Hemmilä I, Dakubu S, Mukkala V M, Siitari H, Lövgren T
Anal Biochem. 1984 Mar;137(2):335-43. doi: 10.1016/0003-2697(84)90095-2.
A nonisotopic immunoassay has been developed based on a sensitive detection of europium (III) in water solution using time-resolved fluorometry. The europium label is bound to the antibody with EDTA derivatives, either diazophenyl-EDTA-Eu or isothiocyanatophenyl-EDTA-Eu. After the immunometric assay has been completed the europium is preferably dissociated from the antibody at low pH and measured by time-resolved fluorescence in a micellar solution containing Triton X-100, beta-diketone, and a Lewis base. The detergent solubilizes the chelating compounds in the solution and excludes water from the fluorescent ligand-europium complex. Europium concentrations as low as 5 X 10(-14)M were measured using a 1-s counting time. The sensitivity of the immunoassay of rabbit IgG used as a model system was 25 pg/ml (6 pg/assay).
基于使用时间分辨荧光法对水溶液中铕(III)进行灵敏检测,已开发出一种非同位素免疫测定法。铕标记物通过EDTA衍生物(重氮苯基 - EDTA - 铕或异硫氰酸苯酯 - EDTA - 铕)与抗体结合。免疫测定完成后,铕最好在低pH值下从抗体上解离,并在含有 Triton X - 100、β - 二酮和路易斯碱的胶束溶液中通过时间分辨荧光进行测量。去污剂使溶液中的螯合化合物溶解,并将水排除在荧光配体 - 铕络合物之外。使用1秒计数时间可测量低至5×10(-14)M的铕浓度。用作模型系统的兔IgG免疫测定的灵敏度为25 pg/ml(6 pg/测定)。