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Free fraction

From Wikipedia, the free encyclopedia
Pharmacokinetics parameter

Thefree fraction is a parameter inpharmacokinetics andreceptor-ligand kinetics.One speaks of two different free fractions:

  • Plasma free fraction, previously referred to as ƒ1,[1] is now referred to as ƒP according to consensusnomenclature.[2]
  • Tissue free fractionND), previously referred to as ƒ2[1]

Theplasma free fraction is the fraction of theligand at equilibrium inblood plasma that is not bound toplasma proteins.

See also

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References

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  1. ^abRoger N. Gunn; Steve R. Gunn; Federico E. Turkheimer;Vincent J. Cunningham (2002). "Positron Emission Tomography Compartmental Models: A Basis Pursuit Strategy for Kinetic Modeling".J. Cereb. Blood Metab.22 (4):1425–1439.doi:10.1097/00004647-200212000-00003.PMID 12468888.Table
  2. ^Innis, R.B.; Cunningham, VJ; Delforge, J; Fujita, M; Gjedde, A; Gunn, RN; Holden, J; Houle, S; et al. (2007)."Consensus nomenclature for in vivo imaging of reversibly binding radioligands".J Cereb Blood Flow Metab.27 (9):1533–1539.doi:10.1038/sj.jcbfm.9600493.PMID 17519979.

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