Deeg R, Kraemer W, Ziegenhorn J
J Clin Chem Clin Biochem. 1980 Jan;18(1):49-52. doi: 10.1515/cclm.1980.18.1.49.
We have developed a kinetic fixed-time approach for the quantitative determination of serum glucose by use of the hexokinase/glucose-6-phosphate dehydrogenase method. To achieve a large measuring range, we have apparently increased the Michaelis constant of glucose-6-phosphate dehydrogenase through addition of the competitive inhibitor ATP. By this means, serum samples with glucose concentrations up to 55.5 mmol/l could be analyzed without pre-dilution. The method has been adapted to the ENI GEMSAEC analyzer and to the LKB 2086 Mark II analyzer. It yielded satisfactory results with regard to precision. A comparison of the kinetic procedure with the manual end-point method showed good agreement. No interferences from hemoglobin, bilirubin, or lipemia have been observed.
我们开发了一种动力学定时方法,用于通过己糖激酶/葡萄糖-6-磷酸脱氢酶法对血清葡萄糖进行定量测定。为了实现较大的测量范围,我们通过添加竞争性抑制剂ATP明显提高了葡萄糖-6-磷酸脱氢酶的米氏常数。通过这种方法,葡萄糖浓度高达55.5 mmol/l的血清样本无需预稀释即可进行分析。该方法已适配于ENI GEMSAEC分析仪和LKB 2086 Mark II分析仪。在精密度方面取得了令人满意的结果。动力学方法与手工终点法的比较显示出良好的一致性。未观察到血红蛋白、胆红素或脂血的干扰。