Pegylated interferon-α2a kinetics during experimental haemodialysis:: impact of permeability and pore size of dialysers

被引:21
作者
Barril, G
Quiroga, JA
Sanz, P
Rodrìguez-Salvanés, F
Selgas, R
Carreño, V
机构
[1] Fdn Estudio Hepatitis Virales, Madrid 28015, Spain
[2] Hosp U Princesa, Dept Nephrol, Madrid, Spain
[3] Hosp U Princesa, Dept Biostat, Madrid, Spain
关键词
D O I
10.1111/j.1365-2036.2004.02014.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
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 m(2) 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 Angstrom;B3A) and high-flux/middle-large pore size (60 Angstrom;BKP) dialysers, and was partially (approximate to15%) through intermediate permeability/large pore size (100 Angstrom;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 kDaPEG-IFN-alpha2b(PegIntron) was cleared (40%-80%) through PMMA dialysers with pore sizes greater than or equal to 60 Angstrom. 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 Angstrom) pore size polysulphone dialysers. Although PEG-IFN-alpha2a was not cleared through middle pore-size (43 Angstrom/AN69ST) polyacrylonitrile dialyser, PEG-IFN-alpha2b was partially removed. Conclusions: The pharmacokinetics of Peg-IFN-alpha may vary in a patient on dialysis.
引用
收藏
页码:37 / 44
页数:8
相关论文
共 21 条
[1]   Rational design of a potent, long-lasting form of interferon:: A 40 kDa branched polyethylene glycol-conjugated interferon α-2a for the treatment of hepatitis C [J].
Bailon, P ;
Palleroni, A ;
Schaffer, CA ;
Spence, CL ;
Fung, WJ ;
Porter, JE ;
Ehrlich, GK ;
Pan, W ;
Xu, ZX ;
Modi, MW ;
Farid, A ;
Berthold, W .
BIOCONJUGATE CHEMISTRY, 2001, 12 (02) :195-202
[2]   A new polymethylmethacrylate membrane for hemodialysis [J].
Bonomini, M ;
Fiederling, B ;
Bucciarelli, T ;
Manfrini, V ;
Diilio, C ;
Albertazzi, A .
INTERNATIONAL JOURNAL OF ARTIFICIAL ORGANS, 1996, 19 (04) :232-239
[3]   A pharmacokinetic model for alpha interferon administered subcutaneously [J].
Chatelut, E ;
Rostaing, L ;
Grégoire, N ;
Payen, JL ;
Pujol, A ;
Izopet, J ;
Houin, G ;
Canal, P .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 1999, 47 (04) :365-371
[4]   Properties of membranes used for hemodialysis therapy [J].
Clark, WR ;
Gao, DY .
SEMINARS IN DIALYSIS, 2002, 15 (03) :191-195
[5]  
Clark WR, 2002, J AM SOC NEPHROL, V13, pS41
[6]   Computational flow modeling in hollow-fiber dialyzers [J].
Eloot, S ;
De Wachter, D ;
Van Tricht, I ;
Verdonck, P .
ARTIFICIAL ORGANS, 2002, 26 (07) :590-599
[7]  
Espinosa M, 2001, CLIN NEPHROL, V55, P220
[8]   Pegylated interferon-α2b:: Pharmacokinetics, pharmacodynamics, safety, and preliminary efficacy data [J].
Glue, P ;
Fang, JWS ;
Rouzier-Panis, R ;
Raffanel, C ;
Sabo, R ;
Gupta, SK ;
Salfi, M ;
Jacobs, S .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2000, 68 (05) :556-567
[9]   Single-dose pharmacokinetics and safety of pegylated interferon-α2b in patients with chronic renal dysfunction [J].
Gupta, SK ;
Pittenger, AL ;
Swan, SK ;
Marbury, TC ;
Tobillo, E ;
Batra, V ;
Sack, M ;
Glue, P ;
Jacobs, S ;
Affrime, M .
JOURNAL OF CLINICAL PHARMACOLOGY, 2002, 42 (10) :1109-1115
[10]   Pegylation - A novel process for modifying pharmacokinetics [J].
Harris, JM ;
Martin, NE ;
Modi, M .
CLINICAL PHARMACOKINETICS, 2001, 40 (07) :539-551