Review of paediatric gastrointestinal physiology data relevant to oral drug delivery

Jonathan L Kaye1

  • 1GlaxoSmithKline Pharmaceuticals, Harlow South, New Frontiers Science Park, Harlow, Essex CM19 5AW, UK. Jonathan.L.Kaye@gsk.com

Insights

Understanding gastrointestinal (GI) physiology in children is crucial for drug development. This review highlights age-related GI variations in paediatric populations, impacting oral drug absorption and pharmacokinetics.

Area of Science:

  • Pharmacology
  • Paediatric Physiology
  • Drug Development

Background:

  • European Union regulations necessitate paediatric population considerations in drug development.
  • Understanding paediatric gastrointestinal (GI) physiology is key to predicting oral drug pharmacokinetics.
  • Significant differences exist between adult and paediatric GI physiology, complicating drug absorption predictions.

Purpose of the Study:

  • To review and summarize publicly available data on paediatric GI physiology relevant to drug absorption.
  • To highlight age-dependent variations in GI physiology within the paediatric population.
  • To underscore the challenges in predicting oral drug pharmacokinetics in children.

Main Methods:

  • Literature search using EMBASE, MEDLINE (PubMed), and RIVM.
  • Inclusion of data from cited references and common physiology textbooks.
  • Focus on data from healthy paediatric individuals.

Main Results:

  • Collated and summarized data on GI pH and transit time in paediatric populations.
  • Observed a scarcity of data for younger paediatric age groups due to ethical considerations.
  • Identified significant variability in GI physiology within the paediatric population.

Conclusions:

  • Paediatric GI physiology, including pH and transit time, exhibits substantial age-related variability, particularly in the first month of life.
  • These physiological variations can significantly impact oral drug absorption.
  • The inherent variability and challenges in measurement underscore the complexity of paediatric drug development.
Abstract

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