M. Sasieta et P. Jimeno, EVALUATION OF 5 IMMUNOASSAYS FOR THE DETERMINATION OF DIGOXIN IN SERUM, European journal of clinical chemistry and clinical biochemistry, 34(11), 1996, pp. 935-940
Five immunoassays for the determination of digoxin have been evaluated
(Digoxin II, Abbott; Cedia Digoxin XL, Microgenics; Coat-a-Count Digo
xin, Diagnostic Procedure Corporation, DPC; ''On-line'' Digoxin, Roche
Diagnostic Systems; EMIT 2000 Digoxin, Syva). Four of them required n
o sample pre-treatment. The methods included a radioimmunoassay, fluor
oimmunoassay, two enzyme-immunoassays and a turbidimetric immunoassay;
the last three mentioned were adapted to the Cobas(R) Mira Plus. The
intra- and inter-assay precision was lower than 9%, except for Microge
nics. The calibration stability fluctuated from 120 days for Abbott to
27 days for the Poche test, 7 days for the Syva assay and 2 days for
Microgenics. The DPC test was not assayed for calibration stability. T
he interference from ''digoxin-like immunoreactive factor(s)'' differe
d according to the assay. The highest interference was seen with Abbot
t and Microgenics, and the lowest with the DPC test. The comparison am
ong all the methods offered values of ''r'' higher than 0.95 except be
tween Microgenics and Syva assays where ''r'' was 0.896. The results o
btained with Poche and Microgenics were higher than 12% of the remaini
ng assays.