Khosravi M J, Diamandis E P
CyberFluor Inc., Toronto, Canada.
Clin Chem. 1987 Nov;33(11):1994-9.
We describe a new "sandwich"-type non-isotopic immunoassay for human choriogonadotropin (hCG) in serum. In the assay, hCG is captured by a beta-subunit-specific monoclonal antibody, which is immobilized in a white microtiter well. The sandwich is completed by adding a second biotinylated monoclonal antibody specific for the whole hCG molecule. The degree of binding of biotinylated antibody, which is proportional to the amount of hCG present in the sample, is quantified by adding streptavidin labeled with the europium chelate 4,7-bis(chlorosulfophenyl)-1,10-phenanthroline-2,9-dicarboxylic acid (BCPDA), in the presence of excess Eu3+. The fluorescent complex formed on the solid-phase [monoclonal antibody-hCG-monoclonal antibody-biotin-streptavidin-BCPDA-Eu3+] is measured by excitation at 337.1 nm with a nitrogen laser and monitoring the emission at 615 nm in a specially designed gated fluorometer working in a time-resolved mode. A two-step procedure is proposed for routine use to avoid the "high-dose hook effect" of the simpler and faster one-step procedure. The hCG assay described has a dynamic range of 1 to 500 int. units/L, and is precise and accurate. Results agree well with those obtained with a commercially available immunoradiometric and a time-resolved immunofluorometric procedure.
我们描述了一种用于检测血清中人绒毛膜促性腺激素(hCG)的新型“夹心”式非同位素免疫测定法。在该测定法中,hCG被固定在白色微量滴定孔中的β亚基特异性单克隆抗体捕获。通过添加第二种针对完整hCG分子的生物素化单克隆抗体来完成夹心结构。在过量Eu3+存在的情况下,添加用铕螯合物4,7-双(氯磺苯基)-1,10-菲咯啉-2,9-二羧酸(BCPDA)标记的链霉亲和素,对与样品中hCG含量成正比的生物素化抗体的结合程度进行定量。在专门设计的以时间分辨模式工作的门控荧光计中,通过用氮激光在337.1nm处激发并监测615nm处的发射来测量在固相上形成的荧光复合物[单克隆抗体-hCG-单克隆抗体-生物素-链霉亲和素-BCPDA-Eu3+]。为避免更简单快速的一步法出现“高剂量钩效应”,提出了一种两步法用于常规检测。所描述的hCG测定法的动态范围为1至500国际单位/升,且精确准确。结果与用市售免疫放射测定法和时间分辨免疫荧光测定法获得的结果非常一致。