Labile iron in parenteral iron formulations: a quantitative and comparative study

被引:81
作者
Van Wyck, D
Anderson, J
Johnson, K
机构
[1] Univ Arizona, Coll Med, Tucson, AZ USA
[2] J2 Labs, Tucson, AZ USA
关键词
adverse effects; ferric gluconate; iron; iron dextran; iron sucrose; transferrin;
D O I
10.1093/ndt/gfg579
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Background. Evidence of iron-mediated oxidative stress. neutrophil dysfunction and enhanced bacterial growth after intravenous (IV) iron administration has been ascribed to a labile or bioactive iron fraction present in all IV iron agents. Methods. To quantify and compare the size of the labile fraction in several classes of IV iron agents, we examined iron donation to transferrin (Tf) in vitro. We added dilutions of ferric gluconate, iron sucrose and each of two iron dextran preparations to serum in vitro, passed the resulting samples through alumina columns to remove iron agent and free organic iron, and measured Tf-bound iron in the resulting eluates. Comparing results to serum samples without added iron, we calculated delta Tf-bound iron for each agent at each concentration. Finally, we compared delta Tf-bound iron to the concentration of added agent and calculated the percent iron donation to Tf. Results. We found that Tf-bound iron increased with added iron concentration for each agent: delta Tf-bound iron was directly related to the concentration and type of iron agent (P < 0.001). Mean percent iron donation to Tf ranged from 2.5 to 5.8% with the following progression: iron dextran-Dexferrum((R)) < iron dextran-INFeD(R) < iron sucrose < ferric gluconate. Pairwise differences between agents for percent iron donation were statistically significant (P<0.05) only between ferric gluconate and both iron dextran agents. and between iron sucrose and iron dextran-Dexferrum((R)). Conclusions. Approximately 2-6% of total iron in commonly used IV iron compounds is available for in vitro iron donation to Tf. This fraction may contribute to evidence of bioactive iron in patients after IV iron administration.
引用
收藏
页码:561 / 565
页数:5
相关论文
共 19 条
  • [1] Issues related to iron replacement in chronic kidney disease
    Agarwal, R
    Warnock, D
    [J]. SEMINARS IN NEPHROLOGY, 2002, 22 (06) : 479 - 487
  • [2] Pharmacokinetics and red cell utilization of 52Fe/59Fe-labelled iron polymaltose in anaemic patients using positron emission tomography
    Beshara, S
    Sörensen, J
    Lubberink, M
    Tolmachev, V
    Långström, B
    Antoni, G
    Danielson, BG
    Lundqvist, H
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 2003, 120 (05) : 853 - 859
  • [3] Pharmacokinetics and red cell utilization of iron(III) hydroxide-sucrose complex in anaemic patients:: a study using positron emission tomography
    Beshara, S
    Lundqvist, H
    Sundin, J
    Lubberink, M
    Tolmachev, V
    Valind, S
    Antoni, G
    Långström, B
    Danielson, BG
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1999, 104 (02) : 296 - 302
  • [4] High-dose parenteral iron sucrose depresses neutrophil intracellular killing capacity
    Deicher, R
    Ziai, F
    Cohen, G
    Müllner, M
    Hörl, WH
    [J]. KIDNEY INTERNATIONAL, 2003, 64 (02) : 728 - 736
  • [5] Labile iron in parenteral iron formulations and its potential for generating plasma nontransferrin-bound iron in dialysis patients
    Espósito, BP
    Breuer, W
    Slotki, I
    Cabantchik, ZI
    [J]. EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2002, 32 : 42 - 49
  • [6] Feldman HI, 2002, J AM SOC NEPHROL, V13, DOI 10.1681/ASN.V133734
  • [7] Sodium ferric gluconate complex in the treatment of iron deficiency for patients on dialysis
    Fishbane, S
    Wagner, J
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2001, 37 (05) : 879 - 883
  • [8] A randomized controlled trial of haemoglobin normalization with epoetin alfa in pre-dialysis and dialysis patients
    Furuland, H
    Linde, T
    Ahlmén, J
    Christensson, A
    Strömbom, U
    Danielson, BG
    [J]. NEPHROLOGY DIALYSIS TRANSPLANTATION, 2003, 18 (02) : 353 - 361
  • [9] Hoen B, 1998, J AM SOC NEPHROL, V9, P869
  • [10] JACOBS JC, 1990, CLIN CHEM, V36, P1803