Assay for nipecotic acid in small blood samples by gas chromatography-mass spectroscopy.

An analytical method for nipecotic acid quantification in rat blood was developed utilizing a stable isotope internal standard and capillary gas chromatography–mass spectroscopy. The method involves a solid phase extraction step followed by a two-step derivatization. The analytes are separated by capillary gas chromatography and detected by selected ion monitoring of their base peaks at 180 and 185 m/z, respectively. The assay has a limit of detection (LOD) of 10ng/ml and a limit of quantification of 26ng/ml in 200μl of rat whole blood. The linear range of the assay covers from 26 to 6500ng/ml (r2=0.9996, n=9). The coefficient of variation was less than 10% at concentrations of 50, 1000 and 5000ng/ml. The assay was used to characterize the pharmacokinetics of R-(-)-nipecotic acid in a rat. R-(-)-nipecotic acid clearance was 4.2ml/min, its half-life was 1.5h and its volume of distribution at steady state was 325ml.