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In vitro protein-binding characteristics of delavirdine and its N-dealkylated metabolite

  • SUNY Buffalo

Research output: Contribution to journalArticlepeer-review

14 Scopus citations

Abstract

This study was performed to determine delavirdine, protein-binding characteristics as well as those of its N-dealkylated metabolite (N-DLV). Initial studies of 36 μM delavirdine and 30 μM N-DLV in solutions of plasma, albumin 4 g%, alpha-1-acid glycoprotein (AAG) 100 mg% or immune globulin (IVIG) 5 g% were conducted. Delavirdine (12, 36 and 73 μM) and N-DLV (10, 30 and 60 μM) were then studied alone and in combination in plasma and various concentrations of albumin. Studies were done in triplicate using equilibrium dialysis. The mean delavirdine fraction unbound (f(u)) in plasma, albumin, IVIG and AAG was 0.013, 0.033, 0.752 and 0.912 while the mean f(u) of N-DLV in these same protein solutions was 0.139, 0.195, 0.329 and 0.359. In plasma and albumin, a greater f(u) was observed at higher delavirdine concentrations and no significant changes in f(u) were noted with the addition of N-DLV. An increase in delavirdine f(u) was noted as the albumin concentrations decreased. The f(u) of N-DLV increased significantly as the concentration of albumin decreased as well as with decreasing N-DLV concentration. The potential implications of extensive delavirdine binding to plasma proteins, primarily albumin, are discussed.

Original languageEnglish
Pages (from-to)81-89
Number of pages9
JournalAntiviral Research
Volume32
Issue number2
DOIs
StatePublished - Oct 1996

Keywords

  • Bisheteroarylpiperazine
  • Delavirdine
  • HIV
  • Pharmacokinetics
  • Protein binding
  • Reverse transcriptase inhibitor

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