Effect of arsenosugar ingestion on urinary arsenic speciation
- 1 March 1998
- journal article
- research article
- Published by Oxford University Press (OUP) in Clinical Chemistry
- Vol. 44 (3) , 539-550
- https://doi.org/10.1093/clinchem/44.3.539
Abstract
We developed and evaluated a method for the determination of μg/L concentrations of individual arsenic species in urine samples. We have mainly studied arsenite [As(III)], arsenate [As(V)], monomethylarsonic acid (MMAA), and dimethylarsinic acid (DMAA) because these are the most commonly used biomarkers of exposure by the general population to inorganic arsenic and because of concerns over these arsenic species on their toxicity and carcinogenicity. We have also detected five unidentified urinary arsenic species resulting from the metabolism of arsenosugars. We combined ion pair liquid chromatography with on-line hydride generation and subsequent atomic fluorescence detection (HPLC/HGAFS). Detection limits, determined as three times the standard deviation of the baseline noise, are 0.8, 1.2, 0.7, and 1.0 μ/L arsenic for arsenite, arsenate, MMAA, and DMAA, respectively. These correspond to 16, 24, 14, and 20 pg of arsenic, respectively, for a 20-μL sample injected for analysis. The excellent detection limit enabled us to determine trace concentrations of arsenic species in urine samples from healthy subjects who did not have excess exposure to arsenic. There was no need for any sample pretreatment step. We used Standard Reference Materials, containing both normal and increased concentrations of arsenic, to validate the method. Interlaboratory studies with independent techniques also confirmed the results obtained with the HPLC/HGAFS method. We demonstrated an application of the method to the determination of arsenic species in urine samples after the ingestion of seaweed by four volunteers. We observed substantial increases of DMAA concentrations in the samples collected from the volunteers after the consumption of seaweed. The increase of urinary DMAA concentration is due to the metabolism of arsenosugars that are present in the seaweed. Our results suggest that the commonly used biomarkers of exposure to inorganic arsenic, based on the measurement of arsenite, arsenate, MMAA, and DMAA, are not reliable when arsenosugars are ingested from the diet.Keywords
This publication has 43 references indexed in Scilit:
- Single-Molecule electrophoresisAnalytical Chemistry, 1995
- Single molecule fluorescence burst detection of DNA fragments separated by capillary electrophoresisAnalytical Chemistry, 1995
- Speciation of arsenic compounds in some marine organismsEnvironmental Science & Technology, 1994
- Determination of arsenic species in fish by directly coupled high-performance liquid chromatography–inductively coupled plasma mass spectrometryJournal of Analytical Atomic Spectrometry, 1994
- Arsenic speciation in the environmentChemical Reviews, 1989
- The Metabolism of Arsenic in Humans Acutely Intoxicated by AS2O3. Its Significance for the Duration of BAL TherapyClinical Toxicology, 1981
- Guidelines for data acquisition and data quality evaluation in environmental chemistryAnalytical Chemistry, 1980
- Human retention studies with 74AsToxicology and Applied Pharmacology, 1980
- Clearance of arsenic ingested by man from arsenic contaminated fishBulletin of Environmental Contamination and Toxicology, 1979
- Metabolism of inorganic arsenic (74As) in humans following oral ingestionToxicology and Applied Pharmacology, 1979