Boyko W L, Russell H T
Obstet Gynecol. 1979 Dec;54(6):737-45.
An evaluation of a radioreceptor assay (RRA) for the quantitation of human chorionic gonadotropin (hCG) in serum resulted in intra- and interassay variations of 2.6 and 5.5% (average), respectively. Recovery of hCG in a preparation of second IRP-hCG gave an accuracy of 93.2%. Standard curve data demonstrated that variation in reagent addition and incubation time allowed for flexibility in the use of the assay depending on the level of sensitivity desired. The most sensitive assay, which used an incubation of 2 hours, gave a usable range of 40--250 mIU/ml hCG on the standard curve. The applicability of the quantitative RRA in clinical cases is shown with 9 patients (total of 31 serum samples) in a comparison study with a radioimmunoassay (RIA) for the beta-subunit of hCG.
对用于定量血清中人绒毛膜促性腺激素(hCG)的放射受体测定法(RRA)进行评估,结果显示该测定法的批内和批间变异分别为2.6%和5.5%(平均值)。在第二个国际参考品-hCG制剂中hCG的回收率为93.2%。标准曲线数据表明,根据所需的灵敏度水平,试剂添加量和孵育时间的变化使该测定法的使用具有灵活性。最灵敏的测定法孵育2小时,在标准曲线上hCG的可用范围为40--250 mIU/ml。在一项与hCGβ亚基放射免疫测定法(RIA)的比较研究中,9名患者(共31份血清样本)的临床病例显示了定量RRA的适用性。