Alfthan H
J Immunol Methods. 1986 Apr 17;88(2):239-44. doi: 10.1016/0022-1759(86)90011-6.
Earlier studies have demonstrated, that an extremely rapid and sensitive assay for human chorionic gonadotropin (hCG) can be obtained by utilizing time-resolved fluorometry in combination with an immunometric assay. In this assay 2 different monoclonal antibodies are used. One antibody, directed against the beta-subunit of hCG, is immobilized by coating onto a microtitre well whereas the other antibody is labelled with a europium chelate. This assay was compared with a similar assay, which differed only by using 125I instead of europium as a label. The results demonstrate, that the high sensitivity of the immunofluorometric assay was mainly the result of the high antibody concentration used since almost equal sensitivity was obtained using the same amounts of radiolabelled antibody. However, this implied the use of 10-100 times more radioactivity per tube than usually applied in immunoassays. For practical purposes the time-resolved immunofluorometric assay was superior because the measuring time was shorter and the reagents non-radioactive and stable.
早期研究表明,通过将时间分辨荧光测定法与免疫测定法相结合,可获得一种极其快速且灵敏的人绒毛膜促性腺激素(hCG)检测方法。在该检测方法中,使用了两种不同的单克隆抗体。一种针对hCG的β亚基的抗体,通过包被固定在微量滴定孔上,而另一种抗体则用铕螯合物标记。将该检测方法与一种类似的检测方法进行了比较,后者的唯一区别在于使用¹²⁵I而非铕作为标记。结果表明,免疫荧光测定法的高灵敏度主要是由于所用抗体浓度高,因为使用相同量的放射性标记抗体可获得几乎相同的灵敏度。然而,这意味着每管使用的放射性比免疫测定中通常使用的要高10 - 100倍。从实际应用角度来看,时间分辨免疫荧光测定法更具优势,因为其测量时间更短,且试剂无放射性且稳定。