Analysis of stereoselective drug interactions with serum proteins by high-performance affinity chromatography: A historical perspective

Zhao Li, David S. Hage

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

The interactions of drugs with serum proteins are often stereoselective and can affect the distribution, activity, toxicity and rate of excretion of these drugs in the body. A number of approaches based on affinity chromatography, and particularly high-performance affinity chromatography (HPAC), have been used as tools to study these interactions. This review describes the general principles of affinity chromatography and HPAC as related to their use in drug binding studies. The types of serum agents that have been examined with these methods are also discussed, including human serum albumin, α1-acid glycoprotein, and lipoproteins. This is followed by a description of the various formats based on affinity chromatography and HPAC that have been used to investigate drug interactions with serum proteins and the historical development for each of these formats. Specific techniques that are discussed include zonal elution, frontal analysis, and kinetic methods such as those that make use of band-broadening measurements, peak decay analysis, or ultrafast affinity extraction.

Original languageEnglish (US)
Pages (from-to)12-24
Number of pages13
JournalJournal of Pharmaceutical and Biomedical Analysis
Volume144
DOIs
StatePublished - Sep 10 2017

Fingerprint

Drug interactions
Affinity chromatography
Drug Interactions
Affinity Chromatography
Blood Proteins
Pharmaceutical Preparations
Serum Albumin
Lipoproteins
Toxicity
Glycoproteins
Kinetics
Acids
Serum

Keywords

  • Drug-protein binding
  • High-performance affinity chromatography
  • Human serum albumin
  • Lipoproteins
  • Stereoselective interactions
  • α-Acid glycoprotein

ASJC Scopus subject areas

  • Analytical Chemistry
  • Pharmaceutical Science
  • Drug Discovery
  • Spectroscopy
  • Clinical Biochemistry

Cite this

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