Impact of Chiral Bioanalytical Methods on the Bioequivalence of Ibuprofen Products Containing Ibuprofen Lysinate and Ibuprofen Base

Alfredo García-Arieta, Juan Manuel Ferrero-Cafiero, Montse Puntes, Ignasi Gich, Susana Morales-Alcelay, Maite Tarré, X. Font, Rosa Maria Antonijoan

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3 Citations (Scopus)

Abstract

© 2016 Wiley Periodicals, Inc. The purpose was to assess the impact of the use of a chiral bioanalytical method on the conclusions of a bioequivalence study that compared two ibuprofen suspensions with different rates of absorption. A comparison of the conclusion of bioequivalence between a chiral method and an achiral approach was made. Plasma concentrations of R-ibuprofen and S-ibuprofen were determined using a chiral bioanalytical method; bioequivalence was tested for R-ibuprofen and for S-ibuprofen separately and for the sum of both enantiomers as an approach for an achiral bioanalytical method. The 90% confidence interval (90% CI) that would have been obtained with an achiral bioanalytical method (90% CI: C max: 117.69–134.46; AUC 0t : 104.75–114.45) would have precluded the conclusion of bioequivalence. This conclusion cannot be generalized to the active enantiomer (90% CI: C max : 103.36–118.38; AUC 0t : 96.52–103.12), for which bioequivalence can be concluded, and/or the distomer (90% CI: C max : 132.97–151.33; AUC 0t : 115.91–135.77) for which a larger difference was observed. Chiral bioanalytical methods should be required when 1) the enantiomers exhibit different pharmacodynamics and 2) the exposure (AUC or C max ) ratio of enantiomers is modified by a difference in the rate of absorption. Furthermore, the bioequivalence conclusion should be based on all enantiomers, since the distomer(s) might not be completely inert, in contrast to what is required in the current regulatory guidelines. In those cases where it is unknown if the ratio between enantiomers is modified by changing the rate of absorption, chiral bioanalytical methods should be employed unless enantiomers exhibit the same pharmacodynamics. Chirality 28:429–433, 2016. © 2016 Wiley Periodicals, Inc.
Original languageEnglish
Pages (from-to)429-433
JournalChirality
Volume28
Issue number5
DOIs
Publication statusPublished - 1 Jan 2016

Keywords

  • bioequivalence
  • enantiomer ratio
  • enantiomers
  • ibuprofen
  • regulatory requirements

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