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Comparison of digoxin and medigoxin in normal subjects.
Author(s) -
Hayward RP,
Greenwood H,
Hamer J
Publication year - 1978
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1111/j.1365-2125.1978.tb01686.x
Subject(s) - digoxin , radioimmunoassay , digitalis , volunteer , urine , chemistry , digitoxin , pharmacokinetics , endocrinology , medicine , glycoside , chromatography , pharmacology , heart failure , biology , stereochemistry , agronomy
1 The properties of a recently introduced digitalis glycoside, 4‐beta‐ methyl digoxin (medigoxin) were compared to those of a standard digoxin preparation. Using a radioimmunoassay (RIA) technique, serial plasma levels were recorded for 8 h following a single oral dose in five fasting volunteer subjects, and urinary glycoside elimination was measured for 4 consecutive days after dosage by use of a modification of the RIA method. 2 It was found that this RIA was suitable for plasma level measurement of both digoxin and midigoxin by reference to appropriate standard curves. Comparison of the plasma level profiles of these two drugs showed that medigoxin was very rapidly absorbed with peak levels occurring within 15–30 min, while digoxin produced peak levels after 45–75 min. The area under the plasma level‐time curve produced by medigoxin was also consistently greater than that produced by digoxin, even though the medigoxin dose used was smaller. Quantitative comparison of these areas after adjustment to compensate for differing doses showed that medigoxin is considerably more biologically available than digoxin under study conditions (ratio 1.6 +/− 0.25:1), and comparison of quantitative urinary elimination suggested that medigoxin is eliminated in the urine to a lesser extent than digoxin and therefore it undergoes more metabolism and/or hepato‐ biliary elimination.