@article {Mandula667, author = {Haritha Mandula and Jagan Mohan R. Parepally and Rose Feng and Quentin R. Smith}, title = {Role of Site-Specific Binding to Plasma Albumin in Drug Availability to Brain}, volume = {317}, number = {2}, pages = {667--675}, year = {2006}, doi = {10.1124/jpet.105.097402}, publisher = {American Society for Pharmacology and Experimental Therapeutics}, abstract = {Many studies have reported greater drug uptake into brain than that predicted based upon existing models using the free fraction (fu) of drug in arterial serum. To explain this difference, circulating plasma proteins have been suggested to interact with capillary membrane in vivo to produce a conformational change that favors net drug dissociation and elevation of fu. Albumin, the principal binding protein in plasma, has two main drug binding sites, Sudlow I and II. We tested this hypothesis using drugs that bind selectively to either site I (warfarin) or site II (ibuprofen), as well as mixed ligands that have affinity for both sites (tolbutamide and valproate). Brain uptake was determined in the presence and absence of albumin using the in situ rat brain perfusion technique. Unidirectional brain uptake transfer constants (Kin) were measured and compared with those predicted using the modified Kety-Crone-Renkin model: Kin = F(1 {\textendash} e{\textendash}fu {\texttimes} PSu/F), where F is perfusion flow and PSu is the permeability-surface area product to free drug of brain capillaries. The results demonstrated good agreement between measured and predicted Kin over a 100-fold range in perfusion fluid albumin concentration using albumin from three different species (i.e., human, bovine, and rat), as well as whole-rat serum. Kin decreased in the presence of albumin in direct proportion to perfusion fluid fu with constant PSu. The results show that brain uptake of selected Sudlow site I and II ligands matches that predicted by the modified Kety-Crone-Renkin model with no evidence for enhanced dissociation. The American Society for Pharmacology and Experimental Therapeutics}, issn = {0022-3565}, URL = {https://jpet.aspetjournals.org/content/317/2/667}, eprint = {https://jpet.aspetjournals.org/content/317/2/667.full.pdf}, journal = {Journal of Pharmacology and Experimental Therapeutics} }