Poiesi C, Rodella A, Mantero G, Cannella G, Ferrari R, Albertini A
Department of Chemistry, School of Medicine, University of Brescia, Italy.
Clin Chem. 1989 Jul;35(7):1431-4.
We describe a radioimmunoassay (RIA) for measurement of atrial natriuretic peptide (ANP), based on one-step incubation and a simplified extraction procedure. The extraction was performed on a "Supelclean LC 18" column, with 2-mL plasma samples. Use of a diiodinated tracer improved the sensitivity of the RIA method. The minimal detectable value was 5 ng/L. Simplification of the extraction procedure and simultaneous incubation of the reagents provide a method more suitable for routine standard assay of ANP than those currently available. Intra- and interassay CVs were 6% (n = 12) and 11% (n = 10), respectively. The mean concentration of ANP in plasma of 32 healthy volunteers was 33 (SEM 4) ng/L. The ANP values for plasma after one-step incubation correlated well with those determined by a commercial RIA kit: r = 0.971, slope = 1.099, intercept = 1.949 ng/L (n = 25).
我们描述了一种用于测量心房利钠肽(ANP)的放射免疫分析(RIA)方法,该方法基于一步温育和简化的提取程序。提取在“Supelclean LC 18”柱上进行,使用2 mL血浆样本。使用二碘化示踪剂提高了RIA方法的灵敏度。最低检测值为5 ng/L。提取程序的简化以及试剂的同时温育提供了一种比现有方法更适合ANP常规标准检测的方法。批内和批间变异系数分别为6%(n = 12)和11%(n = 10)。32名健康志愿者血浆中ANP的平均浓度为33(标准误4)ng/L。一步温育后血浆的ANP值与商业RIA试剂盒测定的值相关性良好:r = 0.971,斜率 = 1.099,截距 = 1.949 ng/L(n = 25)。