Determination of plasma procainamide and N-acetylprocainamide concentration by high-pressure liquid chromatography.
Open Access
- 1 July 1977
- journal article
- research article
- Published by Oxford University Press (OUP) in Clinical Chemistry
- Vol. 23 (7) , 1318-1320
- https://doi.org/10.1093/clinchem/23.7.1318
Abstract
We describe a routine method for determining concentrations of the antiarrhythmic drug procainamide and its active metabolite, N-acetylprocainamide, in plasma. A simple extraction of 1.0 ml of plasma is followed by separation and chromatographic analysis by use of a column containing microparticulate silica. p-nitro-N-(2-diethylaminoethyl)benzamide hydrochloride was synthesized and used as the internal standard. Total chromatographic time is only 7 min. The day-to-day CV during three months of daily use was less than 4% of the mean for each compound, and we saw no deterioration in column performance during this time. Phenobarbital, phenytoin, lidocaine, primidone, methsuximide, quinidine, and their metabolites do not interfere.This publication has 3 references indexed in Scilit:
- Analysis for Procainamide and N-Acetyl Procainamide in Plasma or Serum by High-Performance Liquid ChromatographyClinical Chemistry, 1977
- Simultaneous quantification of procainamide and n-acetylprocainamide with high-performance liquid chromatographyJournal of Chromatography A, 1976
- Antiarrhythmic efficacy of N‐acetylprocainamide in patients with premature ventricular contractionsClinical Pharmacology & Therapeutics, 1976