کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1213081 | 1494124 | 2012 | 6 صفحه PDF | دانلود رایگان |
Pantoprazole (PAN), a selective proton pump inhibitor, is used clinically as a racemic mixture for the treatment of acid-related gastrointestinal disorders. To investigate its stereoselective pharmacokinetics, a chiral liquid chromatography–tandem mass spectrometry method was developed and validated to determine the pantoprazole enantiomers in dog plasma. After liquid–liquid extraction, a baseline resolution of enantiomers was achieved on an ovomucoid column using the mobile phase of methanol:acetonitrile:10 mM ammonium formate (pH 7) (10.4:2.6:87, v/v/v) at 30 °C within 10 min. Stable isotopically labeled (+)-d3-pantoprazole and (−)-d3-pantoprazole were used as internal standards. Acquisition of mass spectrometric data was performed in multiple reaction monitoring mode via positive atmospheric pressure chemical ionization. The method was linear in the concentration range of 20.0–10,000 ng/mL for each enantiomer using 25 μL of dog plasma. The lower limit of quantification (LLOQ) for each enantiomer was 20.0 ng/mL. Intra- and inter-day precision ranged from 3.2% to 10.3% for (+)-pantoprazole and 3.7–10.0% for (−)-pantoprazole. Accuracy varied from −1.4% to −0.2% for (+)-pantoprazole and −1.6% to 0.8% for (−)-pantoprazole. The validated method was applied successfully for stereoselective pharmacokinetic studies of racemic pantoprazole.
► A chiral LC–MS/MS method was validated to quantify pantoprazole enantiomers.
► Separation was performed on an ovomucoid protein column using MS compatible mobile phases.
► Baseline resolution within 10 min leads to a reduction in the overall analysis time.
Journal: Journal of Chromatography B - Volume 906, 1 October 2012, Pages 85–90