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Human serum albumin-drug

Hanai, T., Miyazaki, R., and Kinoshita, T., Quantitative analysis of human serum albumin-drug interactions using reversed phase and ion-exchange liquid chromatography, Anal. Chim. Acta, 378, 77, 1999. [Pg.313]

Damsten, M.C., Commandeur, J.N.M., Fidder, A., Hulst, A.G.,Touw, D., Noort, D. and Vermeulen, N.P.E. (2007) Liquid chromatography/tandem mass spectrometry detection of covalent binding of acetaminophen to human serum albumin. Drug Metabolism and Disposition The Biological Fate of Chemicals, 35 (8), 1408-1417. [Pg.163]

Sjoholm, The specificity of drug binding sites on human serum albumin, Drug-Protein Binding (M. M. Reidenberg and S. Erill, eds,), Praeger, New York, 1986, p. 36. [Pg.357]

Bolze, S. Bromet, N. Gay-Eeutry, C. Massiere, E Boulieu, R. Hulot, T. Development of an In Vitro Screening Model for the Biosynthesis of Acyl Glucuronide Metabolites and the Assessment of Their Reactivity Toward Human Serum Albumin, Drug Metab. Dispos. 30,404 13 (2002). [Pg.312]

Bolze S, Bromet N, Gay-Feutry C, Massiere F, Boulieu R, Hulot T. Development of an in vitro screening model for the biosynthesis of acyl glucuronide metabolites and the assessment of their reactivity toward human serum albumin. Drug Metab Dispos 2002 30 404-413. [Pg.473]

Human Serum Albumin-Drug Binding Affinity Based on Liquid Chromatography... [Pg.19]

T. Hanai, Evaluation of measuring methods of human serum albumin-drug binding affinity, Curr. Pharm. Anal, 2007, 3, 205-212. [Pg.23]

T. Hanai, A. Koseki, R. Yoshikawa, M. Ueno, T. Kinoshita and H. Homma, Prediction of human serum albumin-Drug binding affinity without albumin. Anal. Chim. Acta, 2002, 454, 101-108. [Pg.51]

Table 18 Human serum albumin-drug binding affinity and drug properties. rrSTi represents log k measured using an immobilized-HSA phase. nKa represents predicted log hsa-represents log k of acidic compounds at pH 7.4. k represents log k of basic compounds at pH 7.4. MIFa and MIFb represents the molecular interaction energy values of acidic and basic compounds, resepectively. nKs represents log nST measured using a modified Hummel-Dreyer method. nJQ, nKs, nSTg and nKj represent values. PB and PB2 represent the binding %. Log Pc are predicted log P values, and log Pm are measured values. 7.4 represents pH 7.4. Reproduced by permission of Bentham Science, ref. 20. Table 18 Human serum albumin-drug binding affinity and drug properties. rrSTi represents log k measured using an immobilized-HSA phase. nKa represents predicted log hsa-represents log k of acidic compounds at pH 7.4. k represents log k of basic compounds at pH 7.4. MIFa and MIFb represents the molecular interaction energy values of acidic and basic compounds, resepectively. nKs represents log nST measured using a modified Hummel-Dreyer method. nJQ, nKs, nSTg and nKj represent values. PB and PB2 represent the binding %. Log Pc are predicted log P values, and log Pm are measured values. 7.4 represents pH 7.4. Reproduced by permission of Bentham Science, ref. 20.
Bischer, A. Iwaki, M. Zia-Amirhosseini, P Benet, L.Z. Stereoselective reversible binding properties of the gluciuonide conjugates of fenoprofen enantiomers to human serum albumin. Drug Metab.Dispos., 1996, 23, 900-903... [Pg.812]


See other pages where Human serum albumin-drug is mentioned: [Pg.44]    [Pg.368]    [Pg.65]   


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