Microbore high-performance liquid chromatographic determination of cisapride in rat serum samples using column switching

For the determination of cisapride from serum samples, an automated microbo re high-performance liquid chromatographic method with column switching has been developed. After serum samples (100 mu l) were directly injected onto a Capcell Pak MF Ph-1 pre-column (10x4 mm I.D.), the deproteinization and concentration were carried out by acetonitrile-phosphate buffer (20 mM, pH 7.0) (2:8, v/v) at valve position A. At 2.6 min, the valve was switched to position B and the concentrated analytes were transferred from MF ph-1 pre- column to a C-18 intermediate column (35x2 mm I.D.) using washing solvent. By valve switching to position A at 4.3 min, the analytes were separated on a Capcell Pak C-18 UG 120 column (250x1.5 mm I.D.) with acetonitrile-phosp hate buffer (20 mM, pH 7.0) (5:5, v/v) at a how-rate of 0.1 ml/min. Total a nalysis time per sample was 18 min. The linearity of response was good (r=0 .999) over the concentration range of 5-200 ng/ml. The within-day and day-t o-day precision (CV) and inaccuracy were less than 3.7% and 3.8%, respectiv ely. The mean recovery was 96.5+/-2.4% with the detection limit of 2 ng/ml. (C) 1999 Elsevier Science BN. All rights reserved.