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Mercury Binding to the Chelation Therapy Agents DMSA and DMPS and the Rational Design of Custom Chelators for Mercury
Clinical chelation therapy of mercury poisoning generally uses one or both of two drugsmeso-dimercaptosuccinic acid (DMSA) and dimercaptopropanesulfonic acid (DMPS), commercially sold as Chemet and Dimaval, respectively. We have used a combination of mercury LIII-edge X-ray absorption spectroscopy...
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Published in: | Chemical research in toxicology 2004-08, Vol.17 (8), p.999-1006 |
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Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Clinical chelation therapy of mercury poisoning generally uses one or both of two drugsmeso-dimercaptosuccinic acid (DMSA) and dimercaptopropanesulfonic acid (DMPS), commercially sold as Chemet and Dimaval, respectively. We have used a combination of mercury LIII-edge X-ray absorption spectroscopy and density functional theory calculations to investigate the chemistry of interaction of mercuric ions with each of these chelation therapy drugs. We show that neither DMSA nor DMPS forms a true chelate complex with mercuric ions and that these drugs should be considered suboptimal for their clinical task of binding mercuric ions. We discuss the design criteria for a mercuric specific chelator molecule or “custom chelator”, which might form the basis for an improved clinical treatment. |
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ISSN: | 0893-228X 1520-5010 |
DOI: | 10.1021/tx049904e |