein D E
Clin Chem. 1981 May;27(5):669-72.
This colorimetric assay for glycosylated hemoglobin can be performed in 120 min with equipment available in most clinical laboratories. The glucose moiety of glycosylated hemoglobin is converted to 5-hydroxymethylfurfural by heating with oxalic acid for 60 min is an autoclave at 124 degrees C and 124 kPa (18 lb/in.2). The adduct formed by reacting 2-thiobarbituric acid with hydroxymethylfurfural is measured photometrically and results are expressed either as nanomoles of hydroxymethylfurfural or as fructose equivalents. Within-assay and between-assay coefficients of variation were less than 2% and less than 3%, respectively. Comparison of results for 50 patients' specimens as measured by the present assay and as analyzed for hemoglobin A1c by liquid chromatography showed excellent correlation (r = 0.98).
这种糖化血红蛋白的比色测定法可在120分钟内完成,使用大多数临床实验室都有的设备。糖化血红蛋白的葡萄糖部分通过在124℃和124千帕(18磅/平方英寸)的高压釜中与草酸加热60分钟转化为5-羟甲基糠醛。通过光度法测量2-硫代巴比妥酸与羟甲基糠醛反应形成的加合物,结果以羟甲基糠醛的纳摩尔数或果糖当量表示。批内和批间变异系数分别小于2%和小于3%。通过本测定法测量的50份患者标本的结果与通过液相色谱法分析血红蛋白A1c的结果进行比较,显示出极好的相关性(r = 0.98)。