Application of simultaneous dissolution-absorption apparatus for screening formulations before bioequivalence studies

• In: Poster Presentation
• At: Stockholm (Sweden) (2017)
• Type: Poster
• Poster code: P-C-061-Monday
• By: BORBáS, Enikő (Budapest University of Technology and Economics, Organic Chemistry and Technology, Budapest, Hungary)
• Co-author(s): Bálint Sinkó: Pion Inc., Billerica, MA, United States
  Enikő Borbás: Organic Chemistry and Technology, Budapest University of Technology and Economics, Budapest, Hungary
  Zsombor Kristóf Nagy: Organic Chemistry and Technology, Budapest University of Technology and Economics, Budapest, Hungary
  Konstantin Tsinman: Pion Inc., Billerica, MA, United States
  
• Abstract:

  Backgrounds

  For generic drug development traditional dissolution tests have been used in the pharmaceutical industry to compare performance of different drug product formulations before conducting bioequivalence studies, even though the in vivo predictive power of these tests are questionable. Namely, when a poorly water-soluble API is formulated

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