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Quantification of pantoprazole in human plasma using LC-MS/MS for pharmacokinetics and bioequivalence study

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Abstract

A highly sensitive and rapid method for the analysis of pantoprazole in human plasma using liquid chromatography coupled to tandem electrospray ionization mass spectrometry was developed. The procedure involves a simple protein precipitation method with methyl alcohol and separation by RP-HPLC. Detection was performed by positive ion electrospray ionization in multiple reaction monitoring mode, monitoring the transitions m/z 384.1 → 200.0 and m/z 346.1 → 198.0, for quantification of pantoprazole and IS, respectively. The standard calibration curves showed good linearity within the range of 5–5,000 ng mL−1. The lower limit of quantitation (LLOQ) was about 5 ng mL−1. The extractive recovery of pantoprazole from the biological matrix was more than 77.58% and the matrix effect was complied with relevant provision. The intra-day accuracy of the drug containing serum samples was more than 92.19% with a precision of 0.79–5.36%. The inter-day accuracy was 85.49% or more, with a precision of 0.91–12.67%. Intra and inter-day accuracy of the assay at four concentrations were 97.9–98.2% with a precision of 4.2–13.9%. This method offered good precision and accuracy and was successfully applied to the pharmacokinetic and bioequivalence studies of 40 mg of enteric-coated pantoprazole in 20 healthy Chinese volunteers.

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Correspondence to Xue-Min Zhou.

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Li, Y., Ding, MJ., Ma, J. et al. Quantification of pantoprazole in human plasma using LC-MS/MS for pharmacokinetics and bioequivalence study. Eur J Drug Metab Pharmacokinet 35, 147–155 (2011). https://doi.org/10.1007/s13318-010-0018-5

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  • DOI: https://doi.org/10.1007/s13318-010-0018-5

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