@article {SJ{\"O}HOLM767, author = {INGVAR SJ{\"O}HOLM and BO EKMAN and ANITA KOBER and INGRID LJUNGSTEDT-P{\r A}HLMAN and BIRGITTA SEIVING and TORGNY SJ{\"O}DIN}, title = {Binding of Drugs to Human Serum Albumin:}, volume = {16}, number = {3}, pages = {767--777}, year = {1979}, publisher = {American Society for Pharmacology and Experimental Therapeutics}, abstract = {Human serum albumin can be immobilized in spherical, macroporous microparticles of polyacrylamide of about 1 {\textmu}m in diameter with retention of its native properties. It has been shown that diazepam, digitoxin and warfarin independently bind to albumin and can conveniently be used as markers of three separate, discrete binding sites on albumin. A simple technique has been devised by which the capacity of about 140 drugs and other compounds to affect the binding of the radioactively labeled markers has been studied. Some drugs, e.g. antirheumatic drugs of the isopropionic acid-type, some antidiabetic agents, penicillin derivatives, benzodiazepines, tryptophan, dansylsarcosine, and suiphobromophthalein efficiently displace diazepam. Other drugs, e.g., some diuretics, sulpha drugs, phenytoin, salicylic acid and butazone derivatives, azapropazoe, bilirubin, and dansylamide displace warfarin. Displacement of digitoxin is less common. In some cases the binding of the markers is improved, e.g., tamoxifen increases the binding of warfarin. Both competitive and allosteric mechanisms are responsible for the changed binding of the markers. Some results suggest the presence of more than the three binding sites for drugs on the albumin surface studied with diazepam, digitoxin and warfarin. ACKNOWLEDGMENTS The skillful technical assistance from Mr. B{\"o}rje Berg, Miss Solveigh H{\"o}glund, Mrs. Elisabeth Tidare and Mrs. Linn{\'e}a Wallsten is gratefully acknowledged. We also thank the manufacturers and their Swedish representatives for supplying us with the drugs used.}, issn = {0026-895X}, URL = {https://molpharm.aspetjournals.org/content/16/3/767}, eprint = {https://molpharm.aspetjournals.org/content/16/3/767.full.pdf}, journal = {Molecular Pharmacology} }