Free fraction
The free fraction is a parameter in pharmacokinetics and receptor-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 consensus nomenclature.[2]
- Tissue free fraction (ƒND), previously referred to as ƒ2[1]
The plasma free fraction is the fraction of the ligand at equilibrium in blood plasma that is not bound to plasma proteins.
See also[]
References[]
- ^ a b ; Steve R. Gunn; Federico E. Turkheimer; (2002). "Positron Emission Tomography Compartmental Models: A Basis Pursuit Strategy for Kinetic Modeling". 22 (4): 1425–1439. doi:10.1097/00004647-200212000-00003. PMID 12468888.Table
- ^ 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.
Others[]
- Milak MS, Severance AJ, Ogden RT, Prabhakaran J, Kumar JS, Majo VJ, Mann JJ, Parsey RV (2008). "Modeling Considerations for 11C-CUMI-101, an Agonist Radiotracer for Imaging Serotonin 1A Receptor In Vivo with PET". J. Nucl. Med. 49 (4): 587–596. doi:10.2967/jnumed.107.046540. PMC 3580231. PMID 18344443.
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