Pegylated interferon-alpha2a kinetics during experimental haemodialysis: impact of permeability and pore size of dialysers

Aliment Pharmacol Ther. 2004 Jul 1;20(1):37-44. doi: 10.1111/j.1365-2036.2004.02014.x.

Abstract

Background: Therapeutics in end-stage renal disease (ESRD) patients undergoing haemodialysis (HD) has to consider potential drug clearance during the dialysis procedure. Pegylated interferon-alpha (PEG-IFN-alpha), a middle-size protein drug active against viral hepatitis, allows convenient once-weekly dosing due to prolonged plasma half-life.

Aim: To investigate the impact of permeability and dialyser pore size on PEG-IFN-alpha blood levels during experimental HD.

Methods: Polymethylmetacrylate (PMMA) membrane 1.6 m2 dialysers with three different permeabilities/pore sizes were selected.

Results: A 40 kDa PEG-IFN-alpha2a (PEGASYS) was not cleared (< 5%) through low-flux/small pore size (25 A;B3A) and high-flux/middle-large pore size (60 A;BKP) dialysers, and was partially (approximately 15%) through intermediate permeability/large pore size (100 A;BKF) dialysers. In contrast, unmodified 17 kDa IFN-alpha2a(Roferon-A) was removed (65%-95%) through BKP or BKF, but not B3A, PMMA dialysers. Moreover, 12 kDa PEG-IFN-alpha2b(PegIntron) was cleared (40%-80%) through PMMA dialysers with pore sizes > or = 60 angstroms. When B3A or BKP were replaced every hour PEG-IFN-alpha2a plasma levels remained constant throughout three experimental-HD-sessions, but PEG-IFN-alpha2b was cleared partially every BKP replacement. Porosity differ among high-flux dialysers. Neither PEG-IFN-alpha2a nor PEG-IFN-alpha2b were removed after three HD sessions through (27/31/33 A) pore size polysulphone dialysers. Although PEG-IFN-alpha2a was not cleared through middle pore-size (43 A/AN69ST) polyacrylonitrile dialyser, PEG-IFN-alpha2b was partially removed.

Conclusions: The pharmacokinetics of Peg-IFN-alpha may vary in a patient on dialysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents / pharmacokinetics*
  • Enzyme-Linked Immunosorbent Assay
  • Filtration
  • Humans
  • Interferon alpha-2
  • Interferon-alpha / pharmacokinetics*
  • Permeability
  • Polyethylene Glycols / pharmacokinetics*
  • Polymethyl Methacrylate
  • Recombinant Proteins
  • Renal Dialysis* / instrumentation

Substances

  • Antiviral Agents
  • Interferon alpha-2
  • Interferon-alpha
  • Recombinant Proteins
  • Polyethylene Glycols
  • Polymethyl Methacrylate
  • peginterferon alfa-2a