Berry M N, Mazzachi R D, Pejakovic M, Peake M J
Department of Biochemistry and Chemical Pathology, Flinders University of South Australia, Bedford Park.
Clin Chem. 1988 Nov;34(11):2295-8.
This is a kinetic assay for measuring serum Na+ concentration based on determination of Na+-dependent beta-galactosidase (EC 3.2.1.23) activity. The method, sufficiently sensitive to measure sub-millimolar concentrations of Na+, was modified by including a Na+-binding agent (cryptand) to provide a linear assay for serum Na+ concentrations between 110 and 160 mmol/L. The assay was developed with and evaluated in the Cobas Fara centrifugal analyzer (and has been used in other kinetic analyzers). Within-run and between-run CVs were less than 1%. The reaction rate for normal serum samples (0.20 delta A/min) is about 10-fold that of the reagent blank. Results correlated well with flame photometry. Interference from bilirubin, hemoglobin, lipemia, heparin, and other cations was negligible. The method offers a practical alternative to the use of ion-selective electrodes and flame photometry for measuring serum Na+ in high-throughput or "stat" biochemical analyzers.
这是一种基于测定钠依赖性β-半乳糖苷酶(EC 3.2.1.23)活性来测量血清钠浓度的动力学分析方法。该方法对测量亚毫摩尔浓度的钠具有足够的灵敏度,通过加入一种钠结合剂(穴醚)进行了改进,从而为110至160 mmol/L的血清钠浓度提供了一种线性分析方法。该分析方法是在Cobas Fara离心分析仪上开发并进行评估的(也已用于其他动力学分析仪)。批内和批间变异系数均小于1%。正常血清样本的反应速率(0.20吸光度变化/分钟)约为试剂空白反应速率的10倍。结果与火焰光度法相关性良好。胆红素、血红蛋白、脂血、肝素和其他阳离子的干扰可忽略不计。该方法为在高通量或“急诊”生化分析仪中测量血清钠提供了一种实用的替代离子选择性电极和火焰光度法的方法。