The hexadentate hydroxypyridinonate TREN-(Me-3,2-HOPO) is a more orally active iron chelator than its bidentate analogue

Robert A. Yokel, Andrea M. Fredenburg, Patricia W. Durbin, Jide Xu, Mary Kay Rayens, Kenneth N. Raymond

Research output: Contribution to journalArticlepeer-review

42 Scopus citations

Abstract

Bidentate hydroxypyridinone chelators effectively complex and facilitate excretion of trivalent iron. To test the hypothesis that hexadentate chelators are more effective than bidentate chelators at low concentrations, urinary and biliary Fe excretions were determined in Fe-loaded rats before and after administration of a bidentate chelator, Pr-(Me-3,2-HOPO), or its hexadentate analogue, TREN-(Me-3,2-HOPO). The bidentate chelator slightly increased biliary Fe excretion in Fe-loaded rats after IV (90 μmol/kg) and PO (90 or 270 μmol/kg) administration, but chelation efficiency did not exceed 1%. The hexadentate chelator markedly increased biliary Fe excretion, achieving overall chelation efficiencies of 14% after IV administration of 30 μmol/kg and 8 or 3% after PO (30 or 90 μmol/kg) administration. The hexadentate chelator was significantly more effective than the bidentate chelator after IV injection and oral dosing. In chelator-treated Fe-loaded or saline-injected rats, >90% of the excreted Fe was in the bile. Oral TREN-(Me-3,2-HOPO), given to non-Fe-loaded rats, did not appreciably change Fe output, indicating that there was little Fe depletion in the absence of Fe overload. These results support the hypothesis that greater Fe chelation efficiency can be achieved with hexadentate than with bidentate chelators at lower, and presumably safer, concentrations. The results also demonstrate that TREN-(Me-3,2-HOPO) is a promising, orally effective, Fe chelator. (C) 2000 Wiley-Liss, Inc. and the American Pharmaceutical Association.

Original languageEnglish
Pages (from-to)545-555
Number of pages11
JournalJournal of Pharmaceutical Sciences
Volume89
Issue number4
DOIs
StatePublished - 2000

Bibliographical note

Funding Information:
Supported by funds from The Office of the Vice Chancellor for Research and Graduate Studies, University of Kentucky Medical Center, and NIH Grant DK 32999, University of California, Berkeley. We thank Kathryn A. Meurer for skillful assistance with the iron analysis and Constance Silva and Jean Wolslegel for assistance in preparing the manuscript.

Funding

FundersFunder number
National Institute of Diabetes and Digestive and Kidney DiseasesR01DK032999

    ASJC Scopus subject areas

    • Pharmaceutical Science

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