Evrin P E, Jansson N O, Bergdahl A
Clin Chim Acta. 1986 Mar 16;155(2):151-7. doi: 10.1016/0009-8981(86)90276-7.
A turbidimetric immunochemical method has been developed for quantitation of serum-beta 2-microglobulin. The serum samples are pre-treated with polyethyleneglycol to decrease the background turbidity and a centrifugal analyzer is used for the absorbance measurements. The within-assay coefficient of variation was 4.6% when 58 serum samples with a mean value of 2.0 mg/l were analyzed in duplicate. The sensitivity of the method is below 0.5 mg/l. When serum samples were analyzed by both the turbidimetric method and a radioimmunoassay a correlation coefficient of 0.989 was obtained. The turbidimetric method is simple, cheap and has a high capacity which makes it suitable for routine determinations of serum beta 2-microglobulin in a clinical laboratory.
已开发出一种比浊免疫化学方法用于定量血清β2-微球蛋白。血清样本用聚乙二醇预处理以降低背景浊度,并使用离心分析仪进行吸光度测量。对58份平均值为2.0mg/l的血清样本进行双份分析时,批内变异系数为4.6%。该方法的灵敏度低于0.5mg/l。当用比浊法和放射免疫分析法对血清样本进行分析时,相关系数为0.989。比浊法简单、廉价且检测量大,适用于临床实验室常规测定血清β2-微球蛋白。