Dextromoramide is a narcotic analgesic drug which has been said to be
clinically useful where rapid onset and short duration of action is re
quired. The present communication describes a modification of previous
high performance liquid chromatographic methods for determining plasm
a dextromoramide concentrations. The method described is sensitive, ac
curate and precise, with intra-assay CV's of 4.1%, 4.1% and 4.2% and b
etween-assay CV's of 2.9%, 2.4% and 3.9% at concentrations of 10, 100
and 1000 mu g/L, respectively. It has a limit of quantitation of 5 mu
g/L with a chromatographic run time of 8 min. Pharmacokinetic studies
in 2 patients given 5mg of dextromoramide intravenously are presented
as applications of this method. These studies showed a bi-exponential
decay of dextromoramide in plasma over 24h with terminal half-lives of
3.7 and 23.5h which resulted from variability in plasma dextromoramid
e clearance and distribution volumes.