Abstract
A new rapid method is presented for the detection and quantitation of valproic acid (dipropyl acetic acid), VPA, in biological fluids. The method involves a single microextraction of the familiar acid-tungstate filtrate for the isolation of VPA. No back extraction or cleanup steps are required. One-microliter portions of the microextract are injected on a short, 3% OV-225 glass column, maintained isothermally at 110°C. Detection is accomplished by a standard flame ionization detector. Quantitation is achieved and precision is maintained through the use of an internal standard (paramethadione) carried through the procedure.

This publication has 0 references indexed in Scilit: