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  1. Quantitative Structure – Clearance Relationships of Acidic Drugs
  2. Quantitative structure—plasma protein binding relationships of acidic drugs
  3. Prediction of Steady-State Volume of Distribution of Acidic Drugs by Quantitative Structure–Pharmacokinetics Relationships
  4. Binding of Kebuzone to Human Serum Albumin Studied by High Performance Liquid Affinity Chromatography
  5. Molecular Basis of Sulindac Competition with Specific Markers for the Major Binding Sites on Human Serum Albumin
  6. Thermodynamic Characterization of the Binding Process of Sulindac to Human Serum Albumin
  7. Stability of some novel thymidine, 5-bromo-2′-deoxyuridine and 3′-azido-2′-3′-dideoxythymidine analogues
  8. Protein binding of some nonsteroidal anti-inflammatory drugs studied by high-performance liquid affinity chromatography
  9. Protein Binding of Piroxicam Studied by Means of Affinity Chromatography and Circular Dichroism
  10. Stereoselective binding of ketoprofen enantiomers to human serum albumin studied by high-performance liquid affinity chromatography
  11. Albumin binding sites studied by high-performance liquid affinity chromatography
  12. New mathematical approach for the evaluation of drug binding to human serum albumin by high-performance liquid affinity chromatography
  13. In vitro metabolism of galanthamine hydrobromide (Nivalin®) by rat and rabbit liver homogenate
  14. Reversed-phase liquid chromatography for the determination of galanthamine and its metabolites in human plasma and urine