Cross-linked iron dextran is an efficient oral phosphate binder in the rat
Author(s) -
Katharina Spengler,
Hartmut Follmann,
KarlSiegfried Boos,
D. Seidel,
F. von der Haar,
Robert Elsner,
F. Maywald
Publication year - 1996
Publication title -
nephrology dialysis transplantation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.654
H-Index - 168
eISSN - 1460-2385
pISSN - 0931-0509
DOI - 10.1093/ndt/11.5.808
Subject(s) - medicine , phosphate , phosphate binder , dextran , in vivo , in vitro , hydroxide , iron oxide , pharmacology , hyperphosphatemia , biochemistry , chemical engineering , calcium , inorganic chemistry , microbiology and biotechnology , chemistry , engineering , biology
BACKGROUNDThere is a need for alternative oral phosphate binders. In-vitro studies showed that iron(III)oxide-hydroxide-modified cross-linked dextran is a promising, insoluble phosphate-binding agent. The present study was designed to assess its in-vivo efficacy and safety in the rat.STUDY, DESIGN AND METHODSIron(III)oxide-hydroxide modified dextran beads were mixed with normal rat feed in a proportion of 8% by weight. With this formula rats were fed for 4 weeks. A control group received the same diet without added phosphate binder. Samples of blood, urine, and faeces were taken from each animal before the phosphate binder was administered, 2 weeks later, and at the end of the examination period (day 29). Phosphate, calcium, iron were analysed in the blood samples. Calcium and phosphate concentrations were determined in the urine, phosphate, calcium, and iron concentrations in the excrements. Stability of the material in the duodenum was also simulated.RESULTS AND CONCLUSIONSThe results demonstrate an excellent phosphate-binding capacity of the material and a good tolerance during the intestinal passage. No significant chemical or enzymatic degradation, histological alterations, or other treatment-related macroscopic findings were recorded. The present efficacy and toxicity study has shown effective phosphate binding with no toxicity and no iron release after ingestion of this novel phosphate binding agent. We propose clinical evaluation studies to assess whether similar efficacy and safety can be shown in humans.
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