In vitro, in vivo and in silico models of drug distribution into the brain

J Pharmacokinet Pharmacodyn. 2013 Jun;40(3):301-14. doi: 10.1007/s10928-013-9303-7. Epub 2013 Feb 13.

Abstract

Achieving sufficient brain penetration to elicit efficacy in humans is one of the most challenging tasks for scientists in CNS Drug Discovery. Substantial progress has been made in the past decade in understanding the factors influencing the rate and extent of brain distribution via a variety of in vivo, in vitro and in silico methodologies, and hence, predict their likelihood of success in man. This purpose of this review is to summarize the current approaches with a special focus on parameters related to free drug concentrations in brain which are the most pharmacologically relevant for the majority of CNS disease targets. Due to the dynamic and complex nature of this targeted organ, it is inevitable that these approaches have not been able to provide a fully comprehensive assessment of brain distribution and are expected to evolve further in the years to come.

Publication types

  • Review

MeSH terms

  • Animals
  • Brain / metabolism*
  • Cell Line
  • Central Nervous System Agents / blood
  • Central Nervous System Agents / chemistry
  • Central Nervous System Agents / pharmacokinetics*
  • Drug Discovery / methods*
  • Humans
  • Models, Biological*
  • Structure-Activity Relationship
  • Substrate Specificity
  • Tissue Distribution

Substances

  • Central Nervous System Agents