Liquid chromatographic analysis of disopyramide and its mono-N-dealkylated metabolite.
- 1 March 1979
- journal article
- research article
- Published by Oxford University Press (OUP) in Clinical Chemistry
- Vol. 25 (3) , 405-408
- https://doi.org/10.1093/clinchem/25.3.405
Abstract
We describe a rapid, sensitive, and specific "high performance" liquid chromatographic analysis for disopyramide and its mono-N-dealkylated metabolite in serum, urine, and saliva. We used a mu-Bondapak CN column and an acetate buffer mobile phase containing methanol. Retention times for the two compounds and the internal standard, p-chlorodisopyramide, were 3.4, 4.1, and 6.3 min, respectively. The lower limits of sensitivity for drug and metabolite were 50 and 80 micrograms/L, respectively, with maximum coefficients of variation of 4.6 and 12%, respectively. Currently used antiarrhythmic drugs did not interfere with the analysis of disopyramide, and the pharmacokinetics of the drug, obtained from studies of one subject, agree well with reported values.This publication has 5 references indexed in Scilit:
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- High-pressure liquid chromatographic analysis of drugs in biological fluidsJournal of Chromatography A, 1977
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- Relationship between the pharmacokinetics and pharmacodynamics of procainamideClinical Pharmacology & Therapeutics, 1976
- Rapid gas chromatographic determination of disopyamide in serum using a nitrogen detectorJournal of Chromatography A, 1975