EUROPIUM AND TERBIUM CHELATORS AS CANDIDATE SUBSTRATES FOR ENZYME-LABELED TIME-RESOLVED FLUOROMETRIC IMMUNOASSAYS

Thirty-three candidate fluorogenic chelators for Eu3+ and Tb3+ were examined. Ten were found to form highly fluorescent complexes with Eu3+ and five with Tb3+. In all cases, the fluorescence observed was lanthanide-specific, long-lived and was monitored by microsecond time-resolved fluorimetry. The fluorogenic chelators could be quantified, in the presence of an excess of lanthanide, at levels of < 1 x 10(-8) mol l-1 in all but one case. Two new fluorogenic chelators could form ternary complexes with Eu3+ and Tb3+, in the presence of ethylenediaminetetraacetic acid. The structures of the chelators identified are such that enzyme substrates could be developed and used for enzyme-labelled time-resolved fluorimetric immunoassays. It was found that one of the new chelators identified, 4-methylumbelliferyl phosphate, which forms fluorescent, long-lived complexes with Eu3+, could be split by alkaline phosphatase to phosphate and 4-methylumbelliferone, which does not form fluorescent complexes with Eu3+. Based on this, highly sensitive immunoassays for thyroid stimulating hormone and thyroxine in human serum were developed. It is anticipated that some of the identified chelators could be transformed into enzyme substrates suitable for highly sensitive, enzyme-labelled time-resolved fluorimetric immunoassays.