Meriö L, Pettersson K, Lövgren T
Department of Biotechnology, University of Turku, Finland.
Clin Chem. 1996 Sep;42(9):1513-7.
We have performed a one-step all-in-one dual-label dry reagent time-resolved fluorometric assay measuring free and total prostate-specific antigen (PSA). All assay-specific components were predried in an ordinary microtitration well, including the Eu and Tb chelate-labeled monoclonal antibodies for the recognition of free and total PSA, respectively. Only the sample and assay buffer needed to be added. Optimally, equilibrium was reached in <15 min. New intrinsically fluorescent Eu and Tb chelates were used, which made it possible to read the fluorescence directly from the solid phase. The developed dual-label assay with the simple protocol is ideal for easy automation, as the reaction wells can be of alternative design. The performance characteristics are equivalent to those of the present state-of-the-art single-label assays. The detection limits for free and total PSA were 0.03 and 0.02 microg/L, respectively, and the assays were linear over the range tested (up to 300 microg/L).
我们进行了一项一步式一体化双标记干式试剂时间分辨荧光测定法,用于检测游离和总前列腺特异性抗原(PSA)。所有测定特异性成分均预先干燥在普通微量滴定孔中,包括分别用于识别游离和总PSA的铕(Eu)和铽(Tb)螯合物标记的单克隆抗体。只需加入样品和测定缓冲液。最佳情况下,在不到15分钟内即可达到平衡。使用了新型的具有固有荧光的铕和铽螯合物,这使得可以直接从固相读取荧光。所开发的具有简单方案的双标记测定法非常适合易于自动化,因为反应孔可以采用替代设计。其性能特征与当前最先进的单标记测定法相当。游离和总PSA的检测限分别为0.03和0.02微克/升,并且在测试范围内(高达300微克/升)测定呈线性。