Improved Liquid Chromatographic Determination of Procainamide and N-Acetylprocainamide in Serum
- 1 June 1983
- journal article
- research article
- Published by Wolters Kluwer Health in Therapeutic Drug Monitoring
- Vol. 5 (2) , 235-238
- https://doi.org/10.1097/00007691-198306000-00016
Abstract
A liquid chromatographic method for the determination of procainamide (PA) and N-acetylprocainamide (NAPA) in serum has been developed. This method utilizes isocratic conditions, ambient temperature, and a conventional fixed-wavelength 280-nm detector. Sample pretreatment involves extraction of PA and NAPA, along with p-amino-N-(2-dipropylaminoethyl)-benzamide hydrochloride as internal standard, into an organic phase and reex-traction into an aqueous acidic phase. Using this sample pretreatment, interferences due to commonly used drugs are eliminated. The method accurately measures PA and NAPA to levels as low as I mg/L.Keywords
This publication has 3 references indexed in Scilit:
- Measurement of Procainamide and N-Acetylprocainamide in Serum by High-Performance Liquid ChromatographyClinical Chemistry, 1997
- Rapid determination of procainamide and its N‐acetyl derivative in human plasma by high‐pressure liquid chromatographyJournal of Pharmaceutical Sciences, 1977
- Analysis for Procainamide and N-Acetyl Procainamide in Plasma or Serum by High-Performance Liquid ChromatographyClinical Chemistry, 1977