Liquid chromatography tandem mass spectrometry method for the quantification of Sarpogrelate, a selective 5‐HT 2A receptor antagonist, in plasma: application to a pre‐clinical pharmacokinetic study

• Published in: Biomedical chromatography 2010-11, Vol.24 (11), p.1159-1167
• Main Authors: Nirogi, Ramakrishna, Kandikere, Vishwottam, Mudigonda, Koteshwara, Ajjala, Devender, Suraneni, Ramakrishna, Thoddi, Parthasarathi
• Format: Article
• Language: English
• ISSN: 0269-3879; 1099-0801
• DOI: 10.1002/bmc.1422

A simple LC‐MS/MS method was developed and validated for the estimation of sarpogrelate in 50 µL of rat plasma. The analyte and internal standard (IS) were extracted from rat plasma by acetonitrile precipitation and they were separated on a reversed‐phase C 8 column with gradient program. The MS acquisition was performed with multiple reaction monitoring mode using m/z 430.2 to m/z 135.0 for analyte and m/z 448.2 to m/z 285.3 for IS. The calibration curves were linear over the range of 1–1000 ng/mL with the correlation coefficient greater than 0.999. With dilution integrity up to 20‐fold, the upper limit of quantification was extendable up to 15,000 ng/mL. The method was successfully applied to the analysis of rat plasma samples after single dose oral administration of sarpogrelate at 5 mg/kg to rats for the determination of its pharmacokinetics. Following oral administration the maximum mean concentration in plasma ( C max , 11514 ng/mL) was achieved at 0.25 h ( T max ) and the area under curve (AUC 0–24 ) was 11051 ± 3315 ng h/mL. The half‐life ( t 1/2 ) and clearance ( Cl ) were 2.9 ± 1.1 h and 490 ± 171 mL/h/kg, respectively. We believe that development of a method in rodent plasma would facilitate the ease of adaptability of sarpogrelate in human plasma. Copyright © 2010 John Wiley & Sons, Ltd.