A heterogeneous enzyme-labeled immunometric assay for quantifying digoxin in serum or plasma was developed. The sample's drug reacts with an excess of an antidigoxin Fablsquo;-beta;-galactosidase monoconjugate and then the free monoconjugate is removed by polyacrylamide digitoxigenin-coupled beads; the beta;-galactosidase activity of the supernatant measured photometrically at 634 nm is directly proportional to the digoxin concentration in the sample. The assay shares the basic reagents for the immunological reaction with the Seralyzer dry-strip immunometric assay; the reagents for the indicator enzyme reaction were instead formulated in liquid form for use with common clinical analyzers. The test requires a two-point calibration (a 3.0 mu;g/L digoxin calibrator and a reagent blank). One sample can be assayed in sim;20 min; the assay range is from 0.3 to 5.0 mu;g/L. Dilution tests showed an average found/expected ratio of 100.6percnt;. Mean analytical recovery was 99.2percnt;. Overall coefficients of variation (CVs) (three replicates for 12 runs over 15 days; daily calibration) ranged from 4.9 to 10.0percnt; (Technicon RA-50) and from 2.5 to 10.0percnt; (Cobas Fara) for samples with digoxin concentrations of 4.7 to 0.5 mu;g/L. No interference was found by high levels of common analytes (bilirubin, triglycerides, hemoglobin, total protein, uric acid) or anticoagulants. Cross-reactivity by digoxin metabolites and structurally-related compounds was investigated. Good correlations were found with radioimmunoassay (RIA) (r= 0.986) and enzyme immunoassay (EIA) (r= 0.994). Thus, the assay is a specific, reliable, and convenient method for measuring digoxin in both small and large laboratories.
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