Skoug J W, Pardue H L
Department of Chemistry, Purdue University, West Lafayette, IN 47907.
Clin Chem. 1988 Feb;34(2):309-15.
Here we describe a kinetic approach for quantification of the immunoglobulins (IgG, IgA, IgM) in all regions of the immunoprecipitin curve. We use centrifugal mixing and report results for maximum-velocity, two-point, and multipoint curve-fitting methods as well as the use of rate coefficients obtained from the curve-fitting process to differentiate among regions of excess antibody, equivalence, and excess antigen. We show that it is possible to quantify each immunoglobulin over a concentration range from a large excess of antibody to moderate excesses of antigen with a single set of measurements made on a single dilution of each sample. Results for standard additions of the immunoglobulins to pooled sera have relative standard deviations (coefficients of variation) in the range of 1% to 3%, with analytical recoveries in the range of 95% to 106%. Correlations among determined and reported values in individual sera are quite good, with slopes ranging from 0.86 to 1.03 and no intercepts differing from zero by more than two standard deviation units. Concentrations quantified in 14 pathological sera by the proposed method correlated well with concentrations quantified by a fluorescence immunoassay method.
在此,我们描述了一种动力学方法,用于定量免疫沉淀曲线所有区域中的免疫球蛋白(IgG、IgA、IgM)。我们采用离心混合,并报告最大速度、两点和多点曲线拟合方法的结果,以及使用从曲线拟合过程中获得的速率系数来区分抗体过量、等价和抗原过量区域。我们表明,通过对每个样品的单一稀释液进行一组测量,就有可能在从大量抗体过量到中等抗原过量的浓度范围内对每种免疫球蛋白进行定量。向混合血清中标准添加免疫球蛋白的结果,其相对标准偏差(变异系数)在1%至3%范围内,分析回收率在95%至106%范围内。个体血清中测定值与报告值之间的相关性相当好,斜率范围为0.86至1.03,且截距与零的差异不超过两个标准差单位。通过所提出的方法在14份病理血清中定量的浓度与通过荧光免疫测定法定量的浓度相关性良好。