Kominami G, Yamauchi A, Ishihara S, Kono M
Steroids. 1981 Mar;31(3):303-14. doi: 10.1016/s0039-128x(81)90284-1.
A sensitive enzyme immunoassay for plasma betamethasone was developed using betamethasone-3-(O-carboxymethyl)oxime-beta-D-galactosidase conjugate as a labelled antigen and 4-methylumbelliferyl-beta-D-galactoside as a fluorescence substrate. The performances of the enzyme immunoassay were compared with that of a radioimmunoassay using 3H-betamethasone and the same antiserum. The minimal detectable level for the enzyme immunoassay was 0.15 pg/tube or 0.15 ng/ml of plasma, which was remarkably more sensitive than the radioimmunoassay level of 10 pg/tube or 2 ng/ml of plasma. The specificity was sufficient, in particular, the cross reactivity of cortisol as 0.008%. However, the precision of the enzyme immunoassay was inferior to that of the radioimmunoassay.
以倍他米松 -3-(O -羧甲基)肟-β -D -半乳糖苷酶结合物作为标记抗原,4 -甲基伞形酮基-β -D -半乳糖苷作为荧光底物,建立了一种用于检测血浆中倍他米松的灵敏酶免疫测定法。将该酶免疫测定法的性能与使用³H -倍他米松和相同抗血清的放射免疫测定法进行了比较。该酶免疫测定法的最低检测水平为0.15 pg/管或0.15 ng/ml血浆,比放射免疫测定法的10 pg/管或2 ng/ml血浆的检测水平明显更灵敏。其特异性足够,尤其是皮质醇的交叉反应率为0.008%。然而,该酶免疫测定法的精密度不如放射免疫测定法。