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HPLC‐fluorescence assay for measuring mosapride in small volumes of rat plasma
Authors:Ching‐Ling Cheng  Ya‐Win Chang  Chen‐Hsi Chou
Affiliation:1. Department of Pharmacy, Chia‐Nan University of Pharmacy and Science, No. 60, Section 1, Erh‐Jen Road, Jen‐Te Shiang, Tainan county 71710, Taiwan;2. Institute of Clinical Pharmacy, Medical College, National Cheng Kung University, No. 1, University Road, Tainan 70101, Taiwan;3. Institute of Biopharmaceutical Sciences, Medical College, National Cheng Kung University, No. 1, University Road, Tainan 70101, Taiwan;4. Department of Pharmacy, National Cheng Kung University Hospital, No. 138, Sheng‐Li Road, Tainan 70403, Taiwan
Abstract:A simple and sensitive HPLC‐fluorescence assay was developed for the determination of a gastroprokinetic agent mosapride in small volumes of rat plasma. Samples (50 μL) were treated with 200 μL of the internal standard solution (cisapride, 0.1 μg/mL in acetonitrile). Chromatographic separation was achieved on a C18 column by gradient elution with the mobile phase of acetonitrile‐water containing 20 mM potassium dihydrogen phosphate, at a flow rate of 1 mL/min. Fluorescence was measured with excitation and emission set at 315 and 354 nm, respectively. The retention time was about 16 min for cisapride and 20 min for mosapride. No endogenous substances were found to interfere. The calibration curve was linear from 0.015 to 10 μg/mL. The lower limit of quantification was 0.015 μg/mL. The intra‐ and inter‐day precision expressed as relative standard deviation did not exceed 7.7%, and the accuracy was within 4.7% deviation of the nominal concentration. The method was used successfully to investigate the disposition kinetics of mosapride in rats. Copyright © 2009 John Wiley & Sons, Ltd.
Keywords:mosapride  gastroprokinetic agent  HPLC‐fluorescence  pharmacokinetics  rat
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