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Quantification of Pantoprazole by High Performance Liquid Chromatography (Hplc) Method: In Vitro and in Vivo Applications Publisher



Emami J1 ; Rezazadeh M1 ; Kalani M1
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Authors Affiliations
  1. 1. Department of Pharmaceutics, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, IR, Iran

Source: Journal of Liquid Chromatography and Related Technologies Published:2014


Abstract

A simple, sensitive, and selective HPLC method with UV detection was developed and validated for quantitation of pantoprazole in enteric coated tablets, dissolution medium, and human plasma following simple liquid-liquid extraction. The separation was achieved on a μ-Bondapak C18 HPLC column using sodium hydrogen phosphate solution (0.01 M)/acetonitrile (60/40 v/v) at pH 7.4 ± 0.1, as the mobile phase at a flow rate of 1.5 mL/min. Omeprazole was used as the internal standard for analysis of plasma samples. The retention time for pantoprazole and omeprazole were 8.4 and 7 min, respectively. Calibration curve was linear in the range of 0.025-5 μg/mL of pantoprazole using human plasma with the average recovery of 85 ± 5%. Within-day and between-day precision and accuracy did not exceed 14.4% and 15.8%, respectively. The HPLC assay was performed isocratically on a reversed-phase column with UV detection. A limit of quantification of 25 ng/mL achieved in our study was approximately twenty times smaller than that of other reported methods. The assay was applied to the analysis of pantoprazole levels in plasma collected from healthy participants entered to the pharmacokinetic study of this drug. Copyright © 2014 Taylor & Francis Group, LLC.
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